<?xml version='1.0' encoding='UTF-8'?><?xml-stylesheet href="http://www.blogger.com/styles/atom.css" type="text/css"?><feed xmlns='http://www.w3.org/2005/Atom' xmlns:openSearch='http://a9.com/-/spec/opensearchrss/1.0/' xmlns:georss='http://www.georss.org/georss'><id>tag:blogger.com,1999:blog-8830256984796565668</id><updated>2010-02-04T10:06:03.986+01:00</updated><title type='text'>D'Orland KEG Ltd.</title><subtitle type='html'></subtitle><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default'/><link rel='alternate' type='text/html' href='http://www.d-orland.com/default.htm'/><link rel='hub' href='http://pubsubhubbub.appspot.com/'/><link rel='http://schemas.google.com/g/2005#feed' type='application/atom+xml' href='http://www.d-orland.com/atom.xml'/><author><name>robin</name><uri>http://www.blogger.com/profile/08864172896575683100</uri><email>noreply@blogger.com</email></author><generator version='7.00' uri='http://www.blogger.com'>Blogger</generator><openSearch:totalResults>12</openSearch:totalResults><openSearch:startIndex>1</openSearch:startIndex><openSearch:itemsPerPage>25</openSearch:itemsPerPage><entry><id>tag:blogger.com,1999:blog-8830256984796565668.post-5671676652502948423</id><published>2010-02-04T09:54:00.003+01:00</published><updated>2010-02-04T10:06:03.992+01:00</updated><title type='text'>Assay Standards</title><content type='html'>Key Organics has launched the Bionet Assay Standard Collection; designed and sourced specifically to satisfy Bionet customer demand for small, screening sized quantities of specific assay standards for comparison testing and screening. This is in keeping with Key Organics' drive to consistently listen to customers' changing needs, providing reliable solutions to their problems.&lt;br /&gt;&lt;br /&gt;The Bionet Assay Standard Collection eliminates unnecessary wastage of cumbersome bulk quantities of active ingredients and saves customers' money by providing bespoke mg quantities according to individual requirements rather than a 'standard pack size'. The Bionet Assay Standard Collection contains a diverse selection of assay standards, including APIs, Peptides, Natural Products, Hormones and Metabolites. All are available in screening size quantities for research purposes. These compounds can be purchased as part of a Bionet screening/fragment compound order for one stop shop needs or they can be purchased individually. &lt;br /&gt;&lt;br /&gt;&lt;a href="http://www.d-orland.com/pdf/Assay%20Standards%200909.pdf"&gt;pdf/Assay%20Standards%200909.pdf&lt;/a&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/8830256984796565668-5671676652502948423?l=www.d-orland.com%2Fdefault.htm' alt='' /&gt;&lt;/div&gt;</content><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/5671676652502948423/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=8830256984796565668&amp;postID=5671676652502948423' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/5671676652502948423'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/5671676652502948423'/><link rel='alternate' type='text/html' href='http://www.d-orland.com/2010/02/assay-standards.html' title='Assay Standards'/><author><name>Christopher Kennedy</name><email>noreply@blogger.com</email><gd:extendedProperty xmlns:gd='http://schemas.google.com/g/2005' name='OpenSocialUserId' value='17498465332199955208'/></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-8830256984796565668.post-7063157450842011225</id><published>2009-10-14T09:36:00.001+01:00</published><updated>2009-10-14T09:37:41.840+01:00</updated><title type='text'>Chiral Resolving Agents</title><content type='html'>We have the following Chiral Resolving Agents available:&lt;br /&gt;&lt;br /&gt;(-)-Di-p-toluoyl-(L)-tartaric acid monohydrate / anhdyrous [32634-66-5]&lt;br /&gt;(+)-Di-p-toluoyl-(D)-tartaric acid monohydrate / anhydrous [32634-68-7]&lt;br /&gt;(-)-Dibenzoyl-(L)-tartaric acid monohydrate / anhydrous [2743-38-6]&lt;br /&gt;(+)-Dibenzoyl-(D)-tartaric acid monohydrate / anhydrous [17026-42-5]&lt;br /&gt;(+).Diacetyl-(L)-tartaric anhydride [6283-74-5]&lt;br /&gt;(-)-Di-o-toluoyl-(L)-tartaric acid monohydrate / anhydrous &lt;br /&gt;M-Toyl-(+)-gluatmic acid [4816-80-2]&lt;br /&gt;S-(+)-alpha methoxyphenylacetic acid [26164-26-1]&lt;br /&gt;&lt;br /&gt;Please contact us for further information!&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/8830256984796565668-7063157450842011225?l=www.d-orland.com%2Fdefault.htm' alt='' /&gt;&lt;/div&gt;</content><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/7063157450842011225/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=8830256984796565668&amp;postID=7063157450842011225' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/7063157450842011225'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/7063157450842011225'/><link rel='alternate' type='text/html' href='http://www.d-orland.com/2009/10/chiral-resolving-agents.html' title='Chiral Resolving Agents'/><author><name>Christopher Kennedy</name><email>noreply@blogger.com</email><gd:extendedProperty xmlns:gd='http://schemas.google.com/g/2005' name='OpenSocialUserId' value='17498465332199955208'/></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-8830256984796565668.post-5329222229401413721</id><published>2009-10-09T09:05:00.001+01:00</published><updated>2009-10-09T09:07:26.153+01:00</updated><title type='text'>Catalyst Kits from Johnson Matthey</title><content type='html'>Johnson Matthey offers a multitude of Catalyst Kits which are an excellent tool for your various research projects.  They contain a collection of novel catalysts, ligands and metal scavenging products. &lt;br /&gt;&lt;br /&gt;For more information please contact us!&lt;br /&gt;&lt;br /&gt;&lt;a href="http://www.d-orland.com/pdf/Catalyst%20kits.pdf"&gt;pdf/Catalyst%20kits.pdf&lt;/a&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/8830256984796565668-5329222229401413721?l=www.d-orland.com%2Fdefault.htm' alt='' /&gt;&lt;/div&gt;</content><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/5329222229401413721/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=8830256984796565668&amp;postID=5329222229401413721' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/5329222229401413721'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/5329222229401413721'/><link rel='alternate' type='text/html' href='http://www.d-orland.com/2009/10/catalyst-kits-from-johnson-matthey.html' title='Catalyst Kits from Johnson Matthey'/><author><name>Christopher Kennedy</name><email>noreply@blogger.com</email><gd:extendedProperty xmlns:gd='http://schemas.google.com/g/2005' name='OpenSocialUserId' value='17498465332199955208'/></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-8830256984796565668.post-8738053544472420763</id><published>2009-10-07T15:22:00.002+01:00</published><updated>2009-10-07T15:32:22.938+01:00</updated><title type='text'>Grignard Reagents</title><content type='html'>Pentagon's purpose built Grignard plant at Workington offers advanced capability in the manufacture of reagents and their downstream derivatives. In addition to a wide range of own products in standard solvents and concentrations we offer custom manufacture of downstream products utilising more concentrated solutions than could be commercially shipped.&lt;br /&gt;&lt;br /&gt;The Grignard plant in Workington has the following technology available:&lt;br /&gt;&lt;br /&gt;    *  4 – 4.5m3 GL and SS vessels&lt;br /&gt;    * Fully DCS controlled Temperature -15°C to 150°C&lt;br /&gt;    * Distillation unit with 26 theoretical plates&lt;br /&gt;    * Hastelloy filter dryer&lt;br /&gt;    * Bulk and drums&lt;br /&gt;&lt;br /&gt;A full list of the Grignard reagents which are available:&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;&lt;a href="http://www.d-orland.com/xls/Grs.xls"&gt;xls/Grs.xls&lt;/a&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/8830256984796565668-8738053544472420763?l=www.d-orland.com%2Fdefault.htm' alt='' /&gt;&lt;/div&gt;</content><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/8738053544472420763/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=8830256984796565668&amp;postID=8738053544472420763' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/8738053544472420763'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/8738053544472420763'/><link rel='alternate' type='text/html' href='http://www.d-orland.com/2009/10/grignard-reagents.html' title='Grignard Reagents'/><author><name>Christopher Kennedy</name><email>noreply@blogger.com</email><gd:extendedProperty xmlns:gd='http://schemas.google.com/g/2005' name='OpenSocialUserId' value='17498465332199955208'/></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-8830256984796565668.post-5909113800418279315</id><published>2009-10-06T21:23:00.001+01:00</published><updated>2009-10-06T21:25:24.376+01:00</updated><title type='text'>Palladium Catalysts for Alpha-arylation</title><content type='html'>Johnson Matthey has recently identified:&lt;br /&gt;(DtBPF) PdCl2   Pd-118&lt;br /&gt;(DtBPF) PdBr2   Pd-128&lt;br /&gt;as exceptional candidates for alpha-arylation of&lt;br /&gt;various ketones with a variety of aryl&lt;br /&gt;chlorides and aryl bromides.&lt;br /&gt; &lt;br /&gt; These catalysts:&lt;br /&gt;  -are commercially available from JM&lt;br /&gt;  -give excellent yield and selectivity&lt;br /&gt;  -are air stable&lt;br /&gt;  -perform with mild reaction conditions&lt;br /&gt;  -demonstrate minimal Pd leaching&lt;br /&gt;&lt;br /&gt;Learn more at:&lt;br /&gt;&lt;br /&gt;A Highly Practical and General Route for α-Arylations of ketones Using Bis-phosphinoferrocene-Based Palladium Catalysts&lt;br /&gt;Gabriela A. Grasa* and Thomas J. Colacot&lt;br /&gt;Org. Process Res. Dev., 2008, 12 (3), pp 522-529&lt;br /&gt;&lt;br /&gt;α-Arylation of Ketones Using Highly Active, Air-Stable (dtBPF)PdX2 (X - Cl, Br) Catalysts&lt;br /&gt;Gabriela A. Grasa and Thomas J. Colacot*&lt;br /&gt;Org. Lett., 2007 9 (26), pp 5489-5492&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/8830256984796565668-5909113800418279315?l=www.d-orland.com%2Fdefault.htm' alt='' /&gt;&lt;/div&gt;</content><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/5909113800418279315/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=8830256984796565668&amp;postID=5909113800418279315' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/5909113800418279315'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/5909113800418279315'/><link rel='alternate' type='text/html' href='http://www.d-orland.com/2009/10/palladium-catalysts-for-alpha-arylation.html' title='Palladium Catalysts for Alpha-arylation'/><author><name>Christopher Kennedy</name><email>noreply@blogger.com</email><gd:extendedProperty xmlns:gd='http://schemas.google.com/g/2005' name='OpenSocialUserId' value='17498465332199955208'/></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-8830256984796565668.post-2195659319912995644</id><published>2009-10-06T21:20:00.000+01:00</published><updated>2009-10-06T21:21:00.432+01:00</updated><title type='text'>Organozinc Halides</title><content type='html'>BASF is sponsoring an on-line seminar on organozinc reagents that&lt;br /&gt; can help pharmaceutical and chemical research chemists bring new&lt;br /&gt; products to market. The Web-based discussion is scheduled for&lt;br /&gt; October 27, and will be available at two different time slots to&lt;br /&gt; accommodate participants from North America, Europe and Asia.&lt;br /&gt;&lt;br /&gt; Organozinc compounds are selective reagents and represent a powerful&lt;br /&gt; tool for carbon-carbon bond forming reactions. Over the last&lt;br /&gt; decades, organozinc reagents have been widely used in the total&lt;br /&gt; synthesis of natural products, in medicinal chemistry as well as in&lt;br /&gt; asymmetric synthesis and catalysis. This presentation will cover&lt;br /&gt; recent developments of the Negishi cross coupling technology and&lt;br /&gt; applications of this novel transformation on scale.&lt;br /&gt;&lt;br /&gt; The seminar "Organozinc Halides in Organic Synthesis" will be&lt;br /&gt; presented by Dr. Andreas Leitner, Senior Research Scientist,&lt;br /&gt; Inorganics for BASF in North America at two live sessions:&lt;br /&gt;&lt;br /&gt;     * The first session begins at 5 a.m. Eastern Daylight Time (EDT)&lt;br /&gt;       or 10 a.m. Central European Time (CET), 2:30 p.m. in India,&lt;br /&gt;       and 6 p.m. in Japan and Korea&lt;br /&gt;     * The second session begins at 2 p.m. EDT, or 11 a.m. Pacific Time&lt;br /&gt;&lt;br /&gt;&lt;br /&gt; Registration for both sessions is available at&lt;br /&gt; _www.v-workshops.com/pby/basf_&lt;br /&gt; &lt;ttp://www.v-workshops.com/pby/basf/private/private.asp%22&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/8830256984796565668-2195659319912995644?l=www.d-orland.com%2Fdefault.htm' alt='' /&gt;&lt;/div&gt;</content><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/2195659319912995644/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=8830256984796565668&amp;postID=2195659319912995644' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/2195659319912995644'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/2195659319912995644'/><link rel='alternate' type='text/html' href='http://www.d-orland.com/2009/10/organozinc-halides.html' title='Organozinc Halides'/><author><name>Christopher Kennedy</name><email>noreply@blogger.com</email><gd:extendedProperty xmlns:gd='http://schemas.google.com/g/2005' name='OpenSocialUserId' value='17498465332199955208'/></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-8830256984796565668.post-5290004261980699028</id><published>2009-10-06T20:58:00.003+01:00</published><updated>2009-10-06T21:11:28.443+01:00</updated><title type='text'>Quinuclidine Intermediates</title><content type='html'>We have recently added a range of Quinuclidine Intermediates:&lt;br /&gt;&lt;br /&gt;3-Quinuclidinone Hcl [1193-65-3]&lt;br /&gt;2-Methylene-3-Quinuclidinone Hcl [207556-03-4]&lt;br /&gt;3-Quinuclidinol (base or Hcl)[1619-34-7]&lt;br /&gt;3-Aminoquinuclidine diHcl [6530-09-2]&lt;br /&gt;3-Chloromethylquinuclidine&lt;br /&gt;3-Hydroxyquinuclidine Cyanhdyride [6238-30-8]&lt;br /&gt;3-Acetoxyquinuclidine[827-61-2]&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/8830256984796565668-5290004261980699028?l=www.d-orland.com%2Fdefault.htm' alt='' /&gt;&lt;/div&gt;</content><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/5290004261980699028/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=8830256984796565668&amp;postID=5290004261980699028' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/5290004261980699028'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/5290004261980699028'/><link rel='alternate' type='text/html' href='http://www.d-orland.com/2009/10/quinuclidine-intermediates.html' title='Quinuclidine Intermediates'/><author><name>Christopher Kennedy</name><email>noreply@blogger.com</email><gd:extendedProperty xmlns:gd='http://schemas.google.com/g/2005' name='OpenSocialUserId' value='17498465332199955208'/></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-8830256984796565668.post-6437487538654262026</id><published>2007-09-25T16:13:00.000+01:00</published><updated>2007-12-07T14:50:27.529+01:00</updated><title type='text'>Grignard Reactions, Grignard Solvents and  Grignard Reagents from Pentagon Chemical Specialities, Penn Speciality Chemicals and Ferro Fine Chemicals</title><content type='html'>&lt;a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://www.d-orland.com/uploaded_images/Grignard-picture-704531.png"&gt;&lt;img style="margin: 0pt 10px 10px 0pt; float: left; cursor: pointer;" src="http://www.d-orland.com/uploaded_images/Grignard-picture-704528.png" alt="" border="0" /&gt;&lt;/a&gt;D'Orland supplies a wide range of Reagents and Solvents for Grignard Reactions from it's principals, Pentagon Chemical Specialities, Penn Speciality Chemicals and Ferro Fine Chemicals. Products available include &lt;a href="http://www.d-orland.com/pdf/Methfgrig.pdf"&gt;Methyl Tetrahydrofuran (2-Methyl THF, MeTHF)&lt;/a&gt; and &lt;a href="http://www.d-orland.com/doc/Butyl%20Diglyme%20for%20Grignards.doc"&gt;Butyl Diglyme (Diethylene Glycol Dibutyl Ether)&lt;/a&gt; as well as other &lt;a href="http://www.d-orland.com/pdf/Glymesandgrign.pdf"&gt;Glymes&lt;/a&gt; (Glycol Diethers) which both make for safer Grignards as well as full range of Grignard reagents including  &lt;a href="http://www.d-orland.com/doc/AllylMgCl%202M%20in%20THF%20%28A057%29.doc"&gt;Allyl Magnesium Chloride&lt;/a&gt;,  &lt;a href="http://www.d-orland.com/doc/BuMgCl%202M%20in%20THF%20%28B050%29.doc"&gt;Butyl Magnesium Chloride&lt;/a&gt;, &lt;a href="http://www.d-orland.com/doc/EtMgBr%201M%20in%20MTBE%20%28E036%29.doc"&gt;Ethyl Magnesium Bromide&lt;/a&gt;, &lt;a href="http://www.d-orland.com/doc/EtMgCl%20%282.8M%20in%20THF%29.doc"&gt;Ethyl Magnesium Chloride&lt;/a&gt;, &lt;a href="http://www.d-orland.com/doc/MeMgBr%201M%20in%20THF%20%28M033%29.doc"&gt;Methyl Magnesium Bromide&lt;/a&gt;, &lt;a href="http://www.d-orland.com/doc/MeMgCl%203M%20in%20THF%20%28M035%29%20Data%20Sheet.doc"&gt;Methyl Magnesium Chloride&lt;/a&gt;, &lt;a href="http://www.d-orland.com/doc/Phenyl%20Magnesium%20Chloride%201M%20in%20THF.doc"&gt;Phenyl Magnesium Chloride&lt;/a&gt;, &lt;a href="http://www.d-orland.com/doc/PhMgBr%20%282.8M%20in%20DEE%20-%20J%20Grade%29.doc"&gt;Phenyl Magnesium Bromide&lt;/a&gt;, &lt;a href="http://www.d-orland.com/doc/tertBuMgCl%20%282M%20in%20DEE%29.doc"&gt;Tert-Butyl Magnesium Chloride&lt;/a&gt; to name a few. These reagents are all available in various solvents, including Toluene, THF and Diethyl Ether, whilst we can also make the next step of the reation under contract. Please do no hesistate to contact us for further information.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/8830256984796565668-6437487538654262026?l=www.d-orland.com%2Fdefault.htm' alt='' /&gt;&lt;/div&gt;</content><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/6437487538654262026/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=8830256984796565668&amp;postID=6437487538654262026' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/6437487538654262026'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/6437487538654262026'/><link rel='alternate' type='text/html' href='http://www.d-orland.com/2007/09/grignard-reactions-and-grignard.html' title='Grignard Reactions, Grignard Solvents and  Grignard Reagents from Pentagon Chemical Specialities, Penn Speciality Chemicals and Ferro Fine Chemicals'/><author><name>Christopher Kennedy</name><email>noreply@blogger.com</email><gd:extendedProperty xmlns:gd='http://schemas.google.com/g/2005' name='OpenSocialUserId' value='17498465332199955208'/></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-8830256984796565668.post-8304712460398103233</id><published>2007-07-31T10:33:00.000+01:00</published><updated>2007-12-07T14:48:25.354+01:00</updated><title type='text'>Homogenous and Heterogenous Catalysts, Enzymes and Metathesis from Johnson Matthey</title><content type='html'>&lt;a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://www.d-orland.com/uploaded_images/Smop-fibre-detail-740414.jpg"&gt;&lt;img style="margin: 0pt 10px 10px 0pt; float: left; cursor: pointer;" src="http://www.d-orland.com/uploaded_images/Smop-fibre-detail-740412.jpg" alt="" border="0" /&gt;&lt;/a&gt;D'Orland represents Johnson Matthey Catalysts and Chiral Technologies in Hungary, Poland, The Czech and Slovak Republics as well as Croatia and Slovenia for their excellent range of Heterogenous, Homogenous, Sponge Nickel and Metal scavenging agents, the latter being marketed under the Smopex name.&lt;br /&gt;&lt;br /&gt;If a catalyst could be of interest for your rection, then please do not hesitate to contact us and we will endevour to recommend the ideal catalyst for the synthesis in question.&lt;br /&gt;&lt;br /&gt;There is also a wealth of information available to help with the correct choice of catalyst, be it a homogenous or heterogenous one. A good place to start is the &lt;a href="http://www.d-orland.com/pdf/handbk.pdf"&gt;catalyst technical handbook&lt;/a&gt; We can of course also post the very useful reaction guide to interested parties, but the &lt;a href="http://www.d-orland.com/pdf/Hetkit.pdf"&gt;Hetergenous  Screening Kit&lt;/a&gt; certainly should be part of any laboratory where catalysis is being looked at and every kit kit comes with an excellent reaction chart. That a number of factors can affect the performance of a catalyst and that a 5 % or 10 % Palladium on Carbon is not just that, is show on the following sheets concerning &lt;a href="http://www.d-orland.com/pdf/O.pdf"&gt;O-Debenzylation&lt;/a&gt;  and &lt;a href="http://www.d-orland.com/pdf/Npdf"&gt;N-Benzylation&lt;/a&gt;.&lt;br /&gt;&lt;br /&gt;For homogenous catalytic reactions the &lt;a href="http://www.d-orland.com/pdf/Coupl.pdf"&gt;Coupling Table&lt;/a&gt; should enable the choice of an ideal catalyst and again there is a &lt;a href="http://www.d-orland.com/pdf/Chiralkit.pdf"&gt;Chiral Coupling Kit&lt;/a&gt; available. Details of other homogenous catalytic reactions using &lt;a href="http://www.d-orland.com/pdf/Hpre.pdf"&gt;rhodium, iridium and ruthernium&lt;/a&gt; are can be downloaded as well as information on &lt;a href="http://www.d-orland.com/pdf/Ch.pdf"&gt;Chiral Technologies&lt;/a&gt;&lt;span style="text-decoration: underline;"&gt;&lt;/span&gt; for carbon - oxygen and carbon nitrogen coupling reactions.&lt;br /&gt;&lt;br /&gt;There is of course also more information on the fourth generation of coupling catalysts, where Pd-118 ( Dichloro [1,1'-bis (di-tert butyl-phosphino) ferrocene] Palladium (II) ) could be of particular interest due to the fact that it is both air and moisture stable enabling some reactions to be carried out in a mixture of water and ethanol and avoiding the need for the catalyst to be stored in a glove box.&lt;br /&gt;&lt;br /&gt;Johnson Matthey have also recently added a range of catalytic &lt;a href="http://www.d-orland.com/pdf/enz.pdf"&gt;enzymes&lt;/a&gt; to their range, which show high enantiouselectivity particularly for ketone reductions.&lt;br /&gt;&lt;br /&gt;A range of &lt;a href="http://www.d-orland.com/pdf/Meta.pdf"&gt;Metathesis&lt;/a&gt; Catalysts has also been introduced recently and these do currently fall outside the scope of the patents on the Grubbs type catalysts.&lt;br /&gt;&lt;br /&gt;The good old tried and trusted &lt;a href="http://www.d-orland.com/ppt/smop.ppt"&gt;Sponge Metal Catalysts&lt;/a&gt; which are made by the Raney Process, are of course also available!&lt;br /&gt;&lt;br /&gt;Lastly, &lt;a href="http://www.d-orland.com/pdf/smop.pdf"&gt;Smopex&lt;/a&gt;® should not be forgotten and a short &lt;a href="http://www.d-orland.com/ppt/smop.ppt"&gt;presentation&lt;/a&gt; about Smopex illustrates why it should always be considered when a precious metal catalyst is used to recover as much of the palladium, platinum, ruthenium or rhodium as possible.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/8830256984796565668-8304712460398103233?l=www.d-orland.com%2Fdefault.htm' alt='' /&gt;&lt;/div&gt;</content><link rel='replies' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/8304712460398103233/comments/default' title='Post Comments'/><link rel='replies' type='text/html' href='https://www.blogger.com/comment.g?blogID=8830256984796565668&amp;postID=8304712460398103233' title='0 Comments'/><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/8304712460398103233'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/8304712460398103233'/><link rel='alternate' type='text/html' href='http://www.d-orland.com/2007/07/smopex.html' title='Homogenous and Heterogenous Catalysts, Enzymes and Metathesis from Johnson Matthey'/><author><name>Christopher Kennedy</name><email>noreply@blogger.com</email><gd:extendedProperty xmlns:gd='http://schemas.google.com/g/2005' name='OpenSocialUserId' value='17498465332199955208'/></author><thr:total xmlns:thr='http://purl.org/syndication/thread/1.0'>0</thr:total></entry><entry><id>tag:blogger.com,1999:blog-8830256984796565668.post-7805255332639181105</id><published>2007-04-16T11:43:00.000+01:00</published><updated>2007-12-07T14:53:20.227+01:00</updated><category scheme='http://www.blogger.com/atom/ns#' term='BASF'/><title type='text'>BASF Inorganics: Boron Reducing Agents for Assymetric Synthesis and Suzuki Coupling. Metal Alcoholates for Deprotonation.</title><content type='html'>&lt;a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://www.d-orland.com/uploaded_images/logo-1-700851.gif"&gt;&lt;img style="margin: 0pt 10px 10px 0pt; float: left; cursor: pointer;" src="http://www.d-orland.com/uploaded_images/logo-1-700845.gif" alt="" border="0" /&gt;&lt;/a&gt;D'Orland can offer a full range of Alkali Metal Deprotonating agents (such as &lt;a href="http://www.d-orland.com/pdf/ktb1.pdf"&gt;Potassium-Tert-Butoxide&lt;/a&gt;  and &lt;a href="http://www.d-orland.com/pdf/Statech.pdf"&gt;Sodium-Tert-Amylate&lt;/a&gt;), Boron Reducing Agents and Suzuki Cross-Coupling Reagents for the Croatian, Slovenian, Hungarian, Czech and Slovak markets.&lt;br /&gt;&lt;br /&gt;Furthermore Coreys Catalyst (Methyl Oxazaborolidine) is now available commercially and further information on the Corey Catalyst is on D'Orland's products page.&lt;br /&gt;&lt;br /&gt;An interesting presentation on Metal Alcoholates and Boron Reagents for Organic Synthesis is available &lt;a href="http://www.d-orland.com/pdf/Fiene%20presentation.pdf"&gt;here&lt;/a&gt; whilst a short presentation on Suzuki Cross Coupling Reagents is available &lt;a href="http://www.d-orland.com/pdf/suzukislides.ppt"&gt;here&lt;/a&gt;.&lt;br /&gt;&lt;br /&gt;Please do not hesitate to contact us for more information on these or any other BASF Inorganics Products.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/8830256984796565668-7805255332639181105?l=www.d-orland.com%2Fdefault.htm' alt='' /&gt;&lt;/div&gt;</content><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/7805255332639181105'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/7805255332639181105'/><link rel='alternate' type='text/html' href='http://www.d-orland.com/2007/04/basf-visit.html' title='BASF Inorganics: Boron Reducing Agents for Assymetric Synthesis and Suzuki Coupling. Metal Alcoholates for Deprotonation.'/><author><name>Christopher Kennedy</name><email>noreply@blogger.com</email><gd:extendedProperty xmlns:gd='http://schemas.google.com/g/2005' name='OpenSocialUserId' value='17498465332199955208'/></author></entry><entry><id>tag:blogger.com,1999:blog-8830256984796565668.post-5527300629873215300</id><published>2007-03-02T15:07:00.000+01:00</published><updated>2007-03-30T16:40:56.092+01:00</updated><title type='text'>High Purity Organic Bases</title><content type='html'>&lt;a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://www.engr.utexas.edu/che/students/images/austin-1.jpg"&gt;&lt;img style="margin: 0pt 10px 10px 0pt; float: left; cursor: pointer; width: 271px; height: 204px;" src="http://www.engr.utexas.edu/che/students/images/austin-1.jpg" alt="" border="0" /&gt;&lt;/a&gt;Since the 1950's Tetramethyl Ammonium Hydroxide has been used in the electrochemicals industries as a metal free base. More recently though, thanks to the work of Prof. Charles Little and others, strong organic bases such as TMAH and others have gain wide-spread acceptance in other fields of organic chemistry.&lt;br /&gt;&lt;br /&gt;The applications of TMAH and other related products such as Tetraethyl Ammonium Hydroxide and  Benzyltrimethyl Ammonium Hydroxide for use in pharmaceutical organic synthesis is also being examined very carefully.&lt;br /&gt;&lt;br /&gt;Sachem Inc. our partner for organic strong bases, have been producing these bases for over 50 years and thanks to their special processes can produce these materials with impurity profiles sometimes being measured at an incredible ppt level (yes, that's parts per trillion!).&lt;br /&gt;&lt;br /&gt;For more information please see this fascinating &lt;a href="http://www.d-orland.com/pdf/Strong_organic_bases.rtf" target="_blank"&gt;White Paper&lt;/a&gt; by Prof. Charles Little.&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/8830256984796565668-5527300629873215300?l=www.d-orland.com%2Fdefault.htm' alt='' /&gt;&lt;/div&gt;</content><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/5527300629873215300'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/5527300629873215300'/><link rel='alternate' type='text/html' href='http://www.d-orland.com/2007/03/high-purity-organic-bases.html' title='High Purity Organic Bases'/><author><name>robin</name><uri>http://www.blogger.com/profile/08864172896575683100</uri><email>noreply@blogger.com</email><gd:extendedProperty xmlns:gd='http://schemas.google.com/g/2005' name='OpenSocialUserId' value='14288062110727409832'/></author></entry><entry><id>tag:blogger.com,1999:blog-8830256984796565668.post-3767126963375545323</id><published>2007-02-26T17:58:00.000+01:00</published><updated>2007-03-31T14:11:09.434+01:00</updated><title type='text'>Methyl Tetrahydrofuran (MeTHF)</title><content type='html'>&lt;a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://www.pschem.com/images/midimage_agr.jpg"&gt;&lt;img style="margin: 10pt 10px 10px 10pt; float: right; cursor: pointer; width: 200px;" src="http://www.pschem.com/images/midimage_agr.jpg" alt="" border="0" /&gt;&lt;/a&gt;Methyl Tetrahydrofuran has often been over-looked as purely an over-expensive grignard solvent, with no real benefits over regular THF - except for it's higher boiling point. But this is to overlook the very clean phase splits and recycleability of the product - not to mention the fact that it is produced from corn husks - a renewal source. All this goes to make MeTHF a very ecologically sound choice. Read more in the downloadable pdf from Penn:&lt;br /&gt;&lt;br /&gt;&lt;ul&gt;&lt;li&gt;&lt;a href="http://www.d-orland.com/pdf/Methf.pdf" target="_blank"&gt;MeTHF for Greener Processes&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;Alternatively find out more from an &lt;a href="http://www.qdinformation.com/qdisblog/2006/07/26/methf-as-an-alternative-to-thf/"&gt;independent source&lt;/a&gt;&lt;br /&gt;&lt;ul&gt;&lt;span&gt;&lt;a href="http://www.qdinformation.com/qdisblog/2006/07/26/methf-as-an-alternative-to-thf/"&gt;&lt;/a&gt;&lt;/span&gt;&lt;/ul&gt;&lt;div class="blogger-post-footer"&gt;&lt;img width='1' height='1' src='https://blogger.googleusercontent.com/tracker/8830256984796565668-3767126963375545323?l=www.d-orland.com%2Fdefault.htm' alt='' /&gt;&lt;/div&gt;</content><link rel='edit' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/3767126963375545323'/><link rel='self' type='application/atom+xml' href='http://www.blogger.com/feeds/8830256984796565668/posts/default/3767126963375545323'/><link rel='alternate' type='text/html' href='http://www.d-orland.com/2007/02/methyl-tetrahydrofuran-methf.html' title='Methyl Tetrahydrofuran (MeTHF)'/><author><name>robin</name><uri>http://www.blogger.com/profile/08864172896575683100</uri><email>noreply@blogger.com</email><gd:extendedProperty xmlns:gd='http://schemas.google.com/g/2005' name='OpenSocialUserId' value='14288062110727409832'/></author></entry></feed>
