Skeletal Migrations Observed during the Cob(I)alamin-Catalyzed Reduction of 4β-(tert-Butyl)-1β-(1-methylvinyl)cyclohexanecarbaldehyde
During the cob(I)alamin(1(I))‐catalyzed reduction of 3, intermediate formation of 2 and final generation of 4–10 was observed (see Scheme 1, cf. Tables 1 and 2). Identical products in similar ratios were generated starting from either 2 or 3. Accepting the intermediate formation of six interconnecte...
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Veröffentlicht in: | Helvetica chimica acta 1985-02, Vol.68 (1), p.181-184 |
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description | During the cob(I)alamin(1(I))‐catalyzed reduction of 3, intermediate formation of 2 and final generation of 4–10 was observed (see Scheme 1, cf. Tables 1 and 2). Identical products in similar ratios were generated starting from either 2 or 3. Accepting the intermediate formation of six interconnected cobalt complexes, i.e. A–F (cf. Scheme 2), the generation of all the products observed can be explained. |
doi_str_mv | 10.1002/hlca.19850680122 |
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Tables 1 and 2). Identical products in similar ratios were generated starting from either 2 or 3. Accepting the intermediate formation of six interconnected cobalt complexes, i.e. A–F (cf. Scheme 2), the generation of all the products observed can be explained.</description><identifier>ISSN: 0018-019X</identifier><identifier>EISSN: 1522-2675</identifier><identifier>DOI: 10.1002/hlca.19850680122</identifier><identifier>CODEN: HCACAV</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag GmbH</publisher><subject>Alicyclic compounds ; Alicyclic compounds, terpenoids, prostaglandins, steroids ; Chemistry ; Exact sciences and technology ; Organic chemistry ; Preparations and properties</subject><ispartof>Helvetica chimica acta, 1985-02, Vol.68 (1), p.181-184</ispartof><rights>Copyright © 1985 Verlag GmbH & Co. KGaA, Weinheim</rights><rights>1985 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2792-243695c148d6ac6ad35b9b985b3c5906bfea97539e8b6f77abbabcea15b7e10e3</citedby><cites>FETCH-LOGICAL-c2792-243695c148d6ac6ad35b9b985b3c5906bfea97539e8b6f77abbabcea15b7e10e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fhlca.19850680122$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fhlca.19850680122$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27915,27916,45565,45566</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=9072076$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Ziegler Jr, Carl B.</creatorcontrib><creatorcontrib>Fischli, Albert</creatorcontrib><title>Skeletal Migrations Observed during the Cob(I)alamin-Catalyzed Reduction of 4β-(tert-Butyl)-1β-(1-methylvinyl)cyclohexanecarbaldehyde</title><title>Helvetica chimica acta</title><addtitle>HCA</addtitle><description>During the cob(I)alamin(1(I))‐catalyzed reduction of 3, intermediate formation of 2 and final generation of 4–10 was observed (see Scheme 1, cf. Tables 1 and 2). Identical products in similar ratios were generated starting from either 2 or 3. Accepting the intermediate formation of six interconnected cobalt complexes, i.e. A–F (cf. Scheme 2), the generation of all the products observed can be explained.</description><subject>Alicyclic compounds</subject><subject>Alicyclic compounds, terpenoids, prostaglandins, steroids</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>Organic chemistry</subject><subject>Preparations and properties</subject><issn>0018-019X</issn><issn>1522-2675</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><recordid>eNqFkMFu1DAURS0EEkNhzzILFu3CxU7GdrxgUaLSVp20EgWB2FjPzktj6kkqO1MafoD_4UP4JjIaVMGK1ZOu7rlP9xLykrNDzlj-ugsODrkuBZMl43n-iCy4yHOaSyUekwVjvKSM689PybOUvjLGtGZqQX5c3WDAEUJW--sIox_6lF3ahPEOm6zZRN9fZ2OHWTXY_bMDCLD2Pa1gJqbvs-M9Nhu3pbKhzZa_ftL9EeNI327GKRxQvhU4XePYTeHO97PmJheGDu-hRwfRQmiwmxp8Tp60EBK--HP3yMd3xx-qU7q6PDmrjlbU5UrPbZaF1MLxZdlIcBKaQlht59a2cEIzaVsErUShsbSyVQqsBesQuLAKOcNij7BdrotDShFbcxv9GuJkODPbIc12SPPXkDPyaofcQnIQ2gi98-mBm2fMmZKz7c3O9s0HnP4ba05X1dG_b-iO92nE-wce4o2RqlDCfLo4MV_qi_r8qj43dfEb0zqYzA</recordid><startdate>19850213</startdate><enddate>19850213</enddate><creator>Ziegler Jr, Carl B.</creator><creator>Fischli, Albert</creator><general>WILEY-VCH Verlag GmbH</general><general>WILEY‐VCH Verlag GmbH</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19850213</creationdate><title>Skeletal Migrations Observed during the Cob(I)alamin-Catalyzed Reduction of 4β-(tert-Butyl)-1β-(1-methylvinyl)cyclohexanecarbaldehyde</title><author>Ziegler Jr, Carl B. ; Fischli, Albert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2792-243695c148d6ac6ad35b9b985b3c5906bfea97539e8b6f77abbabcea15b7e10e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Alicyclic compounds</topic><topic>Alicyclic compounds, terpenoids, prostaglandins, steroids</topic><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>Organic chemistry</topic><topic>Preparations and properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ziegler Jr, Carl B.</creatorcontrib><creatorcontrib>Fischli, Albert</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Helvetica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ziegler Jr, Carl B.</au><au>Fischli, Albert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Skeletal Migrations Observed during the Cob(I)alamin-Catalyzed Reduction of 4β-(tert-Butyl)-1β-(1-methylvinyl)cyclohexanecarbaldehyde</atitle><jtitle>Helvetica chimica acta</jtitle><addtitle>HCA</addtitle><date>1985-02-13</date><risdate>1985</risdate><volume>68</volume><issue>1</issue><spage>181</spage><epage>184</epage><pages>181-184</pages><issn>0018-019X</issn><eissn>1522-2675</eissn><coden>HCACAV</coden><abstract>During the cob(I)alamin(1(I))‐catalyzed reduction of 3, intermediate formation of 2 and final generation of 4–10 was observed (see Scheme 1, cf. Tables 1 and 2). Identical products in similar ratios were generated starting from either 2 or 3. Accepting the intermediate formation of six interconnected cobalt complexes, i.e. A–F (cf. Scheme 2), the generation of all the products observed can be explained.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag GmbH</pub><doi>10.1002/hlca.19850680122</doi><tpages>4</tpages></addata></record> |
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subjects | Alicyclic compounds Alicyclic compounds, terpenoids, prostaglandins, steroids Chemistry Exact sciences and technology Organic chemistry Preparations and properties |
title | Skeletal Migrations Observed during the Cob(I)alamin-Catalyzed Reduction of 4β-(tert-Butyl)-1β-(1-methylvinyl)cyclohexanecarbaldehyde |
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