Mechanistic aspects of the isomerization of Z-vinylic tellurides double bonds in the synthesis of potassium Z-vinyltrifluoroborate salts
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
17/04/2012
17/04/2012
2008
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Resumo |
Through direct transmetalation reaction of Z-vinylic tellurides with nBuLi was observed the unexpected isomerization of double bonds leading to potassium E-vinyltrifluoroborates salts in low to moderate yields. Using EPR spin trapping experiments the radical species that promoted the stereoinversion of Z-vinylic organometallic species during the preparation of potassium vinyltrifluoroborate salts was identified. The experiments support the proposed mechanism, which is based on the homolytic cleavage of the TenBu bond. |
Identificador |
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY, v.4, 2008 1860-5397 http://producao.usp.br/handle/BDPI/14824 10.1186/1860-5397-4-9 |
Idioma(s) |
eng |
Publicador |
BEILSTEIN-INSTITUT |
Relação |
Beilstein Journal of Organic Chemistry |
Direitos |
openAccess Copyright BEILSTEIN-INSTITUT |
Palavras-Chave | #CROSS-COUPLING REACTIONS #HYDROTELLURATION #STEREOCHEMISTRY #ACETYLENES #CARBON #Chemistry, Organic |
Tipo |
article original article publishedVersion |