Mechanistic aspects of the isomerization of Z-vinylic tellurides double bonds in the synthesis of potassium Z-vinyltrifluoroborate salts


Autoria(s): STEFANI, Helio A.; GUADAGNIN, Rafael C.; KEPPLER, Artur F.; BOTTESELLE, Giancarlo V.; COMASSETO, Joao V.; SUGANUMA, Carlos A.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

17/04/2012

17/04/2012

2008

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

http://dx.doi.org/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