In situ generation of n-butanethiol and its reaction with electron-deficient olefines


Autoria(s): GARIANI, Rogerio A.; SANTOS, Alcindo A. Dos; COMASSETO, Joao V.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2008

Resumo

n-Butanethiol is generated in situ by sequential addition of n-butyllithium and water to elemental sulfur. The n-butanethiol formed was reacted with electron-deficient olefines to give Michael-type addition products in good yields. The method avoids the manipulation of the bad-smelling n-butanethiol.

Identificador

SYNTHETIC COMMUNICATIONS, v.38, n.5, p.789-795, 2008

0039-7911

http://producao.usp.br/handle/BDPI/31363

10.1080/00397910701820897

http://dx.doi.org/10.1080/00397910701820897

Idioma(s)

eng

Publicador

TAYLOR & FRANCIS INC

Relação

Synthetic Communications

Direitos

restrictedAccess

Copyright TAYLOR & FRANCIS INC

Palavras-Chave #Michael addition #thiols #alpha,beta-unsaturated carbonyl compound #MICHAEL ADDITION #CARBONYL-COMPOUNDS #IONIC LIQUID #THIOLS #ALKENES #HYDROTELLURATION #CATALYSIS #TELLURIUM #Chemistry, Organic
Tipo

article

original article

publishedVersion