Direct synthesis of diallyl sulfides from allyl alcohols and hexamethyldisilathiane

Autor:	Lung Ching Lin, Shwu-Chen Tsay, Gregory L. Yep, Jih Ru Hwu, Buh-Luen Chen
Rok vydání:	1993
Předmět:	Chemistry Organic Chemistry Drug Discovery Organic chemistry Lewis acids and bases Aliphatic compound Biochemistry Catalysis
Zdroj:	Tetrahedron. 49:8969-8976
ISSN:	0040-4020
Popis:	Diallyl sulfides were obtained in 60–90% yields by reaction of various allyl alcohols (1.0 equiv) with hexamethyldisilathiane (≈0.55 equiv) in CH2Cl2 at room temperature in the presence of BF3·OEt2 (0.8–1.1 equiv).
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::eb0c0944b6cd4ea300bd18e6bed9fa2d https://doi.org/10.1016/s0040-4020(01)91216-5 Zobrazit plný text záznamu