Abstract
Diallyl sulfides were obtained in 60-90% yields by reaction of various allyl alcohols (1.0 equiv) with hexamethyldisilathiane (≈0.55 equiv) in CH 2 Cl 2 at room temperature in the presence of BF 3 ·OEt 2 (0.8-1.1 equiv). © 1993.
- Title
- Direct synthesis of diallyl sulfides from allyl alcohols and hexamethyldisilathiane
- Creators - without role
- Shwu-Chen Tsay - Institute of Chemistry, Academia SinicaGregory L. Yep - Johns Hopkins UniversityBuh-Luen Chen - Johns Hopkins UniversityLung Ching Lin - Institute of Chemistry, Academia SinicaJih Ru Hwu - Institute of Chemistry, Academia Sinica
- Publication Details
- Tetrahedron, Vol.49(40), pp.8969-8976
- Identifiers
- 9957773330206774
- Academic Unit
- National Tsing Hua University
- Language
- English
- Resource Type
- Journal article