A convenient and stereoselective synthesis of allylic sulfides
β Scribed by Kazunobu Harano; Norihide Ohizumi; Takuzo Hisano
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- French
- Weight
- 211 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
The fractional distillation of 0-(2-alkenyl or 2-cycloalkenyl) S-alkyl dithiocarbonates (xanthates) affords 2-alkenyl or 2-cycloalkenyl alk'yl
π SIMILAR VOLUMES
Trifluoromethyl aryl sulfides are obtained in moderate/good yields by heating potassium trifluoroacetate and aryl disulfides in sulfolane Copyright Β© 1996 Elsevier Science Ltd Trifluoromethyl aryl sulfides are important intermediates in the preparation of biologically active compounds, l dyes, 2 an
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
A mild chemo-, regio-, and diastereoselective substitution of ally1 carbonates and vinyl epoxides by sulfur nucleophiles catalyzed by palladium can overcome difficulties in and complement conventional displacement without poisoning of the catalyst.