A convenient synthesis of episulfides and their conversion into alkenes

DOI: 10.1055/s-1997-1329

Source and publish data:

Synthesis p. 1134 - 1136 (1997)

Update date:2022-07-31

Topics:

Authors:

Dybowski, Piotr

Skowrońska, Aleksandra

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1055/s-1997-1329

A convenient and stereoselective synthesis of episulfides based on the reaction of readily available S-(β-oxoalkyl) thiophosphate with sodium borohydride and their conversion into alkenes is described.

Full text of DOI:10.1055/s-1997-1329

Products guided by the article

Product name:Thiirane, 2-(1-methylethyl)-3-(2-methylpropyl)-, cis- (9CI)

Cas No:199617-39-5

R&D Labs maybe for 199617-39-5

Sichuan Highlight Fine Chemicals Co., Ltd.

Contact:+86-28-8525 1605

Address:A5-102 Airport base,388 West Airport Huang He Zhong Lu,2 Section
xujianqiang

Contact:86-21-57725962

Address:shanghai
HEZE KINGVOLT CHEMICAL CO., LTD

Contact:86-573-82118911

Address:Juancheng Industry Park
Zouping Mingxing Chemical Co.,Ltd.

website:http://www.zoutong.com.cn

Contact:86-543-2240068 2240067

Address:428 Daixi Third Road Zouping County Shandong Province China
Hawks Chemical

Contact:+44 (0)161 367 9441

Address:

Relevant to this article

Synthesis of oxygenated hererecycles from cyclic allylsiloxanes using ring-closing olefin metathesis

Doi:10.1016/S0040-4039(97)10147-2
(1997)
Synthesis of a key intermediate for the synthesis of (+)-grandisol utilizing (-)-quinic acid

Doi:10.1248/cpb.45.1734
(1997)
Benzoxazin-4-ones as novel, easily accessible inhibitors for rhomboid proteases

Doi:10.1016/j.bmcl.2017.12.056
(2018)
Doi:10.1021/ja01009a027
(1968)
A New Route to Substituted Dihydropyrans

Doi:10.1055/s-1997-1017
(1997)
BOIMPYs: Rapid Access to a Family of Red-Emissive Fluorophores and NIR Dyes

Doi:10.1002/anie.201606883
(2016)

Article Doi