Preparation of optically active stilbene oxides via sulfonium salts derived from C2 symmetric thiolanes

DOI: 10.1016/S0040-4039(00)94327-2

Source and publish data:

Tetrahedron Letters p. 35 - 38 (1990)

Update date:2022-09-26

Topics:

Authors:

Breau Breau

Ogilvie Ogilvie

Durst Durst

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

Article abstract of DOI:10.1016/S0040-4039(00)94327-2

Trans-stilbene oxides have been obtained in up to 83% enantiomeric excess via reaction of S-benzyl ylides prepared from optically active trans-2,5-disubstituted thiolanes.

Full text of DOI:10.1016/S0040-4039(00)94327-2

Products guided by the article

Product name:trans-4,4'-dinitrostilbeneoxide

Cas No:58966-18-0

R&D Labs maybe for 58966-18-0

Chengdu ZY Biochemical Technology Co., LTD

Contact:0086-28-88680086

Address:170 Qingpu Road, Shouan Town, Pujiang County
Shanghai doly chemical Co.,Ltd

Contact:+86-21-34716221

Address:No.328,WuHe Roard,MinHang,ShangHai China
Guangxi Shanyun Biochemical Science and Technology Co., Ltd

Contact:+86-0772--6828887

Address:#2 Industrial Park of Luzhai County, Liuzhou, Guangxi, China
JIANGXI XINXIN CHEMICAL CO., LTD.

Contact:86-15957176628

Address:INDUSTRY ROAD 1, INDUSTRIAL PARK, HEKOU TOWN,YANSHAN COUNTY, JIANGXI PROVINCE, CHINA
Wuhan Hanye Chemical New Material Co.,Ltd

Contact:+86-27-85308141

Address:LiuDian, Panlongcheng Economic Development Zone, HuangPi district, Wuhan, Hubei 430311 P.R.China

Relevant to this article

Synthesis of Alkynyl-Glycinols by Lewis Acid Catalyzed Propargylic Substitution of Bis-Imidates

Doi:10.1002/ejoc.201500937
(2015)
Intramolecular 1,5-H transfer reaction of aryl iodides through visible-light photoredox catalysis: A concise method for the synthesis of natural product scaffolds

Doi:10.1039/c6cc02007k
(2016)
Doi:10.1055/s-1975-23928
(1975)
Heteronoradamantanes Me₂Si₂ (RM)₂E₅ (RM=MeGe, PhSn; E=S, Se)

Doi:10.1016/S0022-328X(03)00226-2
(2003)
Doi:10.1016/S0008-6215(00)84285-8
(1975)
Theory and example of a small-molecule motor

Doi:10.1002/poc.591
(2003)

Article Doi