Syntheses of Ketene Thioselenoacetals and of γ-Unsaturated Se-Alkyl Carboxylic Thionoselenoesters

DOI: 10.1016/S0040-4039(00)60024-2

Source and publish data:

Tetrahedron Letters p. 6131 - 6134 (1992)

Update date:2022-08-03

Topics:

Authors:

Lemarie, Margareth

Vallee, Yannick

Worrell, Mark

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

Article abstract of DOI:10.1016/S0040-4039(00)60024-2

The alkylation of Se-alkyl carboxylic thionoselenoesters enethiolates stereoselectively leads to ketene thioselenoacetals.When the alkylation is conducted with an allylic halide a thio-Claisen rearrangement is observed.

Full text of DOI:10.1016/S0040-4039(00)60024-2

Products guided by the article

Product name:((E)-2-Allylsulfanyl-2-methylselanyl-vinyl)-benzene

Cas No:144937-54-2

R&D Labs maybe for 144937-54-2

Taizhou Chemedir Biopharm-tech Co., Ltd

Contact:+86 523 86200218

Address:G09, No. 1 Avenue China Medical City, Taizhou,Jiangsu, China
Beijing Apis Biotechnology Co., Ltd.

Contact:86-010-67856775-8551

Address:NO.4PUHUANGYU ROAD,FENTAI DISTRICT, BEIJING, CHINA
EAST CHEMSOURCES LIMITED

website:http://www.eastchem-cn.com

Contact:15053231572

Address:No.1581-12,Jinshui Road, Licang, Qingdao,China
Xian Changyue Biological Technology Co., Ltd.

website:https://www.xachangyue.com/

Contact:+86-029-88211911

Address:Keji Road NO.70
Hangzhou Sartort Biopharma Co., Ltd

website:http://www.sartort.com

Contact:86-571-87039693

Address:No. 57, Tech Park Road, Hangzhou, Zhejiang, China

Relevant to this article

Synthesis and properties of the 5,10,15-trimesityltruxen-5-yl radical

Doi:10.1021/ol402153w
(2013)
An Organocatalytic Two-atom Ring Expansion Approach to Optically Active Glutarimides

Doi:10.1002/adsc.201900159
(2019)
Ruthenium-amine electronic coupling bridged through phen-1,3-diyl versus phen-1,4-diyl: Reverse of the charge transfer direction

Doi:10.1021/om400519b
(2013)
Organocatalytic Asymmetric Synthesis of Chiral Dioxazinanes and Dioxazepanes with in Situ Generated Nitrones via a Tandem Reaction Pathway Using a Cooperative Cation Binding Catalyst

Doi:10.1021/jacs.6b10660
(2016)
Regioselective Access to Structurally Diverse Coumarin Analogues through Iron-Catalysed Annulation Reactions

Doi:10.1002/ejoc.201700999
(2017)
Homo-Diels-Alder reaction of a very inactive diene, bicyclo[2,2,1]hepta-2, 5-diene, with the most active dienophile, 4-phenyl-1,2,4-triazolin-3,5-dione. Solvent, temperature, and high pressure influence on the reaction rate

Doi:10.1002/poc.3054
(2013)

Article Doi