Cyclization Reaction of Bis(tributylstannylated) α-Ketols with Heterocumulenes. Preparation of O,O-Vinylene Imino- and Thiocarbonates

DOI: 10.1246/bcsj.56.1873

Source and publish data:

Bulletin of the Chemical Society of Japan p. 1873 - 1874 (1983)

Update date:2022-08-03

Topics:

Authors:

Sakai, Shizuyoshi

Murata, Masashi

Wada, Nobuto

Fujinami, Tatsuo

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

Article abstract of DOI:10.1246/bcsj.56.1873

Aromatic α-ketols reacted with diethylaminotributylstannane at 60 deg C to afford a mixture of (Z)- and (E)-1,2-bis(tributylstannyloxy)-1,2-diarylethenes, which were allowed to react with organic isothiocyanates and carbon disulfide to give substituted O,

Full text of DOI:10.1246/bcsj.56.1873

Products guided by the article

Product name:C₆H₅COCH(C₆H₅)OSn(C₄H₉)3

Cas No:86859-96-3

R&D Labs maybe for 86859-96-3

Shanghai doly chemical Co.,Ltd

Contact:+86-21-34716221

Address:No.328,WuHe Roard,MinHang,ShangHai China
Foreschem Co., Ltd

Contact:+86-533-3112891

Address:zibo
wuxi leji biology technology co., LTD

website:http://www.lejibio.com/

Contact:18362718864

Address:The Nanyue Road No. 2, Yixing City, Jiangsu Province
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
Hangzhou Neway Chemicals Co., Ltd.

Contact:+86-571-85095566

Address:Room 803, Qinglian Bldg, No 139 Qingchun Road, Hangzhou, Zhejiang China

Relevant to this article

HEMIACETALIC THAPSANE DERIVATIVES FROM THAPSIA VILLOSA VAR. MINOR

Doi:10.1016/0031-9422(86)88028-1
(1986)
Doi:10.1021/ja00224a025
(1988)
p-(dimethylamino)benzaldehyde modification of the Hantzsch reaction: Synthesis of 3-(1H-benzimidazol-2-yl)-5,7-dimethoxyquinolines

Doi:10.1007/s10593-007-0235-2
(2007)
Diastereo- and enantioselective addition of anilide-functionalized allenoates to N-acylimines catalyzed by a pyridylalanine-based peptide

Doi:10.1021/ja412996f
(2014)
1,3,4-Oxadiazol-2-ylbenzenesulfonamides as privileged structures for the inhibition of monoamine oxidase B

Doi:10.1016/j.bmcl.2019.126677
(2019)
Doi:10.1246/bcsj.34.1382
(1961)

Article Doi