Conjugate addition of α-(trialkylstannyl)alkyl groups to α,β-enones: Preparation of γ-stannyl ketones

DOI: 10.1246/bcsj.66.3825

Source and publish data:

Bulletin of the Chemical Society of Japan p. 3825 - 3827 (1993)

Update date:2022-08-05

Topics:

Authors:

Sato Sato

Tachibana

Kawase Kawase

Hirose Hirose

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

Article abstract of DOI:10.1246/bcsj.66.3825

The title reaction was examined under various conditions. The corresponding cuprates underwent 1,4-addition satisfactorily to afford γ- stannyl ketones.

Full text of DOI:10.1246/bcsj.66.3825

Products guided by the article

Product name:(CH₂)3C(O)CH₂CHCH(Et)Sn(n-Bu)3

Cas No:146399-03-3

R&D Labs maybe for 146399-03-3

Zhengzhou Yuanli Biological Technology Co., Ltd.

Contact:+86-371-67897870/67897895

Address:No. 38, Qingyang Street, Zhengzhou, Henan, China
Nanjing Habo Medical Technology Co., Ltd.

Contact:025－85769882

Address:No.108. Ganjiabian east. Qixia District .Nanjing
ANGCHEN BRIGHTCHEM CO., LTD

website:http://www.angchenchem.com

Contact:+86-510-88302099 82327577

Address:Rm. 404/405, Floor 4th, No. 983 FengXiang Road, Wuxi, China
Tianjin Chemsyntech Chemical Co., Ltd

Contact:+86-22-60872258

Address:Haitai green industry base in Tianjin, K1,5-601
jintan yufan Medicine Raw materials Co.,Ltd.(expird)

Contact:86-519-82808282

Address:6th,Jincheng Huangzhuang

Relevant to this article

Site-Selective Acylations with Tailor-Made Catalysts

Doi:10.1002/chem.201600790
(2016)
Synthesis and structural analysis of Bis(2-hydroxyphenyl) phenylamine, PhN(o-C₆H₄OH)₂: Comparison with Tris(2-hydroxyphenyl)amine N(o-C₆H₄OH)₃

Doi:10.1007/s10870-005-5360-0
(2005)
Formation of 2-acetamido-2-deoxy-d-glucopyranosidic linkages via glycosidation using a combination of two lewis acids

Doi:10.3987/COM-14-S(K)4
(2015)
Doi:10.1021/ja00451a041
(1977)
Doi:10.1016/0040-4020(77)80078-1
(1977)
Doi:10.1021/jm00187a026
(1979)

Article Doi