Application of Free Radical Substitution Reaction into Interconversion of 1-Alkenylsulfides, 1-Alkenylgermanes, and 1-Alkenylstannanes

DOI: 10.1246/cl.1988.669

Source and publish data:

Chemistry Letters p. 669 - 672 (1988)

Update date:2022-08-04

Topics:

Authors:

Ichinose, Yoshifumi

Oshima, Koichiro

Utimoto, Kiitiro

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

Article abstract of DOI:10.1246/cl.1988.669

Treatment of 1-alkenylsulfides or 1-alkenylstannanes with Ph3GeH in the presence of Et3B provides 1-alkenyltriphenylgermanes in good yields. 1-Alkenylstannanes are converted into 1-alkenylsulfides easily with PhSH-Et3B, whereas 1-alkenyltriphenylgermanes are recovered unchanged upon treatment with Ph3SnH-Et3B or PhSH-Et3B.

Full text of DOI:10.1246/cl.1988.669

Products guided by the article

Product name:(CH₂CH₂CH₂CH₂)CCH(Ge(C₆H₅)3)

Cas No:120677-78-3

R&D Labs maybe for 120677-78-3

Jiangxi Biochem Co.,Ltd

Contact:86-791-86629460

Address:1-6F, 118 Xinzhou road, Nanchang, Jiangxi, China
zhuzhou zhongle chemical co. ltd.

Contact:+86-0731 28228409

Address:Zhuzhou, Hunan, China
MedicalChem(Yancheng)Manuf.Co.,Ltd.

Contact:+86-515-84383366

Address:Touzeng BinHai, YanCheng City, JiangSu Province, China
Weifang Arylchem Chemical Co., LTD

Contact:86-536-5217866

Address:Development Zone, Shouguang, Shandong Province
DU-HOPE INTERNATIONAL GROUP

Contact:+86-25-52346955

Address:199,JIANYE ROAD,NANJING,CHINA

Relevant to this article

Reduction of cobalt and iron corroles and catalyzed reduction of CO₂

Doi:10.1021/jp013668o
(2002)
Comparative study between the anti-P. falciparum activity of triazolopyrimidine, pyrazolopyrimidine and quinoline derivatives and the identification of new PfDHODH inhibitors

Doi:10.1016/j.ejmech.2020.112941
(2021)
Convenient synthesis of disulfide substrates for trypanothione reductase using polymer-supported reagents

Doi:10.1016/S0040-4039(02)00064-3
(2002)
Fluoride ion abstraction of phosphonium cations from their counter anion: A novel synthetic method of fluorophosphoranes

Doi:10.1246/cl.2002.268
(2002)
Doi:10.1021/ja01873a501
(1939)
Effect of modification of 6-[(aminoalkyl)amino]-7H-benzo[e]-perimidin-7-ones on their cytotoxic activity toward sensitive and multidrug resistant tumor cell lines. Synthesis and biological evaluation

Doi:10.1016/S0968-0896(01)00358-3
(2002)

Article Doi