AMINOSULFENYLATION OF OLEFINS BY SULFENAMIDES IN THE PRESENCE OF SULFAMINIC ACID, NH3*SO3

DOI: 10.1007/BF00962469

Source and publish data:

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 2634 (1989)

Update date:2022-07-29

Topics:

Authors:

Zefirov, N. S.

Zyk, N. V.

Kutateladze, A. G.

Butina, E. K.

Vatsadze, S. Z.

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

Article abstract of DOI:10.1007/BF00962469

Full text of DOI:10.1007/BF00962469

Products guided by the article

Product name:2-phenylthio-1-phenylethylamine hydrochloride

Cas No:127502-89-0

R&D Labs maybe for 127502-89-0

CHENGDU CHENLV HERB CO.,LTD

Contact:+86-28-88523492

Address:714rooms of Time Square, Pujiang County
Zhejiang Hoshine Silicon Industry Co., Ltd.

Contact:86-573-89179966

Address:Zhapu Town, Pinghu City, Zhejiang, China
SYN Pharma Co., Ltd

Contact:86-21 60347964

Address:No.1304, West Meilong Road, Minhang District, Shanghai, China
Suzhou ATL Chemical Co.,ltd

Contact:+86-0512-69209969

Address:Room 317,Lushan Road,Suzhou New District,Jiangsu Province,China.
HUNAN CHEMAPI BIOLOGICAL TECHNOLOGY CO.,LTD.

Contact:+86-186-02659358

Address:1004, building 3, Wanke Jinsemaitianyuan, 498 Guitang Road, Yuhua District, Changsha City, Hunan Province, China

Relevant to this article

Total synthesis and absolute stereochemistry of (+)-batzellaside B and its C8-epimer, a new class of piperidine alkaloids from the sponge batzella sp.

Doi:10.1016/j.tetlet.2011.01.018
(2011)
Synthesis and structure-activity relationship of disubstituted benzamides as a novel class of antimalarial agents

Doi:10.1016/j.bmcl.2012.05.124
(2012)
Polyhedral Iridathiaborane Chemistry. Reactions of nido-6-SB9H11 and of (1-) with <5-C5Me5)Cl2>2> to give nido-8,7-Iridathiaundecaboranes. A Nuclear Magnetic Resonance and Structural Study

Doi:10.1039/DT9910002657
(1991)
Heterogeneous copper-catalyzed oxidative coupling of oxime acetates with sodium sulfinates: An efficient and practical synthesis of β-keto sulfones

Doi:10.1002/aoc.5001
(2019)
Synthesis of (6S,6aS,7R,10S,10aR)-6-(Indol-3-yl)-7,11,11-trimethyl-5,6,6a,7,8,9,10,10a-octahydro-7,10-methanoindeno<2,1-b>indole and its Enantiomer: Absolute Configuration of Active Yuehchukene

Doi:10.1039/P19910002955
(1991)
Antifungal activities of new coumarins

Doi:10.3390/molecules17055713
(2012)

Article Doi