Reaction of Methoxycarbonylhydrazones with Hydrogen Sulfide: A New and Facile Synthesis of Tetrasulfides

作者： Roberto Ballini

DOI: 10.1055/S-1982-29962

关键词:

摘要:

thieme-connect.com 本地加速

thieme-connect.de 本地加速

unicam.it 本地加速

thieme-connect.de 本地加速

sci-hub.se PDF 下载加速

参考文章(0)

来源期刊

© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Reaction of Methoxycarbonylhydrazones with Hydrogen Sulfide: A New and Facile Synthesis of Tetrasulfides

来源期刊

相似文章 7

Sulfur: Organic Polysulfanes

Sulfur: Organic Polysulfanes

First direct synthesis of 4,8-dialkylbenzo[1,2-d;4,5-d']bis[1,2,3]trithioles and 6,10-dialkyl[1,2,3]trithiolo[5,4-h]benzopentathiepins from 1,4-dialkyl-2,3,5,6-tetrabromobenzenes

Synthesis and reactions of new cyclic polysulfides. 6,10-Disubstituted[1,2,3]trithiolo[5,4-h]benzopentathiepins

Novel Formations of Unsymmetrical 1,2,5-Benzotrithiepins from Olefins and Benzopentathiepin in the Presence of Lewis Acid. Benzopentathiepin as a Novel 1,5-Dipole Synthon

The chemistry of organic polysulfanes R-Sn-R (n > 2)

A “waiting” carbon nitride radical anion: a charge storage material and key intermediate in direct C–H thiolation of methylarenes using elemental sulfur as the “S”-source

我的账户