Unexpected catalytic sulfur extrusion in the reaction of triphenylmethanesulfenyl chloride with thiocarbonyls
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Über Triphenyl‐thiocarbinol
2. Reagents for organic synthesis. Tin-assisted sulfuration: a highly potent new method for the conversion of carbonyl units into their corresponding thiocarbonyl analogs
3. Sulfur Extrusion Reactions - Scope and Mechanistic Aspects
4. Displacement Reactions at the Sulfur Atom. I. An Interpretation of the Decomposition of Acidified Thiosulfate
5. S�urezersetzung von Natriumthiosulfat: Molekulare Zusammensetzung des ausfallenden Schwefels
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1. Rapid Formation of a Dense Sulfur Layer on Gold through Use of Triphenylmethane Sulfenyl Chloride as a Precursor;Langmuir;2012-11-26
2. The organic chemistry of diatomic sulfur;Journal of Sulfur Chemistry;2006-02
3. New Sulfenyl Chloride Chemistry: Synthesis, Reactions and Mechanisms Toward Carbon-Carbon Double Bonds;Sulfur reports;2003-10
4. Highly Sulfurated Heterocycles via Dithiiranes and Trithietanes as Key Intermediates;The Journal of Organic Chemistry;2002-07-03
5. Chemistry of dithiiranes, 1,2-dithietanes, and 1,2-dithietes;Advances in Heterocyclic Chemistry;2000
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