A one pot cobalt catalyzed regio- and stereoselective synthesis of oxazolidin-2-thiones from alkenes and trimethylsilylisothiocyanate
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Cysteine- and serine-derived thiazolidinethiones and oxazolidinethiones as efficient chiral auxiliaries in aldol condensations
2. Synthesis of the branched nine-carbon unit of the type A streptogramins and other antibiotics
3. A Novel Rearrangement of Oxazolidin-2-thione Chiral Auxiliaries in the Preparation of α-Alkyl-β-Hydroxy Esters
4. An Alternative Route to cis-1,2-Fused Oxazolidine-2-Thione from 1,2-O-Sulfinyl Sugar Derivatives
5. Chiral 2-thioxotetrahydro-1,3-O,N-heterocycles from carbohydrates
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1. Highly chemo- and regioselective synthesis and subsequent directional catalyst-free transformation of enantiopure bioxirane derivatives;Tetrahedron;2022-05
2. Transition‐Metal‐Catalyzed Aminooxygenation of Alkenes;Organic Reactions;2021-11-30
3. Reaction of (+)-Carvone with Several Hetarylsulfenyl Chlorides and Pyridylselenyl Chloride;Chemistry of Natural Compounds;2014-05
4. Regio- and stereoselective methods for the conversion of (2S,3R)-β-phenylglycidic acid esters to taxoids and other enantiopure (2R,3S)-phenylisoserine esters;Russian Chemical Bulletin;2012-11
5. ChemInform Abstract: A One-Pot Cobalt Catalyzed Regio- and Stereoselective Synthesis of Oxazolidin-2-thiones from Alkenes and Trimethylsilylisothiocyanate.;ChemInform;2010-08-04
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