Cyclization of 1,3-diaryl-3-phenylsulfanyl-1-propanols to thiochromans with the participation of [1,3]-PhS shift
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Recent Advances in Catalytic Enantioselective Michael Additions
2. Simple preparation of enantiomeric Michael adducts of thiophenol to chalcones: easily available new chiral building blocks
3. A new and efficient route to homochiral γ-hydroxysulfoxides and γ-hydroxysulfones
4. Preparation of thiochromansviathermal cyclization
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1. Triflic-Acid-Catalyzed Tandem Allylic Substitution–Cyclization Reaction of Alcohols with Thiophenols—Facile Access to Polysubstituted Thiochromans;ACS Omega;2018-08-10
2. 4.1.3.3. Organocatalytic Enantioselective Michael Addition of Thiophenol to Chalcone;Comprehensive Organic Chemistry Experiments for the Laboratory Classroom;2016-12-16
3. Two expedient ‘one-pot’ methods for synthesis of β-aryl-β-mercaptoketones over anhydrous potassium carbonate or amberlyst-15 catalyst;Journal of Chemical Sciences;2013-11
4. Facile Diastereoselective Synthesis of Carbohydrate-Based Thiochromans;Journal of Carbohydrate Chemistry;2013-02-12
5. A facile and highly diastereoselective synthesis of cis-2,4-diarylthiochromans;Arkivoc;2012-09-29
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