Vinyl bis-sulfone methodology in thiosugars: selective access to chiral thiovinyl sulfones and PSE oxathianes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference32 articles.
1. Synthesis, Structural Analysis and Reactivity of 1,3-Oxathiane Derivatives
2. Asymmetric syntheses based on 1,3-oxathianes. 1. Scope of the reaction
3. Asymmetric syntheses based on 1,3-oxathianes. 2. Synthesis of chiral tertiary .alpha.-hydroxy aldehydes, .alpha.-hydroxy acids, glycols [R1R2C(OH)CH2OH], and carbinols [R1R2C(OH)Me] in high enantiomeric purity.
4. Asymmetric reactions based on 1,3-oxathianes3̄
5. New S,O-acetals from (1R)-(−)-myrtenal as chiral auxiliaries in nucleophilic additions
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2. Carbohydrate-derived PSE acetals: controlled base-induced ring cleavage;Tetrahedron;2012-01
3. Desulfonylation Reactions;Organic Reactions;2009-03-16
4. Diphenylphosphinoylethylidene (DPE) acetals: an alternative protective strategy in glycochemistry;Tetrahedron Letters;2009-01
5. 1,2-Glycerol Carbonate: A Versatile Renewable Synthon;Letters in Organic Chemistry;2006-10-01
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