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Angewandte Chemie (International ed.), ISSN 1433-7851, 04/2014, Volume 53, Issue 18, pp. 4657 - 4661
A general method for the synthesis of α‐substituted vinyl sulfones makes use of a combination of a triazole gold complex and gallium triflate. This efficient C... 
gold | Lewis acids | CS bond formation | Markovnikov addition | vinyl sulfones | C-S bond formation
Journal Article
Advanced synthesis & catalysis, ISSN 1615-4150, 06/2015, Volume 357, Issue 9, pp. 2050 - 2054
Visible light and eosin Y catalyze the synthesis of vinyl sulfones from aryl sulfinates and alkenes by a photoredox process... 
metal‐free conditions | visible light | aryl sulfinates | photocatalysis | vinyl sulfones | metal-free conditions | Organosulfur compounds | Catalysis | Synthesis | Alkenes | Aromatic compounds | Sulfones
Journal Article
Chemistry : a European journal, ISSN 1521-3765, 07/2019, Volume 25, Issue 48, pp. 11193 - 11213
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 04/2014, Volume 53, Issue 16, pp. 4205 - 4208
Sulfone derivatives are important synthetic intermediates. However, the general method for their preparation is through traditional coupling reaction... 
CH activation | copper | sulfone derivatives | cleavage reactions | C-H activation | Copper | Acetates | Sodium | Derivatives | Oximes | Oxidants | Oxidizing agents | Joining | Bonding | Sulfones
Journal Article
Tetrahedron letters, ISSN 0040-4039, 05/2020, Volume 61, Issue 22, p. 151898
[Display omitted] •Photocatalyst-free visible light driven reactions.•(E)-vinyl sulfones from cinnamic acids and arylazo sulfones... 
Vinyl sulfones | Photocatalyst-free | Cinnamic acids | Arylazo sulfones
Journal Article
Chemical communications (Cambridge, England), ISSN 1359-7345, 2007, Issue 30, pp. 3123 - 3135
Over the last decade the potential of organocatalysis has successfully been demonstrated. In particular, chiral amines such as pyrrolidine analogues have... 
Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Amines - chemistry | Alkenes - chemistry | Vinyl Compounds - chemistry | Pyrrolidines - chemical synthesis | Stereoisomerism | Sulfones - chemistry | Nitro Compounds - chemistry | Catalysis | Pyrrolidines - chemistry | Index Medicus
Journal Article
Advanced synthesis & catalysis, ISSN 1615-4150, 06/2014, Volume 356, Issue 9, pp. 2029 - 2039
A highly efficient and mild palladium‐catalyzed cross‐coupling of sodium sulfinates and alkynes for the selective synthesis of unsymmetrical internal alkynes and vinyl sulfones has been developed... 
palladium catalyst | cross‐coupling | alkynes | sodium sulfinates | vinyl sulfones | cross-coupling | Palladium catalysts | Palladium | Organosulfur compounds | Synthesis | Sodium | Accessibility | Tolerances | Catalysis | Sulfones | Functional groups | Alkynes
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 06/2005, Volume 127, Issue 25, pp. 8948 - 8949
In this communication, we describe the development of the first highly enantioselective catalytic conjugate addition to vinyl sulfones... 
Vinyl Compounds - chemical synthesis | Vinyl Compounds - chemistry | Stereoisomerism | Sulfones - chemistry | Molecular Structure | Catalysis | Carbon - chemistry | Sulfones - chemical synthesis | Synthesis | Analysis | Amino acids | Chemical properties | Structure | Sulfones | Organic compounds | Index Medicus
Journal Article
Advanced synthesis & catalysis, ISSN 1615-4150, 11/2020, Volume 362, Issue 21, pp. 4744 - 4748
...)‐vinyl sulfones in moderate to good yields with excellent functional group tolerance. Preliminary mechanistic studies show that a vinyl radical‐induced 1,5... 
vinyl radical | sulfur dioxide insertion | 1,5-hydrogen atom transfer | metal-free | vinyl sulfones | Physical Sciences | Chemistry | Chemistry, Organic | Chemistry, Applied | Science & Technology | Sodium metabisulfite | Vinyl radical | Functional groups | Sulfones | Room temperature | Sulfur dioxide | Alcohols
Journal Article