Sulfoxonium ylides: simple compounds with chameleonic reactivity
- 1 October 2020
- journal article
- review article
- Published by Royal Society of Chemistry (RSC) in Organic & Biomolecular Chemistry
- Vol. 18 (43) , 8793-8809
Abstract
Sulfoxonium ylides, manageable compounds with an appealing safety profile, adapt to reaction partners like chameleons to their environment, resulting in a variety of useful, and sometimes surprising and unique, reactions.Keywords
Funding Information
- Ministero dell’Istruzione, dell’Università e della Ricerca
- Università di Bologna
This publication has 109 references indexed in Scilit:
- Enantioselective cyclopropanation of enals by oxidative N-heterocyclic carbene catalysisChemical Communications, 2012
- Enantioselective Synthesis of Dihydropyrazoles by Formal [4+1] Cycloaddition of in Situ-Derived Azoalkenes and Sulfur YlidesJournal of the American Chemical Society, 2012
- Enantioselective Synthesis of 2,2-Disubstituted Terminal Epoxides via Catalytic Asymmetric Corey-Chaykovsky Epoxidation of KetonesMolecules, 2012
- Application of donor/acceptor-carbenoids to the synthesis of natural productsChemical Society Reviews, 2009
- Iridium-Catalyzed X−H Insertions of Sulfoxonium YlidesOrganic Letters, 2009
- Catalytic Asymmetric Synthesis of 2,2-Disubstituted Terminal Epoxides via Dimethyloxosulfonium Methylide Addition to KetonesJournal of the American Chemical Society, 2008
- One-Carbon Chain Extension of Esters to α-Chloroketones: A Safer Route without DiazomethaneThe Journal of Organic Chemistry, 2004
- Methylsulfinyl Carbanion (CH3-SO-CH2-). Formation and Applications to Organic SynthesisJournal of the American Chemical Society, 1965
- Dimethylsulfonium Methylide, a Reagent for Selective Oxirane Synthesis from Aldehydes and KetonesJournal of the American Chemical Society, 1962
- The Chemistry of Ylids. VI. Dimethylsulfonium Fluorenylide—A Synthesis of Epoxides1Journal of the American Chemical Society, 1961