ArticleOrganic letters2012
Stereoselective synthesis of cis-2,5-disubstituted pyrrolidines via Wacker-type aerobic oxidative cyclization of alkenes with tert-butanesulfinamide nucleophiles.
Article in Organic letters, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
7 citing papers in PubMed.
- Review
- Applications ofRSC advances · 2020Review
- Oxidative Cyclization of Sulfamates onto Pendant Alkenes.Organic letters · 2020Article
- Diastereoselective C-H Bond Amination for Disubstituted Pyrrolidines.Angewandte Chemie (International ed. in English) · 2017Article
- Catalytic Asymmetric Synthesis of Chiral γ-Amino Ketones via Umpolung Reactions of Imines.Journal of the American Chemical Society · 2016Article
- The syn/anti-dichotomy in the palladium-catalyzed addition of nucleophiles to alkenes.Chemistry (Weinheim an der Bergstrasse, Germany) · 2015Article
- Mechanistic studies of Wacker-type amidocyclization of alkenes catalyzed by (IMes)Pd(TFA)2(H2O): kinetic and stereochemical implications of proton transfer.The Journal of organic chemistry · 2013Article
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
Palladium(II)-catalyzed aerobic oxidative cyclization of alkenes with tethered tert-butanesulfinamides furnishes enantiopure 2,5-disubstituted pyrrolidines, originating from readily available and easily diversified starting materials. These reactions are the first reported examples of metal-catalyzed addition of sulfinamide nucleophiles to alkenes.
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Registered trials
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