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Diastereoselective Pyrrolidine Synthesis via Copper Promoted Intramolecular Aminooxygenation of Alkenes; Formal Synthesis of (+)-Monomorine

[Image: see text] The diastereoselectivity of the copper-promoted intramolecular aminooxygenation of various alkene substrates was investigated. α-Substituted 4-pentenyl sulfonamides favor the formation of 2,5-cis-pyrrolidines (dr >20:1) giving excellent yields which range from 76–97% while γ-sub...

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Detalhes bibliográficos
Main Authors: Paderes, Monissa C, Chemler, Sherry R
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2714983/
https://ncbi.nlm.nih.gov/pubmed/19331361
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol9003492
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