Author:
Hashimoto Takuya,Wata Chisato
Abstract
AbstractOrganoiodine-catalyzed enantioselective intramolecular oxyaminations were realized by the use of benzyl N-(fluorosulfonyl)carbamate as the exogenous nitrogen source. The method allows access to enantioenriched lactones and oxazolines, starting from γ,δ- and δ,ε-unsaturated esters and N-allyl amides, respectively.
Funder
Japan Society for the Promotion of Science
Subject
Organic Chemistry,Catalysis
Cited by
5 articles.
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