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Synlett 2014; 25(2): 163-169
DOI: 10.1055/s-0033-1340303
DOI: 10.1055/s-0033-1340303
synpacts
Catalytic Enantioselective Halocyclizations beyond Lactones: Emerging Routes to Enantioenriched Nitrogenous Heterocycles
Further Information
Publication History
Received: 21 September 2013
Accepted after revision: 21 October 2013
Publication Date:
03 December 2013 (online)
Abstract
Electrophilic halogen-induced reactions of unactivated olefins are an important class of transformations, whose catalytic enantioselective variants have surfaced during the past few years as effective means of olefin heterodifunctionalization. This article covers important developments in the area of enantioselective halocyclizations, specifically in the context of the synthesis of nitrogenous heterocycles.
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For recent reviews, see:
For halofunctionalization of α,β-unsaturated carbonyls, see refs. 4c, 4h and:
For reviews on anion-binding catalysis, see:
For a recent report on enantioselective carbosulfenylation, see:
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For the sole example of intermolecular halofunctionalization of unactivated olefins, see:
For some related transformations, see refs. 16a, 16f and: