α,α-Disubstituted Boron Enolates in the Asymmetric Synthesis of Quaternary Carbon Centers
Author:
Affiliation:
1. Department of Chemistry, McGill University, 801 Sherbrooke St. West, Montreal, Quebec, Canada, H3A 2K6
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol0364428
Reference12 articles.
1. Novel Isomerically Pure Tetrasubstituted Allylboronates: Stereocontrolled Synthesis of α-Exomethylene γ-Lactones as Aldol-Like Adducts with a Stereogenic Quaternary Carbon Center
2. Stereoselective Generation of E- and Z-Disubstituted Amide Enolates. Reductive Enolate Formation from Bicyclic Thioglycolate Lactams
3. Stereoselective Formation of Quaternary Carbon Centers: Alkylation ofα,α-Disubstituted Amide Enolates
4. New isoxazolidine-based chiral auxiliaries for asymmetric syntheses
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