Iterative Stereospecific Reagent-Controlled Homologation Using a Functionalized α-Chloroalkyllithium: Synthesis of Cyclic Targets Related to Epibatidine
Author:
Affiliation:
1. Department of Chemistry, Oregon State University, Corvallis, Oregon 97331-4003, United States
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol103170y
Reference43 articles.
1. Reagent-Controlled Asymmetric Homologation of Boronic Esters by Enantioenriched Main-Group Chiral Carbenoids
2. Iterative Stereospecific Reagent-Controlled Homologation of Pinacol Boronates by Enantioenriched α-Chloroalkyllithium Reagents
3. Lithiated Carbamates: Chiral Carbenoids for Iterative Homologation of Boranes and Boronic Esters
4. Enantiodivergent conversion of chiral secondary alcohols into tertiary alcohols
5. Full Chirality Transfer in the Conversion of Secondary Alcohols into Tertiary Boronic Esters and Alcohols Using Lithiation-Borylation Reactions
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