Dialkylzinc Additions to 4-Acetoxy-1,3-dioxanes: A Highly Stereoselective Route to Protected anti-1,3-Diols
Author:
Affiliation:
1. Department of Chemistry, University of California, Irvine, California 92697-2025
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo971207m
Reference22 articles.
1. Preparation and reactions of polyfunctional organozinc reagents in organic synthesis
2. Preparation of functionalized dialkylzinc reagents via an iodine-zinc exchange reaction. Highly enantioselective synthesis of functionalized secondary alcohols
3. Preparation and reaction of new dialkylzincs obtained by a boron-zinc transmetalation.
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1. Synthesis of chiral propargyl alcohols following the base-induced elimination protocol: application in the total synthesis of natural products;New Journal of Chemistry;2020
2. Organozinc reagents;Fieser and Fieser's Reagents for Organic Synthesis;2017-02-21
3. Organozinc reagents;Fieser and Fieser's Reagents for Organic Synthesis;2017-02-21
4. Versatile process for the stereodiverse construction of 1,3-polyols: iterative chain elongation with chiral building blocks;Chemical Communications;2016
5. A Chiral Building Block for the Stereocontrolled Installation of the 1,3-Diol Motif;European Journal of Organic Chemistry;2015-11-24
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