1,2-Metallate Rearrangement as a Toolbox for the Synthesis of Allylic Alcohols
Author:
Affiliation:
1. Institute of Organic Chemistry, Gottfried Wilhelm Leibniz Universität Hannover, 30167 Hannover, Germany
2. Centre of Biomolecular Drug Research (BMWZ), Gottfried Wilhelm Leibniz Universität Hannover, 30167 Hannover, Germany
Funder
Deutsche Forschungsgemeinschaft
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c01309
Reference45 articles.
1. Discodermolide: a new bioactive polyhydroxylated lactone from the marine sponge Discodermia dissoluta
2. Conformational Behavior and Absolute Stereostructure of Two Phytotoxic Nonenolides from the Fungus Phoma herbarum
3. Catalytic Asymmetric Synthesis of Allylic Alcohols and Derivatives and their Applications in Organic Synthesis
4. Grignard-type carbonyl addition of allyl halides by means of chromous salt. A chemospecific synthesis of homoallyl alcohols
5. Reactions of alkenylchromium reagents prepared from alkenyl trifluoromethanesulfonates (triflates) with chromium(II) chloride under nickel catalysis
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2. Stereoselective Synthesis of Allylic Alcohols via Substrate Control on Asymmetric Lithiation;Chemistry – A European Journal;2023-11-22
3. Stereoselective Construction of β-chiral Homoallyl Functionalities by Substrate- and Reagent-Controlled Iterative 1,2-Metallate Rearrangements;Organic Letters;2023-11-09
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