Inter- and Intramolecular Annulation Strategies to a Cyclopentanone Building Block Containing an All-Carbon Quaternary Stereogenic Center
Author:
Affiliation:
1. BioFocus, a Charles River Company, Chesterford Research Park, Saffron Walden, Essex, CB10 1XL, United Kingdom
2. CHDI Management/CHDI Foundation Inc., 6080 Center Drive, Suite 100, Los Angeles, California 90045, United States
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b00207
Reference20 articles.
1. The Catalytic Enantioselective Construction of Molecules with Quaternary Carbon Stereocenters
2. Asymmetric Catalysis Special Feature Part I: Catalytic asymmetric synthesis of all-carbon quaternary stereocenters
3. Cascade Reactions in Total Synthesis
4. On the Mechanism of the Copper-Catalyzed Enantioselective 1,4-Addition of Grignard Reagents to α,β-Unsaturated Carbonyl Compounds
5. Catalytic Enantioselective Construction of All-Carbon Quaternary Stereocenters
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1. A concise access to bridged [2,2,1] bicyclic lactones with a quaternary stereocenter via stereospecific hydroformylation;Nature Communications;2021-09-06
2. N ‐Heterocyclic Carbene Catalyzed [3+2] Cycloaddition of Enals with β,γ ‐Unsaturated α ‐Ketimino Esters for the Synthesis of Multisubstituted Cyclopentanone;Advanced Synthesis & Catalysis;2020-01-16
3. Enantioselective synthesis of a substituted cyclopentanone with all-carbon quaternary stereocenter;ARKIVOC;2017
4. Enantioselective Synthesis of Functionalized Quaternary Stereocenters;European Journal of Organic Chemistry;2015-08-17
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