Diastereoselective (3 + 3)-Annulations of Trisubstituted Michael Acceptors for Access to Polyfunctional Cyclohexanones-Reference-Cited by-同舟云学术

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Diastereoselective (3 + 3)-Annulations of Trisubstituted Michael Acceptors for Access to Polyfunctional Cyclohexanones

Published:2024-03-19 Issue:8 Volume:89 Page:5878-5882
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Kitzinger Katelyn M.¹^ORCID,Giordano Mitchell T.¹,de Jesús Cruz Pedro¹,Johnson Jeffrey S.¹^ORCID

Affiliation:

1. Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-3290, United States

Funder

National Center for Advancing Translational Sciences

Division of Graduate Education

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c00157

Reference19 articles.

1. Formal carbo [3+3] annulation and its application in organic synthesis

2. One-Pot Organocatalytic Domino Michael-Aldol and Intramolecular SN2 Reactions. Asymmetric Synthesis of Highly Functionalized Epoxycyclohexanone Derivatives

3. Asymmetric Organocatalytic Domino Michael/Aldol Reactions: Enantioselective Synthesis of Chiral Cycloheptanones, Tetrahydrochromenones, and Polyfunctionalized Bicyclo[3.2.1]octanes

4. Enantioselective Synthesis of Protected Nitrocyclohexitols with Five Stereocenters. Total Synthesis of (+)-Pancratistatin

5. Enantioselective Assembly of Substituted Dihydropyrones via Organocatalytic Reaction in Water Media

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