Cope Rearrangement of 1-Acyl-2-vinylcyclopropanes to Cyclohept-4-Enones-Reference-Cited by-同舟云学术

Cope Rearrangement of 1-Acyl-2-vinylcyclopropanes to Cyclohept-4-Enones

Published:2024-01-02 Issue:2 Volume:89 Page:1127-1139
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Wei Yinhe¹,Wang Gang¹,Zhang Zhiguo¹^ORCID,Li Mengjuan¹,Ma Nana¹^ORCID,Wu Hao¹,Zhang Guisheng¹

Affiliation:

1. Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, Henan Key Laboratory of Organic Functional Molecule and Drug Innovation, Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang 453007, China

Funder

Henan Key Laboratory of Organic Functional Molecules and Drug Innovation

National Natural Science Foundation of China

Higher Education Discipline Innovation Project

Excellent Youth Foundation of Henan Scientific Committe

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c02319

Reference80 articles.

1. A General Strategy for the Construction of Calyciphylline A‐Type Alkaloids: Divergent Total Syntheses of (−)‐Daphenylline and (−)‐Himalensine A

2. Total Synthesis of (−)‐4‐ epi ‐Englerin A

3. Unified Enantioselective, Convergent Synthetic Approach toward the Furanobutenolide-Derived Polycyclic Norcembranoid Diterpenes: Synthesis of a Series of Ineleganoloids by Oxidation-State Manipulation of the Carbocyclic Core

4. Stereoselective Total Synthesis of (±)-5-epi-Cyanthiwigin I via an Intramolecular Pauson–Khand Reaction as the Key Step

5. Enantioselective Total Synthesis of (−)-Pavidolide B

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