N-Heterocyclic Carbene-Catalyzed Formal Intramolecular [3 + 2] Annulations of Cyclohexadienone-Tethered Ynals-Reference-Cited by-同舟云学术

N-Heterocyclic Carbene-Catalyzed Formal Intramolecular [3 + 2] Annulations of Cyclohexadienone-Tethered Ynals

Published:2024-04-19 Issue:17 Volume:26 Page:3552-3556
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Ya-Jie¹,Kang Wen-Yu¹,Zhao Yi-Wen¹,Wang Yu-Hui¹^ORCID,Tian Ping¹^ORCID

Affiliation:

1. The Research Center of Chiral Drugs, Innovation Research Institute of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, 1200 Cailun Road, Shanghai 201203, China

Funder

National Key Research and Development Program of China

State Administration of Traditional Chinese Medicine of the People's Republic of China

Shanghai University of Traditional Chinese Medicine

Science and Technology Commission of Shanghai Municipality

National Natural Science Foundation of China

Shanghai Frontiers Science Center for Traditional Chinese Medicine Chemical Biology

Shanghai Municipal Administration of Traditional Chinese Medicine, Shanghai Municipal Health Commission

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c00950

Reference38 articles.

1. Four‐Step Synthesis of (−)‐4‐ epi ‐Presilphiperfolan‐8 α ‐ol by Intramolecular Iron Hydride Atom Transfer‐Mediated Ketone‐Alkene Coupling and Studies to Access trans ‐Hydrindanols with a Botryane Scaffold

2. Synthetic Studies to exo‐Ring‐Junction based Fused 5/5/n‐Tricyclic Systems: Access to A, B, C‐Ring System of Longeracinphyllin A, Himalenine D, and Daphnipaxiamine A.

3. Tricyclic Sesquiterpenes from Marine Origin

4. Nine New Sesquiterpenes fromDendrobium nobile

5. Design and Synthesis of Highly Potent HIV-1 Protease Inhibitors Containing Tricyclic Fused Ring Systems as Novel P2 Ligands: Structure–Activity Studies, Biological and X-ray Structural Analysis

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