Asymmetric Synthesis of Cyclopentene Compounds Containing All-Carbon Quaternary Stereocenters by (3 + 2) Cycloaddition and Its Application in the Formal Synthesis of (R)-(−)-Puraquinonic Acid
Author:
Affiliation:
1. Department of Applied Chemistry, Keio University, Hiyoshi, Kohoku-ku, Yokohama 223-8522, Japan
Funder
Japan Society for the Promotion of Science
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c00753
Reference44 articles.
1. The structure and chemistry of hirsutic acid
2. Sterhirsutins A and B, Two New Heterodimeric Sesquiterpenes with a New Skeleton from the Culture of Stereum hirsutum Collected in Tibet Plateau
3. Russulactarorufin, a lactarane skeleton sesquiterpene from Russula brevipes
4. Puraquinonic Acid, a Novel Inducer of Differentiation of Human HL-60 Promyelocytic Leukemia Cells fromMycena pura(Pers. Ex Fr.)
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1. Phosphine-Catalyzed [3+2] Annulation of Hepta-2,3,5-trienedioates with Alkenes for the Construction of Exocyclic Olefinic Cyclopentenes;The Journal of Organic Chemistry;2023-07-11
2. Sodiated Oppolzer enolates: solution structures, mechanism of alkylation, and origin of stereoselectivity;Organic Chemistry Frontiers;2023
3. Recent Progress on the [3+2] Cycloaddition Route for the Synthesis of All-Carbon Quaternary Stereocentres;SynOpen;2022-09-20
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