Asymmetric Total Synthesis and Structure Revision of (+)-Mangicol D

-mediated reductive cyclization to establish the spiro-fused tetracyclic framework in a concise manner. Our findings suggest a stereochemical revision of the polyol side chain of the initially isolated mangicols.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-04-02
DOI
https://doi.org/10.1021/jacs.6c01185
Primary Topic
Natural Compound Pharmacology Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Asymmetric Total Synthesis and Structure Revision of (+)-Mangicol D

Zhouyang Zhu, Thomas J. Maimone, Shang Ning, Yutong Wang et al.
Journal of the American Chemical Society
Natural Compound Pharmacology Studies
article

Asymmetric Total Synthesis and Structure Revision of (+)-Mangicol D

Zhouyang Zhu, Thomas J. Maimone, Shang Ning, Yutong Wang, Yi Xie
article en

Abstract

-mediated reductive cyclization to establish the spiro-fused tetracyclic framework in a concise manner. Our findings suggest a stereochemical revision of the polyol side chain of the initially isolated mangicols.

Journal of the American Chemical SocietyVol. 148(14)
University of California, Berkeley (US)
National Institutes of Health
Life below water
Openalex Percentile: Top 27%
Natural Compound Pharmacology Studies
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Asymmetric Total Synthesis and Structure Revision of (+)-Mangicol D — Zhouyang Zhu, Thomas J. Maimone, et al. · Journal of the American Chemical Society (2026) | TGRS Research Map | TGRS