Enantioselective Total Synthesis of (+)-Peniciketals A and B: Two Architecturally Complex Spiroketals-Reference-Cited by-同舟云学术

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Enantioselective Total Synthesis of (+)-Peniciketals A and B: Two Architecturally Complex Spiroketals

Published:2021-01-26 Issue:4 Volume:143 Page:1740-1744
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Deng Yifan¹,Yang Chia-Ping H.²,Smith III Amos B.¹^ORCID

Affiliation:

1. Department of Chemistry, University of Pennsylvania, 231 S. 34th Street, Philadelphia, Pennsylvania 19104, United States

2. Department of Molecular Pharmacology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, New York 10461, United States

Funder

Foundation for the National Institutes of Health

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.0c11424

Reference21 articles.

1. Peniciketals A–C, New Spiroketals from Saline Soil Derived Penicillium raistrichii

2. Peniciketal A, A Novel Spiroketal Compound, Exerts Anticancer Effects by Inhibiting Cell Proliferation, Migration and Invasion of A549 Lung Cancer Cells

3. Effects of a spiroketal compound Peniciketal A and its molecular mechanisms on growth inhibition in human leukemia

4. Analysis of Comparative Proteomic and Potent Targets of Peniciketal A in Human Acute Monocytic Leukemia

5. Benzannulated spiroketal natural products: isolation, biological activity, biosynthesis, and total synthesis

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