De Novo Asymmetric Approach to Aspergillide‐C: Synthesis of 4‐epi‐seco‐Aspergillide‐C-Reference-Cited by-同舟云学术

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De Novo Asymmetric Approach to Aspergillide‐C: Synthesis of 4‐epi‐seco‐Aspergillide‐C

Published:2022-04-11 Issue:14 Volume:7 Page:
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Xing Yalan¹,O'Doherty George A.²

Affiliation:

1. Department of Chemistry William Paterson University Wayne New Jersey 07470 USA

2. Department of Chemistry and Chemical Biology Northeastern University 360 Huntington Avenue Boston 02115 USA

Funder

National Institutes of Health

National Science Foundation

American Chemical Society Petroleum Research Fund

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.202200266

Reference61 articles.

1. New Cytotoxic 14-Membered Macrolides from Marine-Derived Fungus Aspergillus ostianus

2. For a review of the syntheses of Aspergillide A/B/C see:

3. Total Synthesis of Aspergillides A, B, and C

4. For a synthesis of Aspergillide A/B see:

5. A Unified Total Synthesis of Aspergillides A and B

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Exploring a De Novo Route to Bradyrhizose: Synthesis and Isomeric Equilibrium of Bradyrhizose Diastereomers^≠;Chemistry – A European Journal;2024-05-03

2. The Alkyne Zipper Reaction: A Useful Tool in Synthetic Chemistry;Reactions;2022-12-30

3. De novo asymmetric Achmatowicz approach to oligosaccharide natural products;Chemical Communications;2022

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