Stereoselective synthesis of the C16–C25 fragment of alchivemycins A and B
Author:
Funder
National Natural Science Foundation of China
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Alchivemycin A, a Bioactive Polycyclic Polyketide with an Unprecedented Skeleton from Streptomyces sp.
2. Biosynthetic Origin of Alchivemycin A, a New Polyketide from Streptomyces and Absolute Configuration of Alchivemycin B
3. Studies towards the synthesis of the functionalized C3–C14 decalin framework of alchivemycin A
4. Access to the 2H-Tetrahydro-4,6-dioxo-1,2-oxazine Ring System from Nitrone via a Tandem Nucleophilic Addition and Transesterification Reaction
5. Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates
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. Total synthesis of alchivemycin A using a chemoenzymatic strategy;Nature Synthesis;2024-06-27
2. Chemoenzymatic total synthesis of alchivemycin A;Nature Synthesis;2024-06-25
3. Sharpless Asymmetric Dihydroxylation: An Impressive Gadget for the Synthesis of Natural Products: A Review;Molecules;2023-03-17
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