Total synthesis of nitropyrrolins A, B, and D-Reference-Cited by-同舟云学术

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Total synthesis of nitropyrrolins A, B, and D

Published:2016-11 Issue:45 Volume:72 Page:7179-7184
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Mitani Hikaru,Matsuo Tomoki,Kodama Takeshi,Nishikawa Keisuke,Tachi Yoshimitsu,Morimoto Yoshiki

Funder

Japan Society for the Promotion of Science

Asahi Glass Foundation

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. Nitropyrrolins A−E, Cytotoxic Farnesyl-α-nitropyrroles from a Marine-Derived Bacterium within the Actinomycete Family Streptomycetaceae

2. Heronapyrroles A−C: Farnesylated 2-Nitropyrroles from an Australian Marine-Derived Streptomyces sp.

3. Heronapyrrole D: A case of co-inspiration of natural product biosynthesis, total synthesis and biodiscovery

4. High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids

5. Biomimetic Synthesis and Proposal of Relative and Absolute Stereochemistry of Heronapyrrole C

Cited by 6 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. Marine Pyrrole Alkaloids;Marine Drugs;2021-09-10

2. Cross-coupling reactions towards the synthesis of natural products;Molecular Diversity;2021-02-20

3. Recent progress in the total synthesis of pyrrole-containing natural products (2011–2020);Organic Chemistry Frontiers;2021

4. Reactivity of 2-Nitropyrrole Systems: Development of Improved Synthetic Approaches to Nitropyrrole Natural Products;The Journal of Organic Chemistry;2018-10-01

5. Marine natural products;Natural Product Reports;2018

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