Total synthesis of (15S, 16R, 19S, 20R, 34S)-diepomuricanin-Reference-Cited by-同舟云学术

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Total synthesis of (15S, 16R, 19S, 20R, 34S)-diepomuricanin

Published:1996-07 Issue:30 Volume:37 Page:5393-5396
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Konno Hiroyuki,Makabe Hidefumi,Tanaka Akira,Oritani Takayuki

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

1. Annonaceous Acetogenins: A Review

2. Annonaceous acetogenins: An updated review

3. Annonaceous acetogenins: An updated review—appendices

4. Phytochemical Potential of Tropical Plants;Cave,1993

5. Annonaceous Acetogenins: Potent Mitochondrial Inhibitors with Diverse Applications;Gu,1995

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1. Muricatacin, a Gateway Molecule to Higher Acetogenin Synthesis;Chemistry – An Asian Journal;2020-10-09

2. Applications of sharpless asymmetric dihydroxylation in the total synthesis of natural products;Tetrahedron: Asymmetry;2017-08

3. Total Synthesis of Muricadienin, the Putative Key Precursor in the Solamin Biosynthesis;Organic Letters;2014-11-07

4. ChemInform Abstract: Synthetic Studies on Annonaceous Acetogenins. Part 6. Total Synthesis of (15S,16R,19S,20R,34S)-Diepomuricanin (X).;ChemInform;2010-08-04

5. A chiron approach to the total synthesis of cytotoxic (+)-muricatacin and (+)-5-epi-muricatacin from d-ribose;Carbohydrate Research;2010-01

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