Long-range carbon-proton coupling constants for stereochemical assignment of acyclic structures in natural products: Configuration of the C5C9 portion of maitotoxin-Reference-Cited by-同舟云学术

Long-range carbon-proton coupling constants for stereochemical assignment of acyclic structures in natural products: Configuration of the C5C9 portion of maitotoxin

Published:1996-02 Issue:8 Volume:37 Page:1269-1272
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Matsumori Nobuaki,Nonomura Taro,Sasaki Makoto,Murata Michio,Tachibana Kazuo,Satake Masayuki,Yasumoto Takeshi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

1. Scalar Coupling Constants—Their Analysis and Their Application for the Elucidation of Structures

2. Conformational analysis of natural products using long-range carbon-proton coupling constants: Three-dimensional structure of okadaic acid in solution

3. Some Chemical Properties of Maitotoxin, a Putative Calcium Channel Agonist Isolated from a MarineDinoflagellate1

4. Structure and Partial Stereochemical Assignments for Maitotoxin, the Most Toxic and Largest Natural Non-Biopolymer

5. Synthesis and stereochemical confirmation of the cis-fused L/M and N/O ring systems of maitotoxin

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