The application of two-dimensional n.m.r. cross relaxation spectroscopy to natural product structure determination: talaromycin B-Reference-Cited by-同舟云学术

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The application of two-dimensional n.m.r. cross relaxation spectroscopy to natural product structure determination: talaromycin B

Published:1983 Issue:16 Volume: Page:864
ISSN:0022-4936
Container-title:Journal of the Chemical Society, Chemical Communications
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Hutton William C.,Phillips Nancy J.,Graden David W.,Lynn David G.

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1983/C3/C39830000864

Cited by 26 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. Carbohydrate-Derived Spiroketals and Spirocyclic Lactones;Topics in Heterocyclic Chemistry;2019

2. The Total Synthesis of Spiroketal-Containing Natural Products;Total Synthesis of Natural Products;2007-02-20

3. Hexulose Derivatives and Lipase-Mediated Diastereomeric Resolution in the Enantiospecific Total Synthesis of (−)-Talaromycins C and E;European Journal of Organic Chemistry;2002-01

4. Chiral building-blocks by chemoenzymatic desymmetrization of 2-ethyl-1,3-propanediol for the preparation of biologically active natural products;Tetrahedron: Asymmetry;1999-02

5. Synthesis of both top and bottom fragments of (-)-talaromycin A through enantiospecific and diastereoselective elaboration of asymmetrized tris (hydroxymethyl)methane;The Journal of Organic Chemistry;1993-03

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