Synthetic and structural studies of key intermediates toward forskolin and/or erigerol. Relative stereochemistry, conformational preferences and stereoselectivity control-Reference-Cited by-同舟云学术

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Synthetic and structural studies of key intermediates toward forskolin and/or erigerol. Relative stereochemistry, conformational preferences and stereoselectivity control

Published:1993 Issue:17 Volume: Page:2009-2015
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Bacigaluppo José A.,Colombo María I.,González-Sierra Manuel,Preite Marcelo D.,Zinczuk Juan,Rúveda Edmundo A.,Duddeck Helmut,Hiegemann Monika

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1993/P1/P19930002009

Reference28 articles.

1. Structures and stereochemistry of new labdane diterpiniods from coleus forskohlii briq.

2. Synthetic routes to forskolin

3. Cardiovascular effects of new water-soluble derivatives of forskolin

4. Using the Principles of ORGANIC CHEMISTRY to Explore CELL BIOLOGY

Cited by 2 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. ChemInform Abstract: Synthetic and Structural Studies of Key Intermediates Towards Forskolin and/or Erigerol. Relative Stereochemistry, Conformational Preferences and Stereoselectivity Control.;ChemInform;2010-08-19

2. Synthesis of the Ziegler Key Intermediate and Related Precursors for the Synthesis of Forskolin and Erigerol in Enantiomerically Pure Form;Synthetic Communications;1994-10

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