Convergent approach to tetracyclic [ABCE] intermediates in Aspidosperma alkaloids synthesis

Article abstract of DOI:10.1080/00397919208021293

An efficient convergent synthesis of tetracyclic amidoalcohol 5, key intermediate in the synthesis of Aspidosperma alkaloids framework, starting from trans-hexahydrocarbazol-4-one 1 and substituted iodoacetamides 6 was achieved.

Full text of DOI:10.1080/00397919208021293

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Synthetic Communications: An
International Journal for Rapid
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Organic Chemistry
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Convergent Approach
to Tetracyclic [ABCE]
Intermediates in Aspidosperma
Alkaloids Synthesis
M. Dufour a , J.-C. Gramain a , H. P. Husson b , M. E.
Sinibaldi a & Y. Troin a
a Laboratoire de Chimie des Substances Naturelles ,
associé au CNRS, Université Biaise Pascal , 63177,
AUBIERE CEDEX, FRANCE
b Faculté des Sciences Pharmaceutiques et
Biologiques U.R. A. 1310 CNRS , 4, Avenue de
l'Observatoire, 75270, PARIS CEDEX 06, FRANCE
Published online: 23 Sep 2006.
To cite this article: M. Dufour , J.-C. Gramain , H. P. Husson , M. E. Sinibaldi
& Y. Troin (1992) Convergent Approach to Tetracyclic [ABCE] Intermediates in
Aspidosperma Alkaloids Synthesis, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 22:2, 189-200, DOI:
10.1080/00397919208021293
To link to this article: http://dx.doi.org/10.1080/00397919208021293
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