Asymmetric synthesis of furo-pyrrolo-isoquinoline and furo-indolizino- indole derivatives via a diastereoselective N-acyliminium ion cyclization

Article abstract of DOI:10.1080/00397919708004155

Asymmetric synthesis of furo-pyrrolo-isoquinoline and furo-indolizino- indole derivatives via a diastereoselective N-acyliminium ion cyclization of chiral enamides is described. The requisite chiral enamides were prepared from readily available L-malic acid.

Full text of DOI:10.1080/00397919708004155

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Synthetic Communications: An
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Organic Chemistry
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Asymmetric Synthesis of Furo-
Pyrrolo-Isoquinoline and Furo-
Indolizino-Indole Derivatives
Via A Diastereoselective N-
Acyliminium ion Cyclization
Yong Sup Lee a , Jae Yeol Lee a & Hokoon Park a
a Division of Applied Science , Korea Institute of
Science & Technology , P. O. Box 131, Cheongryang,
Seoul, 130-650, Korea
Published online: 22 Aug 2006.
To cite this article: Yong Sup Lee , Jae Yeol Lee & Hokoon Park (1997) Asymmetric
Synthesis of Furo-Pyrrolo-Isoquinoline and Furo-Indolizino-Indole Derivatives Via A
Diastereoselective N-Acyliminium ion Cyclization, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 27:16,
2799-2812
To link to this article: http://dx.doi.org/10.1080/00397919708004155
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