Stereoselective synthesis of an isoquinolinopyrrolidinone by acyliminium ion cyclization of chiral hydroxylactams

Article abstract of DOI:10.1080/00397919508015871

Studies on the stereoselective synthesis of a pyrrolidinoisoquinoline derivative using acyliminium ion cyclization of hydroxylactams are described. Cyclization reaction of chiral hydroxylactams 2a~c, derived from (L)-tartaric acid and phenethylamine, affo

Full text of DOI:10.1080/00397919508015871

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Synthetic Communications: An
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Stereoselective Synthesis of An
Isoquinolinopyrrolidinone by
Acyliminium Ion Cyclization of
Chiral Hydroxylactams
Yong Sup Lee a , Dong Wook Kang b , Sook Ja Lee b
Hokoon Park a
&
a Organic Chemistry Laboratory (I) , Korea Institute
of Science &Technology , P. O. Box 131 Cheongryang,
Seoul, 130-650, Korea
b Department of Chemistry , Hankook University of
Foreign Studies , Seoul, 130-791, Korea
Published online: 23 Sep 2006.
To cite this article: Yong Sup Lee , Dong Wook Kang , Sook Ja Lee & Hokoon Park
(1995) Stereoselective Synthesis of An Isoquinolinopyrrolidinone by Acyliminium Ion
Cyclization of Chiral Hydroxylactams, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 25:13, 1947-1956,
DOI: 10.1080/00397919508015871
To link to this article: http://dx.doi.org/10.1080/00397919508015871
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