Diastereoselective Protonation of Lactam Enolates Derived from (R)-Phenylglycinol. A Novel Asymmetric Route to 4-Phenyl-1,2,3,4-tetrahydroisoquinolines-Reference-Cited by-同舟云学术

Diastereoselective Protonation of Lactam Enolates Derived from (R)-Phenylglycinol. A Novel Asymmetric Route to 4-Phenyl-1,2,3,4-tetrahydroisoquinolines

Published:2000-06-21 Issue:15 Volume:2 Page:2185-2187
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Philippe Nicolas¹,Levacher Vincent¹,Dupas Georges¹,Quéguiner Guy¹,Bourguignon Jean¹

Affiliation:

1. Laboratoire de Chimie Organique Fine et Hétérocyclique UPRES-A 6014, IRCOF-INSA, rue Tesnières B.P 08, F-76131 Mont Saint Aignan Cedex, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol0057939

Reference19 articles.

1. Recent Progress in the Enatioselective Synthesis of Isoquinoline Alkaloids

2. (a) Belvisi, L.; Gennari, C.; Poli, G.; Scolastico, C.; Salom, B.Tetrahedron: Asymmetry1993,4, 273.

3. Synthesis of racemic (+) and (−) N-[methyl-11C]nomifensine, a ligand for evaluation of monoamine re-uptake sites by use of positron emission tomography

4. Synthesis and pharmacological evaluation of some new tetrahydroisoquinoline derivatives inhibiting dopamine uptake and/or possessing a dopaminomimetic property

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