Enantioselective synthesis of isoquinoline alkaloids
- 1 November 1986
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 64 (11) , 2205-2210
- https://doi.org/10.1139/v86-363
Abstract
The utility of the Pictet–Spengler condensation of (R)-(+)-glyceraldehyde with dopamine hydrochloride in the enantioselective synthesis of isoquinoline alkaloids is demonstrated by the preparation of (S)-(−)-carnegine, (R)-(−)-calycotomine, and (S)-(+)-laudanosine.This publication has 2 references indexed in Scilit:
- Pictet–Spengler reaction of biogenic amines with carbohydrates. Synthesis of novel C-nucleosidesCanadian Journal of Chemistry, 1983
- Models of folate coenzymes-IXTetrahedron, 1983