Diastereoselective Synthesis of Cularine Alkaloids via Enium Ions and an Easy Entry to Isoquinolines by Aza-Wittig Electrocyclic Ring Closure-Reference-Cited by-同舟云学术

Diastereoselective Synthesis of Cularine Alkaloids via Enium Ions and an Easy Entry to Isoquinolines by Aza-Wittig Electrocyclic Ring Closure

Published:2004-04-01 Issue:9 Volume:69 Page:2920-2928
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Rodrigues J. Augusto R.¹,Abramovitch Rudolph A.¹,de Sousa Joana D. F.¹,Leiva Genaro C.¹

Affiliation:

1. Universidade Estadual de Campinas, Instituto de Quimica, 13.083-970 Campinas, Brazil, and Department of Chemistry, Clemson University, Clemson, South Carolina 29634-0973

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo030287t

Reference50 articles.

1. THE ALKALOIDS OF FUMARIACEOUS PLANTS: XXVI. CORYDALIS CLAVICULATA (L.) DC.

2. The Alkaloids of Fumariaceous Plants. XLIII. The Structures of Cularine and of Cularimine

3. New Isoquinoline Alkaloids from Corydalis claviculata

4. Alkaloids from Sarcocapnos saetabensis

5. Alkaloids from Ceratocapnos heterocarpa plants and in vitro cultures

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