Asymmetric Total Synthesis of (+)-Apovincamine and a Formal Synthesis of (+)-Vincamine. Demonstration of a Practical “Asymmetric Linkage” between Aromatic Carboxylic Acids and Chiral Acyclic Substrates-Reference-Cited by-同舟云学术

Asymmetric Total Synthesis of (+)-Apovincamine and a Formal Synthesis of (+)-Vincamine. Demonstration of a Practical “Asymmetric Linkage” between Aromatic Carboxylic Acids and Chiral Acyclic Substrates

Published:1997-03-01 Issue:5 Volume:62 Page:1223-1229
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Schultz Arthur G.¹,Malachowski William P.¹,Pan You¹

Affiliation:

1. Department of Chemistry, Rensselaer Polytechnic Institute, Troy, New York 12180-3590

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo961603p

Reference24 articles.

1. Lounasmaa, M.; Toluanen, A. InThe Alkaloids; Cordell, G. A., Ed.; Academic Press: New York, 1992; Vol. 42, pp 1−116.

2. Comparison of the effects of vinpocetine, vincamine, phenytoin, and cinnarizine in a rat model of cerebral ischemia

3. The effects of bromvincamine and vincamine on regional cerebral blood flow and mental functions in patients with multi-infarct dementia

4. An efficient and practical total synthesis of (+)-vincamine from L-aspartic acid

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