Nucleophilic Addition of 1-Acetylindole Enolates to Pyridinium Salts. Stereoselective Formal Synthesis of (±)-Geissoschizine and (±)-Akagerine via 1,4-Dihydropyridines-Reference-Cited by-同舟云学术

Nucleophilic Addition of 1-Acetylindole Enolates to Pyridinium Salts. Stereoselective Formal Synthesis of (±)-Geissoschizine and (±)-Akagerine via 1,4-Dihydropyridines

Published:1999-12-01 Issue:26 Volume:64 Page:9605-9612
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Bennasar M.-Lluïsa¹,Jiménez Juan-Miguel¹,Vidal Bernat¹,Sufi Bilal A.¹,Bosch Joan¹

Affiliation:

1. Laboratory of Organic Chemistry, Faculty of Pharmacy, University of Barcelona, Barcelona 08028, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9911894

Reference53 articles.

1. General method for the synthesis of bridged indole alkaloids. Nucleophilic addition of indoleacetic ester enolates to N-alkylpyridinium salts

2. Studies on the synthesis of mavacurine-type indole alkaloids. First total synthesis of (±)-2,7-dihydropleiocarpamine

3. Nucleophilic addition of indole-2-acetic ester enolates to N-alkylpyridinium salts. A formal synthesis of the strychnos alkaloids tubifolidine and tubifoline

4. A new synthetic entry to pentacyclic Strychnos alkaloids. Total synthesis of (.+-.)-tubifolidine, (.+-.)-tubifoline, and (.+-.)-19,20-dihydroakuammicine

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