Total Synthesis of the Strychnos Alkaloids (±)-Akuammicine and (±)-Norfluorocurarine from 3a-(o-Nitrophenyl)hexahydroindol-4-ones by Nickel(0)-Promoted Double Cyclization-Reference-Cited by-同舟云学术

Total Synthesis of the Strychnos Alkaloids (±)-Akuammicine and (±)-Norfluorocurarine from 3a-(o-Nitrophenyl)hexahydroindol-4-ones by Nickel(0)-Promoted Double Cyclization

Published:1996-01-01 Issue:13 Volume:61 Page:4194-4195
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Solé, Daniel¹,Bonjoch Josep¹,Bosch Joan¹

Affiliation:

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

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo960588l

Reference20 articles.

1. A new, general synthetic pathway to Strychnos indole alkaloids. First total synthesis of (.+-.)-echitamidine

2. Synthesis applications of cationic aza-Cope rearrangements. 24. The aza-Cope-Mannich approach to Strychnos alkaloids. Short stereocontrolled total syntheses of (.+-.)-dehydrotubifoline and (.+-.)-akuammicine

3. Studies on the Synthesis of Strychnos Indole Alkaloids. Synthesis of (.+-.)-Dehydrotubifoline

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