An Intramolecular aza-[3 + 3] Annulation Approach to Azaphenalene Alkaloids. Total Synthesis of Myrrhine-Reference-Cited by-同舟云学术

An Intramolecular aza-[3 + 3] Annulation Approach to Azaphenalene Alkaloids. Total Synthesis of Myrrhine

Published:2007-03-01 Issue:7 Volume:72 Page:2476-2484
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Gerasyuto Aleksey I.¹,Hsung Richard P.¹

Affiliation:

1. Division of Pharmaceutical Sciences and Department of Chemistry, University of Wisconsin, Rennebohm Hall, 777 Highland Avenue, Madison, Wisconsin 53705

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo062533h

Reference45 articles.

1. [3 + 3] Cycloadditions and related strategies in alkaloid natural product synthesis

2. A [3+3] Annelation Approach to Tetrahydropyridines

3. A Novel and Highly Stereoselective Intramolecular Formal [3+3] Cycloaddition Reaction of Vinylogous Amides Tethered withα,β-Unsaturated Aldehydes: A Formal Total Synthesis of (+)-Gephyrotoxin

4. A Novel and Highly Stereoselective Approach to Aza-Spirocycles. A Short Total Synthesis of 2-epi-(±)-Perhydrohistrionicotoxin and an Unprecedented Decarboxylation of 2-Pyrones

5. Stereodivergent Total Syntheses of Precoccinelline, Hippodamine, Coccinelline, and Convergine

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