π-Aromatic and Sulfur Nucleophilic Partners in Cationic π-Cyclizations: Intramolecular Amidoalkylation and Thioamidoalkylation Cyclization via ω-Carbinol Lactams1,2-Reference-Cited by-同舟云学术

π-Aromatic and Sulfur Nucleophilic Partners in Cationic π-Cyclizations: Intramolecular Amidoalkylation and Thioamidoalkylation Cyclization via ω-Carbinol Lactams1,2

Published:2001-05-26 Issue:13 Volume:66 Page:4695-4703
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hucher Nicolas¹,Decroix Bernard¹,Daïch Adam¹

Affiliation:

1. Laboratoire de Chimie, URCOM, Faculté des Sciences & Techniques de l'Université du Havre, 25, rue Philippe Lebon, B.P: 540, F-76058 Le Havre Cedex, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0156316

Reference36 articles.

1. This work was presented in part at the XVIIIth European Colloquium on Heterocyclic Chemistry (ECHC 98), Rouen, France, October 4−7, 1998.

2. This work was also presented at the American Chemical Society National Meeting, Poster 367, San Francisco, CA, March 26−30, 2000.

3. Allenic amino acids. 1. Synthesis of .gamma.-allenic GABA by a novel aza-Cope rearrangement

4. N-Acyliminium ion rearrangements: generalities and application to the synthesis of pyrrolizidine alkaloids

5. Recent developments in alkaloid synthesis

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