Copper-Catalyzed Cycloisomerization of Unactivated Allene-Tethered O-Propargyl Oximes: A Domino Reaction Sequence toward the Synthesis of Hexahydropyrrolo[3,4-b]azepin-5(4H)-ones-Reference-Cited by-同舟云学术

Copper-Catalyzed Cycloisomerization of Unactivated Allene-Tethered O-Propargyl Oximes: A Domino Reaction Sequence toward the Synthesis of Hexahydropyrrolo[3,4-b]azepin-5(4H)-ones

Published:2021-04-12 Issue:9 Volume:23 Page:3343-3348
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Nikbakht Ali¹²,Amiri Kamran¹²^ORCID,Khosravi Hormoz¹²^ORCID,Zhou Yirong¹,Balalaie Saeed²³^ORCID,Breit Bernhard¹^ORCID

Affiliation:

1. Institut fur Organische Chemie, Albert-Ludwigs-Universitat Freiburg Albertstrasse 21, 79104 Freiburg im Breisgau, Germany

2. Peptide Chemistry Research Center, K. N. Toosi University of Technology, Tehran 15875-4416, Iran

3. Medical Biology Research Center, Kermanshah University of Medical Sciences, Kermanshah 6714415185, Iran

Funder

Alexander von Humboldt-Stiftung

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c00837

Reference46 articles.

1. Stereodynamic properties of medium-ring benzo-fused nitrogenous heterocycles: benzodiazepines, benzazepines, benzazocines, and benzazonines

2. Seven-Membered Rings

3. Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals

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