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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Pyrrolidines and Piperidines by Ligand-Enabled Aza-Heck Cyclizations and Cascades of N-(Pentafluorobenzoyloxy)carbamates

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Author(s):
Hazelden, Ian R. [1] ; Carmona, Rafaela C. [1] ; Langer, Thomas [2] ; Pringle, Paul G. [1] ; Bower, John F. [1]
Total Authors: 5
Affiliation:
[1] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon - England
[2] AstraZeneca, Pharmaceut Technol & Dev, Charter Way, Macclesfield SK10 2NA, Cheshire - England
Total Affiliations: 2
Document type: Journal article
Source: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION; v. 57, n. 18, p. 5124-5128, APR 23 2018.
Web of Science Citations: 8
Abstract

Ligand-enabled aza-Heck cyclizations and cascades of N-(pentafluorobenzoyloxy)carbamates are described. These studies encompass the first examples of efficient non-biased 6-exo aza-Heck cyclizations. The methodology provides direct and flexible access to carbamate protected pyrrolidines and piperidines. (AU)

FAPESP's process: 16/00422-0 - Enantioselective construction of C-N bond by means of the Narasaka-Heck reaction
Grantee:Rafaela Costa Carmona
Support Opportunities: Scholarships abroad - Research Internship - Doctorate