Synthesis of 3-aryl-3-sulfanyl azetidines by iron-catalyzed thiol alkylation with N-Cbz azetidinols
File(s)MS Azetidine Sulfides JOC revised submission.pdf (842.94 KB)
Accepted version
Author(s)
Dubois, Maryne AJ
Lazaridou, Anna
Choi, Chulho
Mousseau, James J
Bull, James A
Type
Journal Article
Abstract
New small-ring derivatives can provide valuable motifs in new chemical space for drug design. 3-Aryl-3-sulfanyl azetidines are synthesized directly from azetidine-3-ols in excellent yield by a mild Fe-catalyzed thiol alkylation. A broad range of thiols and azetidinols bearing electron-donating aromatics are successful, proceeding via an azetidine carbocation. The N-carboxybenzyl group is a requirement for good reactivity and enables the NH-azetidine to be revealed. Further reactions of the azetidine sulfides demonstrate their potential for incorporation in drug discovery programs.
Date Issued
2019-05-03
Date Acceptance
2019-04-01
Citation
The Journal of Organic Chemistry, 2019, 84 (9), pp.5943-5956
ISSN
0022-3263
Publisher
American Chemical Society
Start Page
5943
End Page
5956
Journal / Book Title
The Journal of Organic Chemistry
Volume
84
Issue
9
Copyright Statement
© 2019 American Chemical Society. This document is the Accepted Manuscript version of a Published Work that appeared in final form in The Journal of Organic Chemistry, after peer review and technical editing by the publisher. To access the final edited and published work see https://dx.doi.org/10.1021/acs.joc.9b00613
Sponsor
Engineering & Physical Science Research Council (EPSRC)
The Royal Society
The Royal Society
The Royal Society
Identifier
https://www.ncbi.nlm.nih.gov/pubmed/30973723
Grant Number
EP/J001538/1
UF140161
RG150444
RGF\EA\180031
Subjects
0304 Medicinal and Biomolecular Chemistry
0305 Organic Chemistry
0302 Inorganic Chemistry
Organic Chemistry
Publication Status
Published
Coverage Spatial
United States
Date Publish Online
2019-04-11