Regioselective transition-metal-free oxidative cyclobutanol ring expansion to 4-tetralones
File(s)20181123_1336_Ring_expansion_paper.docx (3.55 MB)
Accepted version
Author(s)
Natho, Philipp
Kapun, Mia
Allen, Lewis
Parsons, Philip J
Type
Journal Article
Abstract
A facile and transition-metal-free ring expansion of the cyclobutanol moiety to 4-tetralones fused to heteroaromatic systems is described. The oxidative ring expansion proceeds rapidly and regioselectively through mediation by N-bromosuccinimide and acetonitrile in satisfactory to good yields. The preparation of precursors, as well as the ring expansion have proven to be scalable and are straightforward to carry out
Date Issued
2018-12-21
Date Acceptance
2018-12-04
Citation
Organic Letters, 2018, 20 (24), pp.8030-8034
ISSN
1523-7052
Publisher
American Chemical Society
Start Page
8030
End Page
8034
Journal / Book Title
Organic Letters
Volume
20
Issue
24
Copyright Statement
© 2018 American Chemical Society
Sponsor
Imperial College Trust
Grant Number
N/A
Subjects
Science & Technology
Physical Sciences
Chemistry, Organic
Chemistry
OPENING FUNCTIONALIZATION
REGIOSPECIFIC SYNTHESIS
MIGRATION SEQUENCES
CLEAVAGE
STRATEGY
KETONES
03 Chemical Sciences
Organic Chemistry
Publication Status
Published
Date Publish Online
2018-12-06