In:
Bulletin of the Chemical Society of Japan, Oxford University Press (OUP), ( 2024-01-18)
Abstract:
The regioselectivity in the sulfonium-mediated arylation of phenols with aryl sulfoxide is significantly influenced by the substituents at the 2 position of phenols. While most substituents tend to promote the expected C–C bond formation at the 6 position, alkyl substituents induce the minor formation of rearranged biaryls, the 1,2,3-substituted isomers.
Type of Medium:
Online Resource
ISSN:
0009-2673
,
1348-0634
DOI:
10.1093/bulcsj/uoae002
Language:
English
Publisher:
Oxford University Press (OUP)
Publication Date:
2024
detail.hit.zdb_id:
2041163-7
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