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Journal article

DABSO-based, three-component, one-pot sulfone synthesis.

Abstract:
The addition of Grignard reagents or organolithium reagents to the SO2-surrogate DABSO generates a diverse set of metal sulfinates, suitable for direct conversion to sulfone products. The metal sulfinates can be trapped in situ with a wide range of C-electrophiles, including alkyl, allyl, and benzyl halides, epoxides, and (hetero)aryliodoniums.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1021/ol403122a

Authors

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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author


Publisher:
American Chemical Society
Journal:
Organic letters More from this journal
Volume:
16
Issue:
1
Pages:
150-153
Publication date:
2013-12-01
DOI:
EISSN:
1523-7052
ISSN:
1523-7060


Language:
English
Keywords:
Pubs id:
441788
UUID:
uuid:58324890-5cff-4d41-bc8c-ac98e7afb76c
Local pid:
pubs:441788
Source identifiers:
441788
Deposit date:
2014-01-30
ARK identifier:

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