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Journal article

Bridge cross-coupling of bicyclo[1.1.0]butanes

Abstract:
Bicyclo[1.1.0]butanes (BCBs) have gained growing popularity in “strain release” chemistry for the synthesis of four-membered-ring systems and para- and meta-disubstituted arene bioisosteres as well as applications in chemoselective bioconjugation. However, functionalization of the bridge position of BCBs can be challenging due to the inherent strain of the ring system and reactivity of the central C–C bond. Here we report the first late-stage bridge cross-coupling of BCBs, mediated by directed metalation/palladium catalysis.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1021/acs.orglett.3c04030

Authors


More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Oxford college:
Jesus College
Role:
Author
ORCID:
0000-0002-4149-0494


More from this funder
Funder identifier:
https://ror.org/0439y7842
Grant:
EP/S013172/1
EP/L015838/1


Publisher:
American Chemical Society
Journal:
Organic Letters More from this journal
Volume:
26
Issue:
1
Pages:
360-364
Place of publication:
United States
Publication date:
2023-12-29
Acceptance date:
2023-12-20
DOI:
EISSN:
1523-7052
ISSN:
1523-7060
Pmid:
38156902


Language:
English
Pubs id:
1595032
Local pid:
pubs:1595032
Deposit date:
2024-06-24

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