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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(Preview, Version of record, pdf, 1.6MB, Terms of use)
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- Publisher copy:
- 10.1021/acs.orglett.3c04030
Authors
+ Engineering and Physical Sciences Research Council
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
Terms of use
- Copyright holder:
- McNamee et al.
- Copyright date:
- 2023
- Rights statement:
- © 2023 The Authors. Published by American Chemical Society. This publication is licensed under CC-BY 4.0.
- Licence:
- CC Attribution (CC BY)
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