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Abstract:
Direct functionalization of 1,2-azaborines to construct B-C bonds remains challenging. Here, we report a Pd-catalyzed B-H aryl/alkenylation reaction of 1,2-azaborines. The method provides a general platform to access diverse boron-substituted 1,2-azaborine compounds (>60 examples). The synthetic utility is highlighted through the late-stage modification of bioactive molecules, as well as the preparation and transformations of the B-10-enriched 1,2-azaborine product and the synthesis of four BN isostere analogues of bioactive molecules. And the reaction mechanism is also explored and discussed.
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ACS CATALYSIS
ISSN: 2155-5435
Year: 2024
Issue: 22
Volume: 14
Page: 16996-17003
1 1 . 7 0 0
JCR@2023
Cited Count:
WoS CC Cited Count: 3
SCOPUS Cited Count:
ESI Highly Cited Papers on the List: 0 Unfold All
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Chinese Cited Count:
30 Days PV: 0
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