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Decarboxylative Borylation of m CPBA-Activated Aliphatic Acids
A decarboxylative borylation of aliphatic acids for the synthesis of a variety of alkylboronates has been developed by mixing -chloroperoxybenzoic acid ( CPBA)-activated fatty acids with bis(catecholato)diboron in , -dimethylformamide (DMF) at room temperature. A radical chain process is involved in...
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Published in: | Organic letters 2020-01, Vol.22 (1), p.234-238 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A decarboxylative borylation of aliphatic acids for the synthesis of a variety of alkylboronates has been developed by mixing
-chloroperoxybenzoic acid (
CPBA)-activated fatty acids with bis(catecholato)diboron in
,
-dimethylformamide (DMF) at room temperature. A radical chain process is involved in the reaction which initiates from the B-B bond homolysis followed by the radical transfer from the boron atom to the carbon atom with subsequent decarboxylation and borylation. |
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ISSN: | 1523-7060 1523-7052 |
DOI: | 10.1021/acs.orglett.9b04218 |