Article ; Online: Z
Chemical communications (Cambridge, England)
2024 Volume 60, Issue 37, Page(s) 4894–4897
Abstract: An efficient method for the radical difunctionalization of aromatic alkynes has been developed, resulting in the synthesis of a range of valuable triarylethenes. This approach utilizes strategically designed aryldiazonium salts with tertiary alcohol ... ...
Abstract | An efficient method for the radical difunctionalization of aromatic alkynes has been developed, resulting in the synthesis of a range of valuable triarylethenes. This approach utilizes strategically designed aryldiazonium salts with tertiary alcohol substitution as bifunctional reagents, along with cost-effective cuprous chloride as a catalyst. The method demonstrates remarkable |
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Language | English |
Publishing date | 2024-05-02 |
Publishing country | England |
Document type | Journal Article |
ZDB-ID | 1472881-3 |
ISSN | 1364-548X ; 1359-7345 ; 0009-241X |
ISSN (online) | 1364-548X |
ISSN | 1359-7345 ; 0009-241X |
DOI | 10.1039/d4cc01315h |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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