Issue 42, 2014

Silver-catalyzed carbonphosphonation of α,α-diaryl allylic alcohols: synthesis of β-aryl-γ-ketophosphonates

Abstract

Silver-catalyzed carbonphosphonation of α,α-diaryl allylic alcohols is achieved. A series of γ-ketophosphonates with different substituents were readily obtained. The mechanistic study indicated that the reaction was initiated by the addition of P-radicals, which sequentially undergo 1,2-migration of an aryl group to form C(Ar)–C(sp3) bonds.

Graphical abstract: Silver-catalyzed carbonphosphonation of α,α-diaryl allylic alcohols: synthesis of β-aryl-γ-ketophosphonates

Supplementary files

Article information

Article type
Communication
Submitted
14 Aug 2014
Accepted
09 Sep 2014
First published
09 Sep 2014

Org. Biomol. Chem., 2014,12, 8394-8397

Silver-catalyzed carbonphosphonation of α,α-diaryl allylic alcohols: synthesis of β-aryl-γ-ketophosphonates

X. Mi, C. Wang, M. Huang, Y. Wu and Y. Wu, Org. Biomol. Chem., 2014, 12, 8394 DOI: 10.1039/C4OB01739K

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