Avisible-light driven Suzuki cross-coupling reactionwas per-formed with colored and bench-stable arylazosulfones in thepresenceofPh3PAuCl (5 mol %) as the catalyst.The absence ofaphotocatalyst ,along with the use of commercially availableand easy-to-handle arylboronic acids underline the novelty andsynthetic usefulness of the protocol. Areaction mechanism in-volvingthe generation of an aryl radicalasthe key intermedi-ate has been proposed on the basis of experimental investigations.

Christopher, S., Yang, L., Assunta De Nisi, ., Stefano, P., Maurizio, F., Marco, B. (2017). Photocatalyst-free, Visible Light Driven, Gold PromotedSuzuki Synthesis of (Hetero)biaryls. CHEMCATCHEM, 9, 4456-4459 [10.1002/cctc.201701436].

Photocatalyst-free, Visible Light Driven, Gold PromotedSuzuki Synthesis of (Hetero)biaryls

Yang Liu
Methodology
;
Assunta De Nisi
Investigation
;
Marco Bandini
Supervision
2017

Abstract

Avisible-light driven Suzuki cross-coupling reactionwas per-formed with colored and bench-stable arylazosulfones in thepresenceofPh3PAuCl (5 mol %) as the catalyst.The absence ofaphotocatalyst ,along with the use of commercially availableand easy-to-handle arylboronic acids underline the novelty andsynthetic usefulness of the protocol. Areaction mechanism in-volvingthe generation of an aryl radicalasthe key intermedi-ate has been proposed on the basis of experimental investigations.
2017
Christopher, S., Yang, L., Assunta De Nisi, ., Stefano, P., Maurizio, F., Marco, B. (2017). Photocatalyst-free, Visible Light Driven, Gold PromotedSuzuki Synthesis of (Hetero)biaryls. CHEMCATCHEM, 9, 4456-4459 [10.1002/cctc.201701436].
Christopher, Sauer; Yang, Liu; Assunta De Nisi, ; Stefano, Protti; Maurizio, Fagnoni; Marco, Bandini
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/614823
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