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Functionalization of Styrenes by Copper‐Catalyzed Borylation/ ortho ‐Cyanation and Silver‐Catalyzed Annulation Processes
Author(s) -
Zhao Wanxiang,
Montgomery John
Publication year - 2015
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201507303
Subject(s) - cyanation , hydroboration , borylation , alkene , annulation , catalysis , selectfluor , chemistry , combinatorial chemistry , surface modification , organic chemistry , aryl , alkyl
An efficient two‐step method for the assembly of indanone derivatives starting from a simple vinyl arene has been developed. The sequence first involves addition of bis(pinacolato)diboron (B 2 pin 2 ) and N ‐cyano‐ N ‐phenyl‐ p ‐methylbenzenesulfonamide (NCTS) to a broad range of styrenes by utilizing IMesCuCl as catalyst. This step simultaneously accomplishes hydroboration of the alkene and ortho cyanation of the benzene unit. The products thus obtained are further functionalized by a AgNO 3 /Selectfluor‐mediated coupling of the BPin and cyano functionalities to annulate a new five‐membered ring. This combined two‐step sequence provides a versatile method for the site‐selective derivatization of a broad range of vinyl arene substrates.