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Atom‐Efficient Vinylic Arylations with Triarylbismuths as Substoichiometric Multicoupling Reagents under Palladium Catalysis
Author(s) -
Rao Maddali L. N.,
Jadhav Deepak N.,
Venkatesh Varadhachari
Publication year - 2009
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.200900487
Subject(s) - chemistry , palladium , reagent , catalysis , palladium catalyst , atom (system on chip) , atom economy , organic chemistry , combinatorial chemistry , medicinal chemistry , computer science , embedded system
The first atom‐efficient arylation of vinylic iodides was achieved by using triarylbismuths as substoichiometric multicoupling reagents under palladium catalysis. Vinylic iodides were efficiently coupled with electronically divergent triarylbismuths to furnish the corresponding arylated products in short reaction times. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)