Tetraarylphosphonium Halides as Arylating Reagents in Pd??Catalyzed Heck and Cross??Coupling Reactions

LK Hwang, Y Na, J Lee, Y Do…

Index: Hwang, Lee Kyoung; Na, Youngim; Lee, Junseong; Do, Youngkyu; Chang, Sukbok Angewandte Chemie - International Edition, 2005 , vol. 44, # 38 p. 6166 - 6169

Full Text: HTML

Citation Number: 50

Abstract

Transition-metal-catalyzed olefination and cross-coupling reactions have become one of the most powerful tools in organic synthesis.[1] While aryl, alkenyl, alkynyl, and, more recently, alkyl halides are typically employed as coupling reagents, a variety of different types of pseudohalide species have been also investigated as useful electrophiles. Among these, representative recent examples are carboxylic acids,[2] acid anhydrides,[3] aryl esters,[4] ...

 Related Synthetic Route

~77%

Learn More

~85%

Learn More

~95%

Learn More

~75%

Learn More

~83%

Learn More

~76%

Learn More

~71%

Learn More

~79%

Learn More

~70%

Learn More

~69%

Learn More

~73%

Learn More

~78%

Learn More

~98%

Learn More

~71%

Learn More

~60%

Learn More

~98%

Learn More

~98%

Learn More