%0 Journal Article
%T Catalysis in the service of green chemistry: Nobel prize-winning palladium-catalysed cross-couplings, run in water at room temperature
%A Lipshutz, B.H.
%A Taft, B.R.
%A Abela, A.R.
%A Ghorai, S.
%A Krasovskiy, A.
%A Duplais, C.
%J Platinum Metals Review
%D 2012
%V 56
%N 2
%@ 00321400 (Issn)
%F Lipshutz_etal2012
%O Cited By (since 1996): 1; Export Date: 15 May 2012; Source: Scopus; Coden: Ptmra; doi: 10.1595/147106712X629761; Language of Original Document: English; Correspondence Address: Lipshutz, B.H.; Department of Chemistry, University of California, Santa Barbara, CA 93106, United States; email: lipshutz@chem.ucsb.edu
%O exported from refbase (http://php.ecofog.gf/refbase/show.php?record=400), last updated on Tue, 15 May 2012 12:17:06 -0300
%X Palladium-catalysed cross-couplings, in particular Heck, Suzuki-Miyaura and Negishi reactions developed over three decades ago, are routinely carried out in organic solvents. However, alternative media are currently of considerable interest given an increasing emphasis on making organic processes 'greener'; for example, by minimising organic waste in the form of organic solvents. Water is the obvious leading candidate in this regard. Hence, this review focuses on the application of micellar catalysis, in which a 'designer' surfactant enables these award-winning coupling reactions to be run in water at room temperature. © 2012 Johnson Matthey.
%U http://www.scopus.com/inward/record.url?eid=2-s2.0-84860442545&partnerID=40&md5=e088599689a72c208950fdd5c74a77dd
%U http://php.ecofog.gf/refbase/files/lipshutz/2012/400_Lipshutz_etal2012.pdf
%P 62-74