Catalytic arylation methods: from the academic lab to industrial processes

by Burke, Anthony J., (Anthony Joseph)

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Title Statements

Full title :Catalytic arylation methods : from the academic lab to industrial processes / Anthony J. Burke and Carolina Silva Marques.

Edition Statements

Publication Date:©2015
Edition:First edition

Publication Statements

Publisher(s):Wiley-VCH Verlag GmbH & Co. KGaA
Place of Publication:Weinheim, Germany
Language:eng
Publication Date:©2015

The Physical Object

Description:xix, 502 pages : : illustrations (some colour) ; : 25 cm

Edition Identifiers

ISBN:9783527335183, 3527335188
oclc:ocn903161695
LC Classification:QD505
Dewey Decimal:541.395

1.1.Metal-Catalyzed Cross-Couplings: From Its Origins to the Nobel Prize and Beyond -- 1.2.Arylation: What Is So Special? -- 1.3.Recent New Developments -- 1.3.1.Arylations with the Heck[--]Mizoroki Reaction -- 1.3.2.Arylations with the Heck[--]Matsuda Reaction[--]Recent Developments -- 1.3.3.Hiyama[--]Hatanaka Cross-Coupling Reaction -- 1.3.4.Arylations with the Stille Reaction -- 1.3.5.Arylations with the Sonogashira[--]Hagihara Reaction -- 1.3.6.Arylations with the Suzuki[--]Miyaura Reaction -- 1.3.7.Tamao[--]Kumada[--]Corriu Cross Coupling -- 1.3.8.Negishi-Baba Cross-Coupling -- 1.3.9.Beyond the Ullmann and Suzuki[--]Miyaura Reactions, Other Newer Approaches to Functional Biaryl Synthesis: Pd, Fe, Co, and Other Metals -- 1.3.9.1.With Palladium -- 1.3.9.2.With Iron -- 1.3.9.3.With Nickel -- 1.3.9.4.With Cobalt -- 1.3.10.Conclusions -- 1.4.Selected Experiments from the Literature -- 1.4.1.The Heck[--]Mizoroki Reaction -- 1.4.1.1.Heterogeneous Catalytic Synthesis of (E)-Butyl Cinnamate Using a Palladium Nanosphere Catalyst -- 1.4.1.2.The Preparative Catalytic Synthesis of 5-(p-Trifluoromethylphenyl)-2,3-dihydrofuran in Continuous Flow -- 1.4.2.The Heck[--]Matsuda Reaction -- 1.4.…