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Heck Reactions with Metals Other than Palladium

Mizoroki-Heck Reactions with Metals Other than Palladium [Pg.383]

Institutfiir Organische und Biomolekulare Chemie, Georg-August-Universitdt, Tammannstralie 2, [Pg.383]

The Mizoroki-Heck Reaction Edited by Martin Oestreich 2009 John Wiley Sons. Ltd. ISBN 978-0-470-03394-4 [Pg.383]

As the detailed mechanism of various metal-catalysed reactions discussed below is often not well understood, a phenomenological presentation is provided, which is categorized according to the transition metal employed. [Pg.384]

Copper salts are well known to mediate or catalyse a variety of valuable C-C and C-heteroatom bond forming reactions with numerous electrophiles [17,18]. Furthermore, they are generally relatively inexpensive, a beneficial asset compared with the well-established palladium-based catalysts. [Pg.384]

Herein, a survey of the literature up to mid 2007 is provided, covering catalytic arylation and alkenylation reactions of alkenes with metals other than palladium. The review summarizes Mizoroki-Heck-type reactions employing organic (pseudo)halides as electrophiles (Scheme 10.1), while oxidative Mizoroki-Heck-type reactions [6] are beyond the scope of this review (Chapters 4 and 9). Valuable transition-metal-catalysed arylation reactions of alkenes employing stoichiometric amounts of organometallic compounds as... [Pg.383]

See other pages where Heck Reactions with Metals Other than Palladium is mentioned: [Pg.383]    [Pg.393]    [Pg.400]    [Pg.895]    [Pg.209]    [Pg.451]    [Pg.664]    [Pg.82]    [Pg.46]    [Pg.175]    [Pg.891]    [Pg.740]    [Pg.109]    [Pg.58]    [Pg.1336]    [Pg.16]    [Pg.451]    [Pg.82]    [Pg.365]    [Pg.334]   


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Metal palladium

Metallic palladium

Other metals

Reaction with palladium

With palladium

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