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Martin Oestreich - The Mizoroki-Heck Reaction - 9780470033944 - V9780470033944
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The Mizoroki-Heck Reaction

€ 196.91
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Description for The Mizoroki-Heck Reaction Hardcover. Exploring the importance of Richard F. Heck's carbon coupling reaction, this book highlights the subject of the 2010 Nobel Prize in Chemistry for palladium-catalyzed cross couplings in organic synthesis, and includes a foreword from Nobel Prize winner Richard F. Heck. Editor(s): Oestreich, Martin. Num Pages: 608 pages, Illustrations. BIC Classification: PNN. Category: (P) Professional & Vocational; (UP) Postgraduate, Research & Scholarly. Dimension: 246 x 172 x 39. Weight in Grams: 1158.
Exploring the importance of Richard F. Heck’s carbon coupling reaction, this book highlights the subject of the 2010 Nobel Prize in Chemistry for palladium-catalyzed cross couplings in organic synthesis, and includes a foreword from Nobel Prize winner Richard F. Heck.

The Mizoroki-Heck reaction is a palladium-catalyzed carbon–carbon bond forming process which is widely used in organic and organometallic synthesis. It has seen increasing use in the past decade as chemists look for strategies enabling the controlled construction of complex carbon skeletons. The Mizoroki-Heck Reaction is the first dedicated volume on this important reaction, including topics on:

  • mechanisms of the ... Read more
  • intermolecular Mizoroki-Heck reactions
  • focus on regioselectivity and product outcome in organic synthesis
  • waste-minimized Mizoroki-Heck reactions
  • intramolecular Mizoroki-Heck reactions
  • formation of heterocycles
  • chelation-controlled Mizoroki-Heck reactions
  • the Mizoroki-Heck reaction in domino processes
  • oxidative heck-type reactions (Fujiwara-Moritani reactions)
  • Mizoroki-Heck reactions with metals other than palladium
  • ligand design for intermolecular asymmetric Mizoroki-Heck reactions
  • intramolecular enantioselective Mizoroki-Heck reactions
  • desymmetrizing Mizoroki-Heck reactions
  • applications in combinatorial and solid phase syntheses, and the development of modern solvent systems and reaction techniques
  • the asymmetric intramolecular Mizoroki-Heck reaction in natural product total synthesis

Several chapters are devoted to asymmetric Heck reactions with particular focus on the construction of otherwise difficult-to-obtain sterically congested tertiary and quaternary carbons. Industrial and academic applications are highlighted in the final section. The Mizoroki-Heck Reaction will find a place on the bookshelves of any organic or organometallic chemist.

“I am convinced that this book will rapidly become the most important reference text for research chemists in academia and industry who seek orientation in the rapidly growing and – for the layman – confusing field described as the “’Mizoroki–Heck reaction’.” (Synthesis, March 2010)

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Product Details

Format
Hardback
Publication date
2009
Publisher
John Wiley & Sons Inc United Kingdom
Number of pages
608
Condition
New
Number of Pages
608
Place of Publication
New York, United States
ISBN
9780470033944
SKU
V9780470033944
Shipping Time
Usually ships in 7 to 11 working days
Ref
99-50

About Martin Oestreich
Martin Oestreich (born in 1971 in Pforzheim/Germany) is currently Professor of Organic Chemistry at the Technische Universität Berlin. He received his diploma degree with Paul Knochel (Marburg, 1996) and his doctoral degree with Dieter Hoppe (Münster, 1999). After a two-year postdoctoral stint with Larry E. Overman (Irvine, 1999-2001), he completed his habilitation with Reinhard Brückner (Freiburg, 2001-2005) and was appointed ... Read more

Reviews for The Mizoroki-Heck Reaction
"It is by far the most authoritative book in this area written to date and has employed many of the major contributors in the area over recent years to provide chapters, resulting in good...coverage of the literature." (Applied Organimetallic Chemistry , March 2010) “I am convinced that this book will rapidly become the most important reference ... Read more

Goodreads reviews for The Mizoroki-Heck Reaction


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