Organic Reactions

Online ISBN: 9780471264187
DOI: 10.1002/0471264180
About this Book
ABOUT ORGANIC REACTIONS
Organic Reactions is a comprehensive collection of important synthetic reactions, together with a critical discussion of the reaction and tables that organize all published examples of the topic reactions. Chapters that focus on reactions of current interest are solicited by the board of editors from leading chemists worldwide. The publication process entails a comprehensive peer-review process, ensuring the high quality and attention to detail for which this series is noted. Organic Reactions currently consists of over 140,000 reactions, and will continue to grow annually.
Organic Reactionsis the definitive resource for synthetic transformations, with an emphasis on preparative aspects. Comprehensive coverage of all examples of a given reaction is provided in tabular form. In addition to providing reaction scope, stereochemical aspects, and side reactions, a selection of representative experimental conditions are given. All chapters represent the highest standard for accuracy and reliability from internationally acclaimed authors and editors.
What's New
Professor Scott Denmark Honored
Wiley congratulates Professor Scott Denmark, the winner of the 2009 RSC Robert Robinson Lectureship.
Professor Denmark, the Editor in Chief of Organic Reactions, won the award for his pioneering work in the areas of Lewis base catalyzed asymmetric processes, cross-coupling reactions based on organosilanols, and tandem cycloadditions using nitroalkenes.
He delivered a series of lectures at locations throughout the UK in November 2009.
Organic Reactions Honored
Wiley congratulates Organic Reactions the 2009 recipient of the ACS Division of History of Chemistry's Chemical Breakthrough Award!
Includes content from Nobel Prize Winner
Richard F. Heck (Chemistry Nobel Prize Winner 2010)
•Palladium-Catalyzed Vinylation of Organic Halides
Wiley publishes the works of 150 laureates in chemistry, for more Nobel Laureate Content click here
