Investigation of Carbon-nitrogen Double Bonds in the Intramolecular Ene Reaction
Title | Investigation of Carbon-nitrogen Double Bonds in the Intramolecular Ene Reaction PDF eBook |
Author | Jyh-Ming Lin |
Publisher | |
Pages | 234 |
Release | 1985 |
Genre | Alkenes |
ISBN |
The Chemistry of the Carbon-nitrogen Double Bond
Title | The Chemistry of the Carbon-nitrogen Double Bond PDF eBook |
Author | Saul Patai |
Publisher | |
Pages | 816 |
Release | 1970 |
Genre | Science |
ISBN |
The Kinetic Studies of Intramolecular Nucleophilic Substitution at Carbon-nitrogen Double Bond ...
Title | The Kinetic Studies of Intramolecular Nucleophilic Substitution at Carbon-nitrogen Double Bond ... PDF eBook |
Author | Yi Li |
Publisher | |
Pages | 100 |
Release | 1995 |
Genre | Carbon compounds |
ISBN |
Dissertation Abstracts International
Title | Dissertation Abstracts International PDF eBook |
Author | |
Publisher | |
Pages | 862 |
Release | 1999 |
Genre | Dissertations, Academic |
ISBN |
Studies on the Intramolecular Ene Reaction of Cyclopropenes and Related Systems
Title | Studies on the Intramolecular Ene Reaction of Cyclopropenes and Related Systems PDF eBook |
Author | Robert Joseph Rosenthal |
Publisher | |
Pages | 530 |
Release | 1982 |
Genre | Chemical reactions |
ISBN |
Stereoselective Organocatalysis
Title | Stereoselective Organocatalysis PDF eBook |
Author | Ramon Rios Torres |
Publisher | John Wiley & Sons |
Pages | 581 |
Release | 2013-04-29 |
Genre | Science |
ISBN | 1118604709 |
Sets forth an important group of environmentally friendly organic reactions With contributions from leading international experts in organic synthesis, this book presents all the most important methodologies for stereoselective organocatalysis, fully examining both the activation mode as well as the type of bond formed. Clear explanations guide researchers through all the most important methods used to form key chemical bonds, including carbon-carbon (C–C), carbon-nitrogen (C–N), and carbon-halogen (C–X) bonds. Moreover, readers will discover how the use of non-metallic catalysts facilitates a broad range of important reactions that are environmentally friendly and fully meet the standards of green chemistry. Stereoselective Organocatalysis begins with an historical overview and a review of activation modes in asymmetric organocatalysis. The next group of chapters is organized by bond type, making it easy to find bonds according to their applications. The first of these chapters takes a detailed look at the many routes to C–C bond formation. Next, the book covers: Organocatalytic C–N bond formation C–O bond formation C–X bond formation C–S, C–Se, and C–B bond formation Enantioselective organocatalytic reductions Cascade reactions forming both C–C bonds and C–heteroatom bonds The final chapter is devoted to the use of organocatalysis for the synthesis of natural products. All the chapters in the book are extensively referenced, serving as a gateway to the growing body of original research reports and reviews in the field. Based on the most recent findings and practices in organic synthesis, Stereoselective Organocatalysis equips synthetic chemists with a group of organocatalytic reactions that will help them design green reactions and overcome many challenges in organic synthesis.
Organic Reaction Mechanisms 1986
Title | Organic Reaction Mechanisms 1986 PDF eBook |
Author | A. C. Knipe |
Publisher | John Wiley & Sons |
Pages | 616 |
Release | 2008-04-30 |
Genre | Science |
ISBN | 0470066768 |
The only book series to summarize the latest progress on organic reaction mechanisms, Organic Reaction Mechanisms, 1986 surveys the development in understanding of the main classes of organic reaction mechanisms reported in the primary scientific literature in 1986. The 22nd annual volume in this highly successful series highlights mechanisms of stereo-specific reactions. Reviews are compiled by a team of experienced editors and authors, allowing advanced undergraduates, graduate students, postdocs, and chemists to rely on the volume's continuing quality of selection and presentation.