Name Reactions for Homologation, Part 2

"A valuable addition to the literature by any measure and surely will prove its merit in years to come. The new knowledge that arises with its help will be impressive and of great benefit to humankind."
—From the Foreword by E. J. Corey, Nobel Prize Laureate
An invaluable guide to name reactions and reagents for homologations
Name Reactions for Homologations, Part II of Wiley′s Comprehensive Name Reactions series comprises a comprehensive treatise on name reactions for homologations. With contributions from world–recognized authorities in the field, this reference offers an up–to–date, concise compilation of the most commonly used and widely known name reactions and reagents. Part II discusses Rearrangements, Asymmetric C–C Bond Formation, and Miscellaneous Homologation Reactions.
Arranged alphabetically by name reactions, the listing provides:Description of the reactionHistorical perspectiveA mechanism for the reactionVariations and improvements on the reactionSynthetic utilities of the reactionExperimental detailsReferences to the current primary literature
Armed with this invaluable resource, both students and professionals will have at their fingertips a comprehensive guide to important mechanisms and phenomena in homologation.

Spis treści:
Foreword.
Preface.
Contributing Authors.
Chapter 1: Rearrangements.
Section 1.1 Concerted rearrangement.
Section 1.2 Cationic rearrangement.
Section 1.3 Anionic rearrangement.
Chapter 2: Asymmetric CC bond formation.
2.1 Evans aldol reaction.
2.2 Hajos–Wiechert reaction.
2.3 Keck stereoselective allylation.
2.4 Roush allylboronation.
Chapter 3: Miscellaneous homologation reactions.
3.1 Bamford–Stevens reaction.
3.2 Mannich reaction.
3.3 Mitsunobu reaction.
3.4 Parham cyclization.
3.5 Passerini reacti on.
3.6 Ugi reaction.
Appendixes.
Appendix 1, Table of Contents for Volume 1: Name Reactions in Heterocyclic Chemistry.
Appendix 2, Table of Contents for Volume 2: Name Reactions for Functional Group Transformations.
Appendix 3, Table of Contents for Volume 3: Name Reactions for Homologations–I.
Appendix 4, Table of Contents for Volume 5: Name Reactions for Ring Formations.
Appendix 5, Table of Contents for Volume 6: Name Reactions in Heterocyclic Chemistry–II.
Subject index.

Nota biograficzna:
Jie Jack Li is a chemist at Bristol–Myers Squibb Company. He received his BS from Nanjing University and his PhD in organic chemistry at Indiana University. Dr. Li completed a postdoctoral fellowship at MIT. He is coauthor of various books, including Name Reactions in Heterocyclic Chemistry, Contemporary Drug Synthesis, Name Reactions for Functional Group Transformations, Name Reactions for Homologations, Parts I and II, Name Reactions on Ring Formations, and The Art of Drug Synthesis, all published by Wiley.

Okładka tylna:
"A valuable addition to the literature by any measure and surely will prove its merit in years to come. The new knowledge that arises with its help will be impressive and of great benefit to humankind."
—From the Foreword by E. J. Corey, Nobel Prize Laureate
An invaluable guide to name reactions and reagents for homologations
Name Reactions for Homologations, Part II of Wiley′s Comprehensive Name Reactions series comprises a comprehensive treatise on name reactions for homologations. With contributions from world–recognized authorities in the field, this reference offers an up–to–date, concise compilation of the most commonly used and widely known name reactions and reagents. Part II discusses Rearrangements, Asymmetric C–C Bond Formation, and Miscellaneou s Homologation Reactions.
Arranged alphabetically by name reactions, the listing provides:Description of the reactionHistorical perspectiveA mechanism for the reactionVariations and improvements on the reactionSynthetic utilities of the reactionExperimental detailsReferences to the current primary literature
Armed with this invaluable resource, both students and professionals will have at their fingertips a comprehensive guide to important mechanisms and phenomena in homologation.