In this sixth edition of Jack Jie Li's seminal "Name Reactions", the author has added three or more synthetic applications of name reactions to reflect the recent advances in organic chemistry. As in previous editions, each reaction is delineated by its detailed step-by-step, electron-pushing mechanism and supplemented with the original and the latest references, especially from review articles. This book is not only an indispensable resource for advanced undergraduate and graduate students for learning and preparing exams, but is also a good reference book for all organic chemists in both industry and academia.
Unlike other books on name reactions in organic chemistry, Name Reactions, A Collection of Detailed Reaction Mechanisms and Synthetic Applications focuses on the reaction mechanisms. It covers over 300 classical as well as contemporary name reactions.
Auflage
Sprache
Verlagsort
Verlagsgruppe
Springer International Publishing
Zielgruppe
Editions-Typ
Illustrationen
524
1136 s/w Abbildungen, 524 farbige Abbildungen
XXII, 601 p. 1660 illus., 524 illus. in color.
Maße
Höhe: 241 mm
Breite: 160 mm
Dicke: 37 mm
Gewicht
ISBN-13
978-3-030-50864-7 (9783030508647)
DOI
10.1007/978-3-030-50865-4
Schweitzer Klassifikation
Jie Jack Li
Before joining ChemPartner as Vice President of Discovery Chemistry, Dr. Jie Jack Li practiced medicinal chemistry for over twenty years at Pfizer, BMS, and Revolution Medicines, respectively, with a four-year sojourn at the University of San Francisco as an Associate Professor, teaching medicinal and organic chemistry. He has published thirty books in organic chemistry, medicinal chemistry, and history of drug discovery. Chief among them are Drug Discovery: Practices, Processes, and Perspectives and Name Reactions, now in the sixth edition.
From the Contents: Alder ene reaction.- Baran Reagents.- Bargellini Reaction.- Barton-Zard reaction.- Beirut reaction.- Boyland-Sims oxidation.- Cattallani Reaction.- Danheiser annulation.- Kolbe-Schmitt Reaction.- Larock Indole Synthesis.- Li A3 Reaction.- McMillan Catalyst.- Meth-Cohn Quinoline Synthesis.- Sanford Reaction.- Shi-White Reagent.- Stevens Rearrangement.- Stork-Danheiser alkylation.- Weinreb Amide.- Yu C-H Activation.- Zaitsev Elimination.- Zinin Benzidine Rearrangement (Semidine Rearrangement).
