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Organic Syntheses Based on Name Reactions
ID: 174127
A. Hassner
Organic Syntheses Based on Named Reactions 3 rd edition is an indispensable reference companion for students. Effectively and more specifically, this product is a reference to the product. Each entry is carefully conducised to the best of the future.
Building on Hassner & Stumer's highly regarded 2 nd edition and publishing at the time of proliferation. covered to over 700.
It summarizes the reaction types' various laboratory uses, including around 3,400 references to other sources; a functional group transformation index.
[Latter The The chem chem chem chem The synthetic chem The The The The] latter The chem chem chem chem proved chem chem chem chem chem chem chem chem proved. Chem chem The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The The
Due to its comprehensive coverage, superb organization, and quality of references, this long-awaited book belongs to the shelf of every organic chemist.
* Handy reference guide that explains over common and uncommon chemists
* Provides key data on each and other machinery, including the experimental details
* Extensive and multiple indexes
Name reactions; Names index; Reagents index; Reactions index; Functional Group Transformations index.
Sample Name Reactions: Appel, Halogenation Reagent; Bailey, Crisscross Cycloaddition; Barluenga, Iodination; Barton-McCrombie, Deoxygenation; Bergman, Cycloaromatization; Brandi-Guarna, Rearrangement; Buchwald, Heterocyclization; Chiatgilialoglu, Reducing Agent; G. Enders, Heterocycle Synthesis;
Grubbs, Olefin Metathesis; Jacobsen, Asymmetric Epoxidation; Kagan-Modena, Asymemetric Oxidation; Katritzky, Amine Displacement; Kawase, N-Acyl Rearrangement; Knochel, Zinc Vinyl Coupling; Kulinkovich, Hydroxycyclopropanation; Nicolaou, Oxidations; O'Donnell, Aminoacid Synthesis; Saegusa, Enone Synthesis; Shibasaki, Catalytic Nitrogenation; Yamamoto, Chiral Transfer
174127
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A. Hassner