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Name reactions for homologations / edited by Jie Jack Li ; foreword by E. J. Corey.
Holman Biotech Commons QD262 .N363 2009 pts.1-2
Available
- Format:
- Book
- Language:
- English
- Subjects (All):
- Organic compounds--Synthesis.
- Organic compounds.
- Chemical reactions.
- Chemical tests and reagents.
- Physical Description:
- 2 volumes : illustrations ; 25 cm
- Place of Publication:
- Hoboken, N.J. : Wiley, [2009]
- Summary:
- An Invaluable Guide to Name Reactions and Reagents for Homologation
- 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 reaction
- Historical perspective
- A mechanism for the reaction
- Variations and improvements on the reaction
- Synthetic utilities of the reaction
- Experimental details
- References 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.
- Contents:
- Chapter 1 Rearrangements 1
- Section 1.1 Concerted rearrangement 2
- 1.1.1 Alder ene reaction 2
- 1.1.2 Claisen and related rearrangements 33
- 1.1.3 Cope and related rearrangements 88
- 1.1.4 Curtius rearrangement 136
- 1.1.5 Hofmann rearrangement 164
- 1.1.6 Lossen rearrangement 200
- 1.1.7 Overman rearrangement 210
- 1.1.8 [1,2]-Wittig rearrangement 226
- 1.1.9 [2,3]-Wittig rearrangement 241
- 1.1.10 Wolff rearrangement 257
- Section 1.2 Cationic rearrangement 274
- 1.2.1 Beckmann rearrangement 274
- 1.2.2 Demjanov rearrangement 293
- 1.2.3 Meyer-Schuster rearrangement 305
- 1.2.4 Pinacol rearrangement 319
- 1.2.5 Pummerer rearrangement 334
- 1.2.6 Schmidt rearrangement 353
- 1.2.7 Wagner-Meerwein rearrangement 373
- Section 1.3 Anionic rearrangement 395
- 1.3.1 Benzilic acid rearrangement 395
- 1.3.2 Brook rearrangement 406
- 1.3.3 Favorskii rearrangement 438
- 1.3.4 Grob fragmentation 452
- 1.3.5 Neber rearrangement 464
- 1.3.6 Payne rearrangement 474
- 1.3.7 Smiles rearrangement 489
- 1.3.8 Stevens rearrangement 516
- Chapter 2 Asymmetric C-C bond formation 531
- 2.1 Evans aldol reaction 532
- 2.2 Hajos-Wiechert reaction 554
- 2.3 Keck stereoselective allylation 583
- 2.4 Roush allylboronation 613
- Chapter 3 Miscellaneous homologation reactions 641
- 3.1 Bamford-Stevens reaction 642
- 3.2 Mannich reaction 653
- 3.3 Mitsunobu reaction 671
- 3.4 Parham cyclization 749
- 3.5 Passerini reaction 765
- 3.6 Ugi reaction 786.
- Notes:
- Includes bibliographical references and index.
- Local Notes:
- Acquired for the Penn Libraries with assistance from the Alumni and Friends Memorial Book Fund.
- ISBN:
- 9780470467213
- 0470467215
- 9780470085073
- 047008507X
- 9780470464984
- 0470464984
- OCLC:
- 297222809
- Publisher Number:
- 99935859110
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