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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
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Format:
Book
Contributor:
Li, Jie Jack.
Alumni and Friends Memorial Book Fund.
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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