E-Book, Englisch, 546 Seiten, Web PDF
Weintraub Annual Reports in Organic Synthesis-1993
1. Auflage 2013
ISBN: 978-0-08-091623-1
Verlag: Elsevier Science & Techn.
Format: PDF
Kopierschutz: 1 - PDF Watermark
1993
E-Book, Englisch, 546 Seiten, Web PDF
ISBN: 978-0-08-091623-1
Verlag: Elsevier Science & Techn.
Format: PDF
Kopierschutz: 1 - PDF Watermark
This handy reference tool is an organized annual review of synthetically useful information. It abstracts synthetic reactions from the major chemistry journals of the past year and includes all reactions and methodsthat are new and reasonably general. The reactions are presented in a convenient pictorial format designed for rapid visual retrieval of information. The Journal of the American Chemical Society has aptly described this publication as an'aid to the harassed organic chemist who cannot keep up with the never-diminishing stream of new primary literature'and hails it'an outstandingly good buy.' - Clearly illustrated structures of compounds in every feasible syntheticpathway - A general review of structure/activity information for each synthetic compound - Extensive reference information provided for additional publications available for each reactiondiscussed
Autoren/Hrsg.
Weitere Infos & Material
1;Front Cover;1
2;Annual Reports in Organic Synthesis — 1993;4
3;Copyright Page;5
4;Table of Contents;6
5;PREFACE;10
6;JOURNALS ABSTRACTED;14
7;GLOSSARY OF ABBREVIATIONS;16
8;CHAPTER I. CARBON-CARBON BOND FORMING REACTIONS;20
8.1;A. Carbon-Carbon Single Bonds (see also: I.E., I.F., I.G., I.H.);20
8.2;B. Carbon-Carbon Double Bonds (See also: I.E.1);91
8.3;C. Carbon-Carbon Triple Bonds;114
8.4;D. Cyclopropanations;118
8.5;E. Thermal and Photochemical Reactions;124
8.6;F. Aromatic Substitutions Forming a New Carbon-Carbon Bond..;151
8.7;G. Synthesis via Organometallics;168
8.8;H. Rearrangements;192
9;CHAPTER II. OXIDATIONS;227
9.1;A. C-0 Oxidations (see also:III.F.1);227
9.2;B. C-H Oxidations;232
9.3;C. C-N Oxidations;246
9.4;D. Amine Oxidations;247
9.5;E. Sulfur Oxidations;249
9.6;F. Oxidative Additions to C-C Multiple Bonds;252
9.7;G. Phenol-Quinone Oxidation;266
9.8;H. Dehydrogenation;270
10;CHAPTER III. REDUCTIONS;273
10.1;A. C=O Reductions (see also III.F.1);273
10.2;B. C-N Multiple Bond Reductions;289
10.3;C Reduction of Sulfur Compounds;293
10.4;D. N-O Reductions;294
10.5;E. C-C Multiple Bond Reductions;295
10.6;F. Hetero Bond Reductions;303
10.7;G. Reductive Cleavages;314
10.8;H. Reduction of Azides;317
10.9;I. Reductive Cyclizations;317
10.10;J. Other Reductions;318
11;CHAPTER IV. SYNTHESIS OF HETEROCYCLES;321
11.1;A. Oxiranes, Aziridines, and Thiiranes;321
11.2;B. Oxetanes, Azetidines, and Thietanes;324
11.3;C. Lactams;326
11.4;D. Lactones;337
11.5;E. Furans and Thiophenes;346
11.6;F. Pyrroles, Indoles, etc;355
11.7;G. Pyridines, Quinolines, etc;366
11.8;H. Pyrans, Pyrones, and Sulfur Analogues;375
11.9;I. Other Heterocycles with One Heteroatom;381
11.10;J. Heterocycles with a Bridgehead Heteroatom;383
11.11;K. Heterocycles with Two or More Heteroatoms;389
11.12;L. Other Heterocycles;418
11.13;M. Reviews;421
12;CHAPTER V. PROTECTING GROUPS;429
12.1;A. Hydroxyl Protecting Groups;429
12.2;B. Amine Protecting Groups;433
12.3;C. Carboxyl Protecting Groups;435
12.4;D. Protecting Groups for Aldehydes and Ketones;436
12.5;E. Amino Acid Protection;438
12.6;F. Other Protecting Groups;440
13;CHAPTER VI. USEFUL SYNTHETIC PREPARATIONS;442
13.1;A. Functional Group Preparations;442
13.2;B. Additions to Alkenes and Alkynes;482
13.3;C. Nucleotides, etc;484
13.4;D. Phosphorus, Selenium and Tellurium Compounds;486
13.5;E. Silicon Compounds;488
13.6;F. Sulfur Compounds;490
13.7;G. Tin Compounds;495
14;CHAPTER VII. REVIEWS;497
14.1;A. Techniques;497
14.2;B. Asymmetric Synthesis and Molecular Recognition;500
14.3;C. Reactions;506
14.4;D. Reactive Intermediates;510
14.5;E. Organo-metallics and -metalloids;512
14.6;F. Halogen.Compounds and Halogenation (see also: VI.A.3.);519
14.7;G. Natural Products;521
14.8;H. Others (see also: IV.M.);528
15;AUTHOR INDEX;538
