E-Book, Englisch, Band Volume 1992, 485 Seiten, Web PDF
Weintraub Annual Reports in Organic Synthesis 1992
1. Auflage 2013
ISBN: 978-1-4832-9332-5
Verlag: Elsevier Science & Techn.
Format: PDF
Kopierschutz: 1 - PDF Watermark
1992
E-Book, Englisch, Band Volume 1992, 485 Seiten, Web PDF
Reihe: Annual Reports in Organic Synthesis
ISBN: 978-1-4832-9332-5
Verlag: Elsevier Science & Techn.
Format: PDF
Kopierschutz: 1 - PDF Watermark
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.'
Autoren/Hrsg.
Weitere Infos & Material
1;Front Cover;1
2;Annual Reports in Organic Synthesis –1992;4
3;Copyright Page;5
4;Table of Contents;6
5;Preface;10
6;Journals Abstracted;13
7;Glossary of Abbreviations;14
8;CHAPTER I. CARBON-CARBON BOND FORMING REACTIONS;18
8.1;A. Carbon-Carbon Single Bonds (see also: I.E., I.F., LG., I.H.);18
8.2;B. Carbon-Carbon Double Bonds (See also: I.E.I);94
8.3;C Carbon-Carbon Triple Bonds;124
8.4;D. Cyclopropanations;128
8.5;E. Thermal and Photochemical Reactions;134
8.6;F. Aromatic Substitutions Forming a New Carbon-Carbon Bond;166
8.7;G. Synthesis via Organometallics;187
8.8;H. Rearrangements;200
9;CHAPTER II. OXIDATIONS;211
9.1;A. C-O Oxidations (see also:III.F.l);211
9.2;B. C-H Oxidations;214
9.3;C C-N Oxidations;222
9.4;D. Amine Oxidations;223
9.5;E. Sulfur Oxidations;224
9.6;F. Oxidative Additions to C-C Multiple Bonds;225
9.7;G. Phenol-Quinone Oxidation;231
9.8;H. Dehydrogenation;234
10;CHAPTER III. REDUCTIONS;236
10.1;A. C=0 Reductions (see also III.F.l);236
10.2;B. C-N Multiple Bond Reductions;243
10.3;C Reduction of Sulfur Compounds;245
10.4;D. N-O Reductions;246
10.5;E. C-C Multiple Bond Reductions;248
10.6;F. Hetero Bond Reductions;253
10.7;G. Reductive Cleavages;260
10.8;H. Reduction of Azides;262
10.9;I. Reductive Cyclizations;264
10.10;J. Other Reductions;264
11;CHAPTER IV. SYNTHESIS OF HETEROCYCLES;266
11.1;A. Oxiranes, Aziridines, and Thiiranes;266
11.2;B Oxetanes, Azetidines, and Thietanes;268
11.3;C Lactams;269
11.4;D. Lactones;281
11.5;E. Furans and Thiophenes;290
11.6;F. Pyrroles, Indoles, etc;299
11.7;G. Pyridines, Quinolines, etc;309
11.8;H. Pyrans, Pyrones, and Sulfur Analogues;316
11.9;I. Other Heterocycles with One Heteroatom;323
11.10;J. Heterocycles with a Bridgehead Heteroatom;325
11.11;K. Heterocycles with Two or More Heteroatoms;329
11.12;L. Other Heterocyles;355
11.13;M. Reviews;358
12;CHAPTER V.PROTECTING GROUPS;363
12.1;A. Hydroxyl Protecting Groups;363
12.2;B. Amine Protecting Groups;370
12.3;C Carboxyl Protecting Groups;373
12.4;D. Protecting Groups for Aldehydes and Ketones;374
12.5;E. Amino Acid Protection;377
12.6;F. Other Protecting Groups;379
13;CHAPTER VI. USEFUL SYNTHETIC PREPARATIONS;382
13.1;A. Functional Group Preparations;382
13.2;B. Additions to Alkenes and Alkynes;423
13.3;C. Nucleotides, etc;425
13.4;D. Phosphorus, Selenium and Tellurium Compounds;426
13.5;E. Silicon Compounds;429
13.6;F. Sulfur Compounds;431
13.7;G. Tin Compounds;435
14;CHAPTER VII. REVIEWS;437
14.1;A. Techniques;437
14.2;B. Asymmetric Synthesis and Molecular Recognition;440
14.3;C Reactions;443
14.4;D. Reactive Intermediates;447
14.5;E. Organo-metallics and -metalloids;452
14.6;F. Halogen.Compounds and Halogenation (see also: VI.A.3.);460
14.7;G. Natural Products;461
14.8;H. Others (see also: IV.M.);467
15;AUTHOR INDEX;476
