E-Book, Englisch, 488 Seiten, Web PDF
Scriven / Turnbull Annual Reports in Organic Synthesis - 1987
1. Auflage 2013
ISBN: 978-1-4831-0402-7
Verlag: Elsevier Science & Techn.
Format: PDF
Kopierschutz: 1 - PDF Watermark
E-Book, Englisch, 488 Seiten, Web PDF
ISBN: 978-1-4831-0402-7
Verlag: Elsevier Science & Techn.
Format: PDF
Kopierschutz: 1 - PDF Watermark
Annual Reports in Organic Synthesis - 1987 presents a collection of 49 abstracted chemistry journals that cover organic synthesis. The book is comprised of eight chapters that cover different aspects of organic synthesis, such as reaction types and methods. The first three chapters tackle carbon-carbon bond forming reactions, oxidations, and reductions. Chapter IV discusses synthesis of heterocycles, and Chapter V covers the use of protecting groups. Chapter VI talks about useful synthetic preparations. The last two chapters cover the miscellaneous reactions and reviews. The text will be useful to biochemists and other researchers who deal with organic synthesis.
Autoren/Hrsg.
Weitere Infos & Material
1;Front Cover;1
2;Annual Reports in Organic Synthesis—1987;4
3;Copyright Page;5
4;Table of Contents;6
5;PREFACE;10
6;JOURNALS ABSTRACTED;12
7;GLOSSARY OF ABBREVIATIONS;14
8;CHAPTER I. CARBON-CARBON BOND FORMING REACTIONS;16
8.1;A. Carbon-Carbon Single Bonds (see also: I.E., I.F., LG., I.H.);16
8.2;B. Carbon-Carbon Double Bonds (see also: I.E.I, III.G);103
8.3;C Carbon-Carbon Triple Bonds;148
8.4;D. Cyclopropanations;154
8.5;E. Thermal and Photochemical Reactions;163
8.6;F. Aromatic Substitutions Forming a New Carbon-Carbon Bond;195
8.7;G. Synthesis via Organometallics;220
8.8;H. Rearrangements;235
9;CHAPTER II. OXIDATIONS;249
9.1;A. C–O Oxidations;249
9.2;B. C–H Oxidations;253
9.3;C C–N Oxidations;260
9.4;D. Amine Oxidations;261
9.5;E. Sulfur Oxidations;262
9.6;F. Phosphorus and Selenium Oxidation;263
9.7;G. Oxidative Additions to C–C Multiple Bonds;264
9.8;H. Phenol-Quinone Oxidation;270
9.9;I. Dehydrogenation;271
9.10;J. Other Oxidations;271
9.11;K. Reviews;272
10;CHAPTER III. REDUCTIONS;274
10.1;A. C = 0 Reductions (see also: III.F.l);274
10.2;B. C–N Multiple Bond Reductions;281
10.3;C Reduction of Sulfur Compounds;283
10.4;D. N–O Reductions;284
10.5;E. C–C Multiple Bond Reductions;286
10.6;F. Hetero Bond Reductions;293
10.7;G. Reductive Cleavages;299
10.8;H. Reduction of Azides;303
10.9;I. Reviews;304
11;CHAPTER IV. SYNTHESIS OF HETEROCYCLES;306
11.1;A. Oxiranes and Aziridines;306
11.2;B. Oxetanes;307
11.3;C. Lactams;308
11.4;D. Lactones;315
11.5;E. Furans, Thiophenes, Etc;327
11.6;F. Pyrroles, Indoles, Etc;334
11.7;G. Pyridines, Quinolines, Etc;338
11.8;H. Pyrans, Pyrones, Etc;341
11.9;I. Other Heterocycles with One Heteroatom;345
11.10;J. Heterocycles with a Bridgehead Heteroatom;346
11.11;K. Heterocycles with Two or More Heteroatoms;347
11.12;L. Other Heterocycles;362
11.13;M. Reviews;364
12;CHAPTER V. PROTECTING GROUPS;374
12.1;A. Hydroxyl Protecting Groups(see also: VI.A.9);374
12.2;B. Amine Protecting Groups (see also: VI.A.4);380
12.3;C Carboxyl Protecting Groups (see also: VI.A.4);383
12.4;D. Protecting Groups for Aldehydes and Ketones;384
12.5;E. Amino Acid Protection;386
12.6;F Oxime Protection;389
12.7;G. Reviews;390
13;CHAPTER VI. USEFUL SYNTHETIC PREPARATIONS;391
13.1;A. Functional Group Preparations;391
13.2;B. Sulfur Compounds;429
13.3;C Phosphorus and Tellurium Compounds;435
13.4;D. Nucleotides, etc;438
14;CHAPTER VII. OTHER REVIEWS;442
14.1;A. Techniques;442
14.2;B. Asymmetric Synthesis;444
14.3;C Reactions;447
14.4;D. Reactive Intermediates;450
14.5;E. Organo-metallics and -metalloids;453
14.6;F. Halogen-Compounds and Halogenation;459
14.7;G. Natural Products;461
14.8;H. Others;464
15;AUTHOR INDEX;470
