Scriven / Turnbull Annual Reports in Organic Synthesis - 1986

1. Auflage 2013
ISBN: 978-1-4831-0403-4
Verlag: Elsevier Science & Techn.
Format: PDF
Kopierschutz: 1 - PDF Watermark

E-Book, Englisch, 470 Seiten, Web PDF

Annual Reports in Organic Synthesis - 1986 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.

Scriven, Eric F. V.

Turnbull, Kenneth

Inhaltsverzeichnis

1;Front Cover;1
2;Annual Reports in Organic Synthesis—1986;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;16
8.2;B. Carbon-Carbon Double Bonds;95
8.3;C. Carbon-Carbon Triple Bond;136
8.4;D. Cyclopropanations ;143
8.5;E. Thermal Reactions;152
8.6;F. Aromatic Substitutions Forming a New Carbon-Carbon Bond;181
8.7;G. Synthesis via Organometallics;202
8.8;H. Rearrangements;218
9;CHAPTER
II. OXIDATIONS;230
9.1;A. C-O Oxidations ;230
9.2;B. C-H Oxidations;234
9.3;C. C-N Oxidations ;244
9.4;D. Amine Oxidations .;246
9.5;E. Sulfur Oxidations ;247
9.6;F. Oxidative Additions to C-C Multiple Bonds;249
9.7;G. Phenol-Quinone Oxidation;255
9.8;H. Oxidative Cleavages;255
9.9;I. Dehydrogenation;256
9.10;J. Other Oxidations and Reviews ;256
10;CHAPTER
III. REDUCTIONS ;260
10.1;A. C=O Reductions;260
10.2;B. C-N Multiple Bond Reductions ;269
10.3;C. Reduction of Sulfur Compounds;271
10.4;D. N-O Reductions;272
10.5;E. C-C Multiple Bond Reductions;275
10.6;F. Hydrogenolysis of Hetero Bonds;280
10.7;G. Reductive Cleavages ;289
10.8;H. Reduction of Azides ;290
10.9;I. Reviews;291
11;CHAPTER
IV. SYNTHESIS OF HETEROCYCLES;294
11.1;A. Oxiranes;294
11.2;B. Azirines and Aziridines;296
11.3;C. Oxetanes;297
11.4;D. Lactams ;298
11.5;E. Lactones;306
11.6;F. Furans, Thiophenes, etc;318
11.7;G. Pyrroles, Indoles, etc;323
11.8;H. Pyridines and Quinolines ;329
11.9;I. Pyrans, Pyrones, etc;333
11.10;J. Other Heterocycles with One Heteroatom ;337
11.11;K. Heterocycles with a Bridgehead Heteroatom;338
11.12;L. Heterocycles with Two or More Heteroatoms ;340
11.13;M. Other Heterocycles ;363
11.14;N. General Heterocyclic Reviews ;366
12;CHAPTER
V. PROTECTING GROUPS;371
12.1;A. Hydroxyl Protecting Groups ;371
12.2;B. Amine Protecting Groups;376
12.3;C. Sulfhydryl Protection ;380
12.4;D. Carboxyl Protecting Groups ;380
12.5;E. Protecting Groups for Aldehydes and Ketones;381
12.6;F. Phosphate Protecting Groups;384
12.7;G. Nitrone Protection;387
12.8;H. Review ;387
13;CHAPTER
VI. USEFUL SYNTHETIC PREPARATIONS;388
13.1;A. Functional Group Preparations ;388
13.2;B. Sulfur Compounds ;420
13.3;C. Phosphorus Compounds;428
13.4;D. Se Compounds ;429
13.5;E. Nucleotides, etc;431
14;CHAPTER
VII. OTHER REVIEWS ;433
14.1;A. Techniques;433
14.2;B. Asymmetric Synthesis;435
14.3;C. Reactions;436
14.4;D. Reactive Intermediates ;438
14.5;E. Organo-metallics and -metalloids;439
14.6;F. Halogen-Compounds and Halogenation ;443
14.7;G. Natural Products;444
14.8;H. Others ;448
15;AUTHOR INDEX;452