Weintraub Annual Reports in Organic Synthesis 1994

1. Auflage 2013
ISBN: 978-0-08-091624-8
Verlag: Elsevier Science & Techn.
Format: PDF
Kopierschutz: 1 - PDF Watermark

E-Book, Englisch, Band Volume 94, 461 Seiten, Web PDF

Reihe: Annual Reports in Organic Synthesis

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 synthetic pathway - A general review of structure/activity information for each synthetic compound - Extensive reference information provided on additional publications available for each reaction discussed

Autoren/Hrsg.

Weintraub, Philip M.

Inhaltsverzeichnis

1;Front Cover;1
2;Annual Reports in Organic Synthesis – 1994;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;22
8.1;A. Carbon - Carbon Single Bonds (see also: I.E., I.F., I.G., I.H.);22
8.2;B. Carbon-Carbon Double Bonds (See also: I.E.I);94
8.3;C. Carbon-Carbon Triple Bonds;119
8.4;D. Cyclopropanations;123
8.5;E. Thermal and Photochemical Reactions;129
8.6;F. Aromatic Substitutions Forming a New Carbon-Carbon Bond..;158
8.7;G. Synthesis via Organometallics;175
8.8;H. Rearrangements;186
9;CHAPTER II. OXIDATIONS;205
9.1;A. Alcohol . Ketone. Aldehyde;205
9.2;B. C-H Oxidations;208
9.3;C. C-N Oxidations;216
9.4;D. Amine Oxidations;216
9.5;E. Sulfur Oxidations;217
9.6;F. Oxidative Additions to C-C Multiple Bonds;218
9.7;G. Phenol.Quinone Oxidation;228
9.8;H. Dehydrogenation;229
9.9;I. Miscellaneous Oxidations;232
10;CHAPTER III. REDUCTIONS;235
10.1;A. C=0 Reductions (see also III.F.l);235
10.2;B. C-N Multiple Bond Reductions;242
10.3;E. C-C Multiple Bond Reductions;245
10.4;F. Hetero Bond Reductions;251
10.5;G. Reductive Cleavages;259
10.6;H. Reduction of Azides;261
11;CHAPTER IV. SYNTHESIS OF HETEROCYCLES;263
11.1;A. Oxiranes, Aziridines, and Thiiranes;263
11.2;B. Oxetanes, Azetidines, and Thietanes;265
11.3;C. Lactams;266
11.4;D. Lactones;275
11.5;E. Furans and Thiophenes;283
11.6;F. Pyrroles, Indoles, etc;290
11.7;G. Pyridines, Quinolines, etc;301
11.8;H. Pyrans, Pyrones, and Sulfur Analogues;307
11.9;I. Other Heterocycles with One Heteroatom;312
11.10;J. Heterocycles with a Bridgehead Heteroatom;315
11.11;K. Heterocycles with Two or More Heteroatoms;319
11.12;L. Other Heterocyles;341
11.13;M. Reviews;343
12;CHAPTER V. PROTECTING GROUPS;349
12.1;A. Hydroxyl Protecting Groups;349
12.2;B. Amine Protecting Groups;353
12.3;C. Carboxyl Protecting Groups;355
12.4;D. Protecting Groups for Aldehydes and Ketones;357
12.5;E. Amino Acid Protection;359
12.6;F. Other Protecting Groups;361
13;CHAPTER VI. USEFUL SYNTHETIC PREPARATIONS;363
13.1;A. Functional Group Preparations;363
13.2;B. Additions to Alkenes and Alkynes;403
13.3;C. Nucleotides, etc;406
13.4;D. Phosphorus, Selenium and Tellurium Compounds;408
13.5;E. Silicon Compounds;410
13.6;F. Sulfur Compounds;412
13.7;G. Tin Compounds;416
14;CHAPTER VII. REVIEWS;418
14.1;A. Techniques;418
14.2;B. Asymmetric Synthesis and Molecular Recognition;422
14.3;C. Reactions;426
14.4;D. Reactive Intermediates;430
14.5;E. Organo-metallics and -metalloids;434
14.6;F. Halogen Compounds and Halogenation (see also: VI.A.11.);439
14.7;G. Natural Products;440
14.8;H. Others (see also: IV.M.);448
15;AUTHOR INDEX;456