O'Donnell / Weiss MD Annual Reports in Organic Synthesis-1983

Annual Reports in Organic Synthesis
1. Auflage 2013
ISBN: 978-1-4831-4116-9
Verlag: Elsevier Science & Techn.
Format: PDF
Kopierschutz: 1 - PDF Watermark

E-Book, Englisch, 508 Seiten, Web PDF

Annual Reports in Organic Synthesis-1983 presents an annual review of synthetically useful information that would prove beneficial to nearly all organic chemists, both specialist and nonspecialist in synthesis. It should help relieve some of the information storage burden of the specialist and should aid the nonspecialist who is seeking help with a specific problem to become rapidly aware of recent synthetic advances. In producing this volume the editors abstracted 47 primary chemistry journals, selecting useful synthetic advances. All reactions and methods which are new, synthetically useful, and reasonably general are included. Each entry is comprised primarily of structures accompanied by very few comments. The purpose of this is to aid the reader in rapidly scanning the book. Chapters I-III are organized by reaction type and constitute the major part of the book. Chapter IV deals with methods of synthesizing heterocyclic systems. Chapter V covers the use of new protecting groups. Chapter VI is divided into three main parts and covers those synthetically useful transformations that do not fit easily into the first three chapters. The first part deals only with functional group synthesis. The second part covers ring expansion and contraction, and the third part involves useful multistep sequences.

Autoren/Hrsg.

O'Donnell, Martin J.

Weiss MD, Mph

Inhaltsverzeichnis

1;Front Cover
;1
2;Annual Reports in Organic Synthesis—1983;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, I.G).;16
8.2;B. Carbon-Carbon Doub le Bonds (see also: I.E.I, III.G, III.G, VI.A.I6).;122
8.3;C. Carbon-Carbon Trip le Bonds (see also: VI.A. 16).;152
8.4;D. Cyclopropanations;156
8.5;E. Thermal Reactions;168
8.6;F. Aromatic Substitutions Forming a New Carbon-Carbon Bond;202
8.7;G. Synthes is via Organometallics;234
9;CHAPTER II. OXIDATIONS;245
9.1;A. C-O Oxidations;245
9.2;B. C-H Oxidations;251
9.3;C. C-N Oxidations;266
9.4;D. Amine Oxidations;270
9.5;E.-2 Sulfur Oxidations;272
9.6;F. Oxidative Additions to C-C Multiple Bonds;275
9.7;G. Phenol -+ Quinone Oxidation;280
9.8;H. Oxidative Cleavages;284
9.9;I. Photosensitized Oxygenations;287
9.10;J. Dehydrogenation;288
9.11;K. Other Oxidations and Reviews;289
10;CHAPTER III. REDUCTIONS;291
10.1;A. C = O Reductions (see also: III.F. 1);291
10.2;B. C-N Multiple Bond Reductions;297
10.3;C. Reduction of Sulfur Compounds;299
10.4;D. N-0 Reductions;299
10.5;E. C-C Multiple Bond Reductions;301
10.6;G. Reductive Eliminations;319
10.7;H. Reductive Cleavages;321
10.8;I. Hydroboration (reduction only);324
10.9;J. Other Reductions and Reviews;324
11;CHAPTER IV. SYNTHESIS OF HETEROCYCLES;327
11.1;A. Aziridines;327
11.2;B. Furans, etc;328
11.3;C. Indoles;333
11.4;D. Lactams;335
11.5;E. Lactones;345
11.6;F. Pyridines, Quinolines, etc;355
11.7;G. Pyrroles, etc;358
11.8;H. Other Heterocycles with One Heteroatom;361
11.9;I. Heterocycles with Two or More Heteroatoms;365
11.10;J. General Reviews;379
12;CHAPTER V. PROTECTING GROUPS;381
12.1;A. Hydroxyl (see also: VI.A. 10, VI.A. 11);381
12.2;B. Amine (see also: VI.A.4);387
12.3;C. Sulfhydryl (see also: VI.A. 19);394
12.4;D. Carboxyl (see also: VI.A.4, VI.A. 10);395
12.5;E. Ketone, Aldehyde (see also: VI.A. 18);397
12.6;F. Phosphate;401
12.7;G. Pi Bond;402
12.8;H. Miscellaneous Protecting Groups;403
13;CHAPTER VI. USEFUL SYNTHETIC PREPARATIONS;405
13.1;A. Functional Group Preparations;405
13.2;B. Ring Enlargement and Contraction;460
13.3;C. Multistep Transformations;464
14;CHAPTER VII. MISCELLANEOUS REVIEWS;462
15;AUTHOR INDEX;474