O'Donnell / Weiss MD Annual Reports in Organic Synthesis-1984

Annual Reports in Organic Synthesis
1. Auflage 2013
ISBN: 978-1-4831-4115-2
Verlag: Elsevier Science & Techn.
Format: PDF
Kopierschutz: 1 - PDF Watermark

E-Book, Englisch, 514 Seiten, Web PDF

Annual Reports in Organic Synthesis-1984 is a bibliography of papers on organic synthesis from primary chemistry journals. Topics covered range from carbon-carbon bond forming reactions to oxidations, reductions, synthesis of heterocycles, and synthetic preparations. This book consists of seven chapters and begins with a list of papers on carbon-carbon bond forming reactions, including carbon-carbon single, double, and triple bonds. The chapters that follow focus on oxidations and reductions, methods of synthesizing heterocyclic systems, and the use of protecting groups. Synthetically useful transformations that do not fit easily into the first three chapters are considered next, with emphasis on functional group synthesis, ring expansion and contraction, and useful multistep transformations. The final chapter deals with miscellaneous reviews on topics ranging from cycloadditions to asymmetric catalysis, metalation, electrophilic substitutions, and pyrylium-mediated transformations of primary amino groups into other functional groups. This monograph will be of value to organic chemists, both specialist and nonspecialist in synthesis.

Autoren/Hrsg.

O'Donnell, Martin J.

Weiss MD, Mph

Inhaltsverzeichnis

1;Front Cover;1
2;Annual Reports in Organic Synthesis—1984;4
3;Copyrigh 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;I.A. Carbon-Carbon Single Bonds;16
8.2;I.B. Carbon-Carbon Double Bonds;136
8.3;I.C. Carbon-Carbon Triple Bonds;169
8.4;I.D. Cyclopropanations;173
8.5;I.E. Thermal Reactions;190
8.6;I.F, Aromatic Substitutions Forming a New Carbon-Carbon Bond;217
8.7;I.G. Synthesis via Organometallies;246
9;Chapter II. OXIDATIONS;258
9.1;II.A. C — O Oxidations;258
9.2;II.B.C — . Oxidations;264
9.3;II.C . C — . Oxidations;276
9.4;II.D . Amine Oxidations;277
9.5;II.E . Sulfur Oxidations;279
9.6;II.F . Oxidative Additions to C - C Multiple Bonds;282
9.7;II.G. Phenol Quinone Oxidation;292
9.8;II.H . Oxidative Cleavages;293
9.9;II.I. Photosensitized Oxygenations;297
9.10;II.J . Dehydrogenation;298
9.11;II.K. Other Oxidations and Reviews;300
10;Chapter III. REDUCTIONS;302
10.1;III.A. C=O Reductions;302
10.2;111... C-N Multiple Bond Reductions;310
10.3;III.C. Reductions of Sulfur Compounds;311
10.4;III.D. .—0 Reductions;313
10.5;III.E. C — C Multiple Bond Reductions;317
10.6;III.F. Hydrogenolysis of Hetero Bonds;322
10.7;III.G. Reductive Eliminations;332
10.8;III.H. Reductive Cleavages;334
10.9;III.I. Hydroboration (Reduction only);335
10.10;III.J. Other Reductions and Reviews;337
11;Chapter IV. SYNTHESIS OF HETEROCYCLES;340
11.1;IV.A. Aziridines;340
11.2;IV.B. Furans, etc.;341
11.3;I.V.C. Indoles;345
11.4;IV.D. Lactams;349
11.5;IV.E. Lactones;359
11.6;IV.F. Pyridines, Quinolines, etc.;368
11.7;IV.G. Pyrroles, etc.;370
11.8;IV.H. Other Heterocycles with One Heteroatom;373
11.9;IV.I. Heterocycles with Two or More Heteroatoms;376
11.10;IV.J. General Heterocyclic Reviews;388
12;Chapter V. PROTECTING GROUPS;390
12.1;V.A. Hydroxy1 Protecting Groups;390
12.2;V.B. Amine Protecting Groups;399
12.3;V.C. Sulfhydryl Protecting Groups;404
12.4;V.D. Carboxyl Protecting Groups;406
12.5;V.E. Protecting Groups for Ketones and Aldehydes;409
12.6;V.F. Phosphate Protecting Groups;413
12.7;V.G. Pi-Bond Protecting Groups;415
12.8;V.H. Miscellaneous Protecting Groups;415
13;Chapter VI. USEFUL SYNTHETIC PREPARATIONS;417
13.1;VI.A. Functional Group Preparations;417
13.2;VI.B.1. Ring Enlargement;467
13.3;C. Multistep Transformations;464
14;Chapter VII. MISCELLANEOUS REVIEWS;470
15;AUTHOR INDEX;480