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Annual reports in organic synthesis. 1994 /

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 pict...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Weintraub, Philip M. (Editor )
Formato: Electrónico eBook
Idioma:Inglés
Publicado: San Diego : Academic Press, 1994.
Colección:Annual Reports in Organic Synthesis.
Temas:
Acceso en línea:Texto completo

MARC

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245 0 0 |a Annual reports in organic synthesis.  |n 1994 /  |c edited by Philip M. Weintraub ... [and more]. 
264 1 |a San Diego :  |b Academic Press,  |c 1994. 
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490 1 |a Annual Reports in Organic Synthesis ;  |v v. 94 
588 0 |a Online resource; title from PDF title page (ScienceDirect, viewed November 4, 2014). 
505 0 |a Front Cover; Annual Reports in Organic Synthesis -- 1994; Copyright Page; Table of Contents; PREFACE; JOURNALS ABSTRACTED; GLOSSARY OF ABBREVIATIONS; CHAPTER I. CARBON-CARBON BOND FORMING REACTIONS; A. Carbon -- Carbon Single Bonds (see also: I.E., I.F., I.G., I.H.); B. Carbon-Carbon Double Bonds (See also: I.E.I); C. Carbon-Carbon Triple Bonds; D. Cyclopropanations; E. Thermal and Photochemical Reactions; F. Aromatic Substitutions Forming a New Carbon-Carbon Bond.; G. Synthesis via Organometallics; H. Rearrangements; CHAPTER II. OXIDATIONS; A. Alcohol ₂!Ketone. Aldehyde; B. C-H Oxidations. 
505 8 |a C. C-N OxidationsD. Amine Oxidations; E. Sulfur Oxidations; F. Oxidative Additions to C-C Multiple Bonds; G. Phenol₂!uinone Oxidation; H. Dehydrogenation; I. Miscellaneous Oxidations; CHAPTER III. REDUCTIONS; A. C=0 Reductions (see also III. F.l); B. C-N Multiple Bond Reductions; E. C-C Multiple Bond Reductions; F. Hetero Bond Reductions; G. Reductive Cleavages; H. Reduction of Azides; CHAPTER IV. SYNTHESIS OF HETEROCYCLES; A. Oxiranes, Aziridines, and Thiiranes; B. Oxetanes, Azetidines, and Thietanes; C. Lactams; D. Lactones; E. Furans and Thiophenes; F. Pyrroles, Indoles, etc. 
505 8 |a G. Pyridines, Quinolines, etcH. Pyrans, Pyrones, and Sulfur Analogues; I. Other Heterocycles with One Heteroatom; J. Heterocycles with a Bridgehead Heteroatom; K. Heterocycles with Two or More Heteroatoms; L. Other Heterocyles; M. Reviews; CHAPTER V. PROTECTING GROUPS; A. Hydroxyl Protecting Groups; B. Amine Protecting Groups; C. Carboxyl Protecting Groups; D. Protecting Groups for Aldehydes and Ketones; E. Amino Acid Protection; F. Other Protecting Groups; CHAPTER VI. USEFUL SYNTHETIC PREPARATIONS; A. Functional Group Preparations; B. Additions to Alkenes and Alkynes; C. Nucleotides, etc. 
505 8 |a D. Phosphorus, Selenium and Tellurium CompoundsE. Silicon Compounds; F. Sulfur Compounds; G. Tin Compounds; CHAPTER VII. REVIEWS; A. Techniques; B. Asymmetric Synthesis and Molecular Recognition; C. Reactions; D. Reactive Intermediates; E. Organo-metallics and -metalloids; F. Halogen Compounds and Halogenation (see also: VI. A.11.); G. Natural Products; H. Others (see also: IV. M.); AUTHOR INDEX. 
520 |a 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 
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650 7 |a Organic compounds  |x Synthesis  |2 fast  |0 (OCoLC)fst01047668 
700 1 |a Weintraub, Philip M.,  |e editor. 
776 0 8 |i Print version:  |a Weintraub, Philip M.  |t Annual Reports in Organic Synthesis 1994.  |d Burlington : Elsevier Science, �2013  |z 9780120408245 
830 0 |a Annual Reports in Organic Synthesis. 
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