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Annual Reports in Organic Synthesis (2003) : Volume 2003 - Philip M. Weintraub

Annual Reports in Organic Synthesis (2003)

Volume 2003

Paperback

Published: 1st November 2003
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The first three chapters of this latest volume are organised by reaction type. Later chapters deal with methods of synthesizing heterocyclic systems, the use of protecting groups and synthetically useful transformations. The final chapters deals with reviews and are divided by specific topics.
Clearly organised review of synthetically useful information. Emphasize on rapid visual retrieval.
Extensive use of references.
Beneficial to nearly all organic chemists, both specialists and nonspecialists in synthesis.

"This information will be useful to nearly all organic chemists, both specialists and nonspecialists in synthesis. The topics covered include carbon-carbon bond forming reactions, oxidation-reductions, synthesis of heterocycles, protecting groups, and useful synthetic preparations."
--BIOSIS
..".an aid to the harassed organic chemist who cannot keep up with the never-diminishing stream of new primary literature..."
--JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
..".an outstandingly good buy..."
--JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Prefacep. xi
List of Journals Abstractedp. xv
Glossary of Abbreviationsp. xvii
Carbon-Carbon Bond Forming Reactions
Carbon-Carbon Single Bonds (see also: I.E., I.F., I.G., I.H.)p. 1
Alkylations of Aldehydes, Ketones, and their Derivativesp. 1
Alkylations of Nitriles, Acids and Acid Derivativesp. 3
Alkylations of [beta]-Dicarbonyl, [beta]-Cyanocarbonyl Systems, and Other Active Methylene Compoundsp. 6
Alkylations of N-, P-, S-, Se & Similar Stabilized Carbanionsp. 8
Alkylations of Organometallic Reagents (see also: I.B.3., I.B.4., I.F., I.G.)p. 10
Other Alkylation Proceduresp. 13
Nucleophilic Addition to Electrophilic Carbonp. 14
1,2-Additionsp. 14
Aldol-Type 1,2 Additionsp. 14
Addition of N, P, S, Se & Similar Stabilized Carbanionsp. 21
Addition of Organometallic and Related Speciesp. 21
Other 1,2-Additionsp. 33
Conjugate Additionsp. 35
Enolate-Type Carbanionsp. 35
Organometallic and Related Reagentsp. 37
Other Conjugate Additionsp. 40
Other Carbon-Carbon Single Bond Forming Reactionsp. 42
Carbon-Carbon Double Bonds (See also: I.E.1)p. 45
Wittig-Type Olefination Reactionsp. 45
Eliminationsp. 47
Alcohols and Derivativesp. 47
Halidesp. 48
Other Eliminationsp. 48
Olefin Metathesesp. 49
Other Carbon-Carbon Double Bond Forming Reactionsp. 52
Vinylationsp. 55
Allene Forming Reactionsp. 58
Carbon-Carbon Triple Bondsp. 59
Cyclopropanationsp. 62
Carbene or Carbenoid Additions to a Multiple Bondp. 62
Other Cyclopropanationsp. 63
Thermal and Photochemical Reactionsp. 66
Cycloadditionsp. 66
Other Thermal Reactionsp. 75
Photochemical Reactionsp. 75
Aromatic Substitutions Forming a New Carbon-Carbon Bondp. 77
Friedel-Crafts Type Aromatic Substitution Reactionsp. 77
Coupling Reactions to Form an Aromatic Carbon-Aromatic Carbon Bondp. 80
Other Aromatic Substitutions and Preparationsp. 84
Synthesis via Organometallicsp. 88
Synthesis via Organoboranesp. 88
Carbonylation Reactionsp. 90
Other Syntheses via Organometallicsp. 93
Rearrangementsp. 97
Claisen, Cope and Similar Processesp. 97
Other Rearrangementsp. 100
Oxidations
C-O Oxidationsp. 104
Alcohol to Ketones, Aldehydesp. 104
Alcohols, Aldehydes to Acids, Estersp. 107
C-H Oxidationsp. 108
C-H to C-Op. 108
C-H to C-Halp. 110
C-N Oxidationsp. 110
Amine Oxidationsp. 110
Sulfur Oxidationsp. 110
Oxidative Additions to C-C Multiple Bondsp. 112
Epoxidationsp. 112
Hydroxylationsp. 114
Other Oxidative Additions to C-C Multiple Bondsp. 115
Phenol-Quinone Oxidationp. 116
Dehydrogenationsp. 116
Other Oxidationsp. 117
Reductions
C=O Reductions (see also III.F.1)p. 119
Aldehydes, Ketones to Alcoholsp. 119
Acids, Esters, Amides to Aldehydesp. 123
Acids, Esters, Amides to Alcoholsp. 123
Acids, Esters, Anhydrides to Otherp. 124
C-N Multiple Bond Reductionsp. 124
Imine Reductionsp. 124
Reduction of Heterocyclesp. 125
Reduction of Sulfur Compoundsp. 125
N-O Reductionsp. 125
C-C Multiple Bond Reductionsp. 126
C=C Reductionsp. 126
C[identical with]C Reductionsp. 129
Hetero Bond Reductionsp. 130
C-O to C-Hp. 130
C-Hal to C-Hp. 131
C-S to C-Hp. 131
Reductive Cleavagesp. 132
Oxiranesp. 132
N-O Cleavagesp. 132
Other Reductive Cleavagesp. 133
Reduction of Azidesp. 133
Other Reductionsp. 134
Synthesis of Heterocycles
Oxiranes, Aziridines, and Thiiranesp. 135
Oxetanes, Azetidines, and Thietanesp. 139
Lactamsp. 139
Lactonesp. 145
Furans and Thiophenesp. 150
Pyrroles, Indoles, etcp. 158
Pyridines, Quinolines, etcp. 166
Pyrans, Pyrones, and Sulfur Analoguesp. 174
Other Heterocycles with One Heteroatomp. 180
Heterocycles with a Bridgehead Heteroatomp. 182
Heterocycles with Two or More Heteroatomsp. 184
Heterocycles with 2 N'sp. 184
5-Memberedp. 184
6-Memberedp. 188
7-Memberedp. 191
Heterocycles with 2 O's or 2 S'sp. 192
Heterocycles with 1 N and 1 Op. 194
Heterocycles with 1 N and 1 Sp. 200
Heterocycles with 1 O and 1 Sp. 202
Heterocycles with 3 or more N'sp. 203
Heterocycles with 2 N's and 1 Op. 205
Heterocycles with 2 N's and 1 Sp. 206
Other Heterocyclesp. 206
Reviewsp. 208
Protecting Groups
Aldehyde and Ketone Protecting Groupsp. 215
Amino Acid Protecting Groupsp. 218
Amine Protecting Groupsp. 219
Carboxyl Protecting Groupsp. 221
Hydroxyl Protecting Groupsp. 222
Other Protecting Groupsp. 226
Useful Synthetic Preparations
Functional Group Preparationsp. 227
Acetals and Ketalsp. 227
Acids and Anhydridesp. 229
Alcohols and Related Species (see also: II.B.1, III.A., V.E., VI.A.9)p. 230
Aldehydes and Ketones (see also: I.A.1., I.G.2., II.A.1)p. 232
Amides and Related Speciesp. 234
Aminesp. 238
Amino Acid Derivativesp. 242
Azidesp. 246
Carbohydratesp. 247
Esters (see also: I.G.2., IV.D., V.D., VI.A.3)p. 248
Ethersp. 252
Halides (see also: II.B.2.)p. 253
Nitriles and Iminesp. 256
Other N-Containing Functional Groupsp. 258
Additions to Alkenes and Alkynesp. 260
Boron Compoundsp. 262
Nucleosides, Nucleotides, etcp. 263
Phosphorus, Selenium and Tellurium Compoundsp. 265
Silicon Compoundsp. 267
Sulfur Compoundsp. 268
Tin Compoundsp. 272
Reviews
Techniquesp. 274
Asymmetric Synthesis and Molecular Recognitionp. 276
Reactionsp. 281
Reactive Intermediatesp. 286
Organometallics and Metalloidsp. 288
Halogen Compounds and Halogenation (see also: VI.A.11.)p. 293
Natural Productsp. 294
Others (see also: IV.M, VIII.A.5, VIII.C.6, VIII.F.7)p. 301
Selected Topical Areas
Fullerene Chemistryp. 305
Diels-Alder Type Cycloadditionsp. 305
Other Cycloadditionsp. 305
Photochemical Reactionsp. 306
Other Fullerene Chemistryp. 306
Taxol and Related Taxane Chemistryp. 310
Dendrimers, Calixarenes and Other Unnatural Productsp. 312
Dendrimersp. 312
Dendrimer Synthesisp. 312
Dendrimer Catalystsp. 316
Hetero-Containing & Miscellaneous Dendrimersp. 316
Calixeranesp. 317
Calixarene Receptorsp. 317
Synthesis of Calixiranep. 319
Synthesis on Calixiranesp. 321
Calixirane Isolation, Conformation, etcp. 323
Rotaxanesp. 323
Supramoleculesp. 324
Cyclophanesp. 327
Otherp. 329
Reviewsp. 330
Total Syntheses of Selected Natural Products (see also: VIII.B and VIII.C)p. 332
Reactions in Polar Mediap. 347
Reactions in Aqueous Mediap. 347
Reactions in Ionic Mediap. 350
Combinatorial Chemistryp. 355
Supports, Linkers and Protecting Groupsp. 355
Supported Reagents, Catalysts, Ligands and Scavengersp. 357
Solid-Phase Heterocyclic Synthesisp. 359
Solid-Supported Organic Reaction Processesp. 363
Targeted Library Synthesisp. 367
Novel Techniques in Combinatorial Chemistryp. 371
Reviewsp. 372
Author Indexp. 375
Table of Contents provided by Ingram. All Rights Reserved.

ISBN: 9780120408337
ISBN-10: 0120408333
Series: Annual Reports in Organic Synthesis
Audience: General
Format: Paperback
Language: English
Number Of Pages: 432
Published: 1st November 2003
Publisher: ACADEMIC PR INC
Country of Publication: US
Dimensions (cm): 22.91 x 15.19  x 2.26
Weight (kg): 0.58
Edition Type: Revised