Авторизация
Поиск по указателям
Carey F.A., Sundberg R.J. — Advanced organic chemistry (Part B)
Обсудите книгу на научном форуме
Нашли опечатку? Выделите ее мышкой и нажмите Ctrl+Enter
Название: Advanced organic chemistry (Part B)
Авторы: Carey F.A., Sundberg R.J.
Аннотация: Since its original appearance in 1977, Advanced Organic Chemistry has found wide use as a text providing broad coverage of the structure, reactivity and synthesis of organic compounds. The Fourth Edition provides updated material but continues the essential elements of the previous edition. The material in Part A is organized on the basis of fundamental structural topics such as structure, stereochemistry, conformation and aromaticity and basic mechanistic types, including nucleophilic substitution, addition reactions, carbonyl chemistry, aromatic substitution and free radical reactions. The material in Part B is organized on the basis of reaction type with emphasis on reactions of importance in laboratory synthesis. As in the earlier editions, the text contains extensive references to both the primary and review literature and provides examples of data and reactions that illustrate and document the generalizations. While the text assumes completion of an introductory course in organic chemistry, it reviews the fundamental concepts for each topic that is discussed. The Fourth Edition updates certain topics that have advanced rapidly in the decade since the Third Edition was published, including computational chemistry, structural manifestations of aromaticity, enantioselective reactions and lanthanide catalysis. The two parts stand alone, although there is considerable cross-referencing. Part A emphasizes quantitative and qualitative description of structural effects on reactivity and mechanism. Part B emphasizes the most general and useful synthetic reactions. The focus is on the core of organic chemistry, but the information provided forms the foundation for future study and research in medicinal and pharmaceutical chemistry, biological chemistry and physical properties of organic compounds.
Язык:
Рубрика: Химия /
Статус предметного указателя: Готов указатель с номерами страниц
ed2k: ed2k stats
Издание: 4th edition
Год издания: 1938
Количество страниц: 965
Добавлена в каталог: 16.04.2006
Операции: Положить на полку |
Скопировать ссылку для форума | Скопировать ID
Предметный указатель
Stannaries, allylic, reactions with carbocations 596
Stannaries, allylic, reactions with ketones 580
Stannaries, allylic, reactions with thioacetals 583
Stannaries, aryl, palladium-catalyzed coupling 511—514
Stannaries, as hydrogen atom donors 288—290
Stannaries, halo, reactions with carbonyl compounds 580—581
Stannaries, halo, reactions with organometallic compounds 579
Stannaries, metal-metal exchange reactions of 444
Stannaries, palladium-catalyzed reactions with acid chlorides 525
Stannaries, synthesis of 576—579
Stannaries, trialkyl, as hydrogen atom donors 288—290 657—658
stereochemistry, control of in synthesis 846—848
Stereoselectivity of, addition of hydrogen halides to alkenes 193—194
Stereoselectivity of, aldol addition 64—71
Stereoselectivity of, amine oxide pyrolysis 409
Stereoselectivity of, Claisen rearrangement 388—392
Stereoselectivity of, Cope rearrangement 376—380
Stereoselectivity of, Diels — Alder reaction 334 349—353 355—357
Stereoselectivity of, dihydroxylation of alkenes 758—760
Stereoselectivity of, epoxidation of alkenes 764—766
Stereoselectivity of, epoxidation of allylic alcohols 760—764
Stereoselectivity of, hydroboration of alkenes 230 236—238
Stereoselectivity of, hydrogenation of alkenes 250—259
Stereoselectivity of, iodolactonization 206—207
Stereoselectivity of, oxymercuration 199—200
Stereoselectivity of, Wittig reaction 112—113
Stille reaction 511—515
Sulfenyl halides, addition reactions of 209—213
Sulfides, conversion to organolithium compounds 437
Sulfonamides, as amine protecting groups 834
Sulfonamides, N-alkylation of 156
Sulfonamides, radical reactions of 656
Sulfonates, mono-, of diols, rearrangement of 604—607
Sulfonates, preparation from alcohols 141—142 154
Sulfonates, reaction with Grignard reagents 446
Sulfonates, reduction of 313 315
Sulfones, -halo, Ramberg — Backlund rearrangement of 604—607
Sulfones, -hydroxy, reductive elimination 314
Sulfones, reductive elimination of 343
Sulfones, vinyl, as dienophiles 342—343
Sulfonium ylides, [2,3-]sigmatropic rearrangement of 395
Sulfoxides, -alkylthio, as acyl anion equivalent 841
Sulfoxides, -keto 109—110
Sulfoxides, alkylation of 158
Sulfoxides, allylic, [2,3]-sigmatropic rearrangement of 395
Sulfoxides, vinyl, as dienophiles 342—343
Sulfoximines, reactions of 126
Sulfur ylides 122—126
Swern oxidation 753
Synthetic analysis 845—846
Synthetic equivalent groups 13 839—845
Synthetic equivalent groups, in Diels — Alder reactions 340—342
t-butoxycarbonyl, as protecting group 831 897—898
Taxol, synthesis of 881—890
Tetrabromocyclohexadienone, as brominating reagent 145 209 218
Tetramethylethylenediamine, solvation by 23 438—439
Thallium, organo- compounds, preparation by electrophilic thallation 713—714
Thermodynamic control, of enolate formation 5-8
Thioamides, alkylation of 158
Thiocarbonates, reductive elimination of 290 887
Thiocyanogen, as reagent 217
Thioesters, reductive deoxygenation 290
Thioketals, desulfurization of 309
Thiols, alkylation of 158
Tiffeneau — Demjanov rearrangement 608
Tin, organo- compounds see “Stannanes”
Titanium tetraisopropoxide, as catalyst for epoxidation of allylic alcohols 762—764
TMEDA see “Tetramethylethylenediamine”
Tri-n-butyltin hydride, in radical generating reactions 652 660—664 665—667 674 677—678
Tri-n-butyltin hydride, reductive dehalogenation by 288—289
Trialkylborohydrides, as reducing agents 267 276 278 280 284
Triazenes, from aromatic diazonium ions 715
Triazenes, in conversion of carboxylic acids to esters 153
Triethyl orthoformate, reaction with Grignard reagents 451
Trifluoromethanesulfonates, alkenyl, palladium-catalyzed carbonylation 522
Trifluoromethanesulfonates, alkenyl, palladium-catalyzed reaction with alkenyl stannanes 525
Trifluoromethanesulfonates, alkenyl, preparation from ketones 515
Trifluoromethanesulfonates, alkyl, preparation from alcohols 142
Trimethyloxonium tetrafluoroborate, alkylation of amides by 156
Trimethylsilyl iodide, cleavage of esters by 163
Trimethylsilyl iodide, cleavage of ethers by 163
Trimethylsilyl iodide, generation in situ 163
Triphenylphosphine, in preparation of alkyl halides 146
Triphenylphosphine, in Wittig reaction 111
Tris(trimethylsilyl)silane, as hydrogen atom donor 658 664
Ugi reaction 906
Ullman coupling reaction 495—498
Umpolung 839
Vanadyl acetylacetonate, as catalyst for epoxidation of allylic alcohols 760—762
Vilsmeier — Haack reaction 711
Wacker reaction 501
Wadsworth — Emmons reaction 116—117
Wang linker, in oligonucleotide synthesis 899
Wilkinson's catalyst, hydrogenation with 253
Wilkinson's catalyst, in hydroboration 229
Wilkinson's catalyst, reduction of enones using triethylsilane 273
Wittig reaction 57 111—119
Wittig reaction, in synthesis of epothilone A 893
Wittig reaction, intramolecular 117
Wittig reaction, stereoselectivity of 112—113
Wittig rearrangement 397—399
Wolff rearrangement 641—642
Wolff — Kishner reduction 307
X-ray structure of, 2-methylpropenal-BF3 complex 337
X-ray structure of, ethylmagnesium bromide 434
X-ray structure of, lithium anion of N-phenylimine of methyl t-butyl ketone 35
X-ray structure of, lithium enolate of methyl t-butyl ketone 24
X-ray structure of, O-acryloyl lactate- complex 337
X-ray structure of, phenyllithium 439
X-ray structure of, potassium enolate of methyl t-butyl ketone 24
Xanthate, ester pyrolysis 413
Xanthate, in preparation of alkyl chlorides 143
Xanthate, radicals from 658
Ylide, carbonyl from carbenes 637—638
Ylide, oxonium from carbenes 639
Ylide, phosphorus 111—116
Ylide, phosphorus, -oxido 116
Ylide, phosphorus, functionalized 116
Ylide, sulfur 122—126
Zinc borohydride 266 270
Zinc, organo- compounds 459—463
Zinc, organo- compounds, enantioselective addition to aldehydes 461—462
Zinc, organo- compounds, in cyclopropanation by methylene iodide 626
Zinc, organo- compounds, in palladium-catalyzed coupling reactions 508
Zinc, organo- compounds, mixed copper-zinc compounds 489—491 495
Zinc, organo- compounds, nickel-catalyzed coupling 529
Zinc, organo- compounds, preparation of 459-461
Zinc, organo- compounds, Reformatsky reaction of 462
[2,3]-sigmatropic rearrangements 394—399
[2,3]-sigmatropic rearrangements, of allylic amine oxides 397
[2,3]-sigmatropic rearrangements, of allylic ethers 397—399
[2,3]-sigmatropic rearrangements, of allylic selenoxides 395 806
[2,3]-sigmatropic rearrangements, of allylic sulfonium ylides 395
[2,3]-sigmatropic rearrangements, of allylic sulfoxides 395
[2,3]-sigmatropic rearrangements, of ammonium ylides 395—396
[2,3]-sigmatropic rearrangements, of S-anilinosulfonium ylides 397
[3,3]-sigmatropic rearrangements 376—394
[3,3]-sigmatropic rearrangements, anionic oxy-Cope 382
[3,3]-sigmatropic rearrangements, Claisen 383—394
[3,3]-sigmatropic rearrangements, Cope 376—383
[3,3]-sigmatropic rearrangements, of ester silyl enol ethers 389—391
[3,3]-sigmatropic rearrangements, of unsaturated iminium ions 574
[3,3]-sigmatropic rearrangements, oxy-Cope 382—383
Реклама