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Carey F.A., Sundberg R.J. — Advanced organic chemistry (Part B)
Carey F.A., Sundberg R.J. — Advanced organic chemistry (Part B)



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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: en

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
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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, $\alpha$-halo, Ramberg — Backlund rearrangement of      604—607
Sulfones, $\beta$-hydroxy, reductive elimination      314
Sulfones, reductive elimination of      343
Sulfones, vinyl, as dienophiles      342—343
Sulfonium ylides, [2,3-]sigmatropic rearrangement of      395
Sulfoxides, $\alpha$-alkylthio, as acyl anion equivalent      841
Sulfoxides, $\beta$-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-$TiCL_4$ 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, $\beta$-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
1 2 3 4 5 6
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