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Smith M.B., March J. — March's Advanced Organic Chemistry: Reactions, Mechanisms, and Structure
Smith M.B., March J. — March's Advanced Organic Chemistry: Reactions, Mechanisms, and Structure



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Название: March's Advanced Organic Chemistry: Reactions, Mechanisms, and Structure

Авторы: Smith M.B., March J.

Аннотация:

"March has been uncompromising in his search for clarity and utility in presentations of a wide variety of essential organic chemistry. It remains an accessible and useful tool for both specialists and nonspecialists in the field. It does an excellent job both as a text for first-year graduate students and a handy reference for others."-Journal of Chemical Education "The ratio of information to price makes this book a wonderful bargain."-American Scientist
New to this Fifth Edition:
* Michael Smith from the University of Connecticut joins as coauthor for the Fifth Edition
* Contains 20,000 valuable, selected references to the primary literature-5,000 new to this edition
* 40 entirely new sections covering the most important developments in organic chemistry since the previous edition
* Updated illustrations of molecular structures


Язык: en

Рубрика: Химия/

Статус предметного указателя: Готов указатель с номерами страниц

ed2k: ed2k stats

Издание: 5-th edition

Год издания: 2001

Количество страниц: 2083

Добавлена в каталог: 21.02.2007

Операции: Положить на полку | Скопировать ссылку для форума | Скопировать ID
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Предметный указатель
Aldehydes oxidation of, mechanism      917
Aldehydes oxidation with permanganate      918
Aldehydes oxidation, reagents for      917
Aldehydes oxidative cleavage      1521
Aldehydes photochemical cleavage      318
Aldehydes reaction with $LiAlH_4$      533
Aldehydes reaction with $Me_3Al$ or $Me_2TiCl_2$      1210
Aldehydes reaction with $Me_3SiCN$      1240
Aldehydes reaction with $PCl_5$      1195
Aldehydes reaction with $TiCl_3/Zn-Cu$      1561
Aldehydes reaction with $\alpha$-methoxyvinyllithium      1227
Aldehydes reaction with active methylene compounds      1225—1228
Aldehydes reaction with acyl halides      1182
Aldehydes reaction with alcohols      1180 1182
Aldehydes reaction with aldehydes      1218—1223
Aldehydes reaction with alkenes      1038 1249—1250
Aldehydes reaction with allylsilanes      1211
Aldehydes reaction with amides      1187
Aldehydes reaction with amines      552 1185—1189
Aldehydes reaction with ammonia      925 1186 1188
Aldehydes reaction with anhydrides      1229 1245
Aldehydes reaction with base and then imines      1222
Aldehydes reaction with bisulfites      1185
Aldehydes reaction with boron carbanions      785
Aldehydes reaction with bromine      914 1196
Aldehydes reaction with bromoesters and Zn      1212
Aldehydes reaction with carboxylic acids, and isonitriles      1251
Aldehydes reaction with chlorine      914
Aldehydes reaction with chloro esters      1230
Aldehydes reaction with conjugated compounds      1212
Aldehydes reaction with cyanide and conjugated compounds      1033
Aldehydes reaction with diazo esters      785
Aldehydes reaction with diazoalkanes      1248
Aldehydes reaction with diazomethane      1248
Aldehydes reaction with dichromate      918
Aldehydes reaction with diethyl diazoacetate      785
Aldehydes reaction with diethylzinc      1211
Aldehydes reaction with dithiols      556
Aldehydes reaction with esters      1223
Aldehydes reaction with formaldehyde      1230
Aldehydes reaction with Girard’s reagents T and P      1193
Aldehydes reaction with Grignard reagents      1205—1209
Aldehydes reaction with halogens      775
Aldehydes reaction with HCN      1239
Aldehydes reaction with hydrazines      1192—1193
Aldehydes reaction with hydrazones      1193
Aldehydes reaction with hydrogen sulfide      1184
Aldehydes reaction with hydroxylamine      1194
Aldehydes reaction with hydroxylamme and formic acid      1195
Aldehydes reaction with KCN      1243
Aldehydes reaction with ketene acetals      1249
Aldehydes reaction with ketenes      1249
Aldehydes reaction with ketones      1218—1223
Aldehydes reaction with Lawesson’s reagent      1184
Aldehydes reaction with Mannich bases      1189
Aldehydes reaction with NBS      914
Aldehydes reaction with organocerium reagents      1205
Aldehydes reaction with organocuprates      1205
Aldehydes reaction with organolithium reagents      1205—1209
Aldehydes reaction with organometallics      1209—1211
Aldehydes reaction with oxidizing agents      917
Aldehydes reaction with Petasis reagent      1238
Aldehydes reaction with phenylhydrazine      1453
Aldehydes reaction with phosphorus ylids      1231—1237
Aldehydes reaction with semicarbazide      1193
Aldehydes reaction with silane carbanions      1228
Aldehydes reaction with silanes      1239
Aldehydes reaction with silyl enol ethers      552
Aldehydes reaction with silyl ketene acetals      1223
Aldehydes reaction with sodium $azide/MnO_2$      516
Aldehydes reaction with sulfur ylids      1247
Aldehydes reaction with Tebbe’s reagent      1238
Aldehydes reaction with thiols      1181 1185
Aldehydes reaction with triphenyl phosphite      1196
Aldehydes reaction with water      1175
Aldehydes reduction of      1197—1203
Aldehydes reduction with boranes      1200
Aldehydes reduction with hydrazine-KOH      1547
Aldehydes reduction with hydrides      1197—1198
Aldehydes reduction with metals in water      1200
Aldehydes reduction with silanes and base      1200
Aldehydes reduction with sodium in ethanol      1199
Aldehydes reduction with Zn-Hg/HCl      1547
Aldehydes reduction, chemoselective      1198
Aldehydes reductive amination      1188
Aldehydes reductive coupling      1559—1561
Aldehydes reductive dimerization      1182
Aldehydes reductive removal of O      1547
Aldehydes trimerization of      1245
Aldehydes, aromatic and the Duff reaction      717
Aldehydes, aromatic and the Tishchenko reaction      1565
Aldehydes, aromatic by bromination of methyl aryls      1534
Aldehydes, aromatic by the Etard reaction      1534
Aldehydes, aromatic by the Gatterman reaction      715
Aldehydes, aromatic by the Gatterman — Koch reaction      715
Aldehydes, aromatic by the Reimer — Tiemann reaction      716
Aldehydes, aromatic by the Vilsmeier reaction      715
Aldehydes, aromatic decarbonylation      732
Aldehydes, aromatic from aromatic compounds      715
Aldehydes, aromatic from methyl aryls      1533
Aldehydes, aromatic oxidation of      1528
Aldehydes, aromatic reaction with $Al(OEt)_3$      1565
Aldehydes, aromatic reaction with sulfuric acid      732
Aldehydes, chiral, in the aldol reaction      1222
Aldehydes, conjugated and Michael reactions      1022—1024
Aldehydes, conjugated and the Grignard reaction      1205
Aldehydes, conjugated by [2,3] sigmatropic rearrangement      1454
Aldehydes, conjugated reaction with borane      1031
Aldehydes, conjugated reaction with organocuprates      1027
Aldehydes, rearrangement of      1401
Aldimines      see “Imines”
Aldol condensation      236 552 1218—1223
Aldol reaction      236 552 1218—1223
Aldol reaction crossed      1221
Aldol reaction crossed, and the TollenV reaction      1231
Aldol reaction homoaldol      1227
Aldol reaction intramolecular      1222
Aldol reaction intramolecular, and the Robinson annulation      1222
Aldol reaction Mukaiyama      1223
Aldol reaction retro      808
Aldols      150 1220
Aldrich Library of Spectra      1619
Algorithm, for solvent dielectric effects      450
Alkaloids, Cinchona, and dihydroxylation of alkenes      1050
Alkanes      also see “Hydrocarbons”
Alkanes addition to alkenes      1017
Alkanes by Clemmensen reduction      1648
Alkanes by the Barton — McCombie reaction      1647
Alkanes by the Haller — Bauer reaction      1648
Alkanes by the Kolbe reaction      1648
Alkanes by the Wurtz reaction      1647
Alkanes by Wolff — Kishner reduction      1648
Alkanes catalytic exchange with deuterium      1005
Alkanes conformations      168
Alkanes cyclic, aromatization      1510
Alkanes from addition of alkanes to alkenes      1648
Alkanes from addition of organometallics to alkenes      1648
Alkanes from addition of organometallics to alkynes      1648
Alkanes from addition to alkenes      1648
Alkanes from alkyl halides with organocuprates      1647
Alkanes from alkyl halides with organometallics      1647
Alkanes from alkylation of alkanes      1648
Alkanes from carboxylic acids with trimethylaluminum      1648
Alkanes from cleavage of alkanes      1648
Alkanes from cleavage of ketones with amide ion      1648
Alkanes from cleavage of nonenolizable ketones      1648
Alkanes from cleavage of tertiary alkoxides      1648
Alkanes from coupling of alcohols      1647
Alkanes from coupling of alkanes      1648
Alkanes from coupling of alkyl halides      1647
Alkanes from coupling of boranes      1648
Alkanes from coupling of Grignard reagents      1648
Alkanes from coupling of organometallic compounds      1648
Alkanes from decarbonylation of acyl halides      1648
Alkanes from decarbonylation of aldehydes      1648
Alkanes from decarboxylation of carboxylic acids      1648
Alkanes from decarboxylative dimerization      1648
Alkanes from decyanation of nitrites      1648
Alkanes from deoxygenation of aryl ethers      1648
Alkanes from desulfurization of sulfur compounds      1648
Alkanes from dimerization of alkenes      1648
Alkanes from extrusion of $CO_2$ from diacyl peroxides      1648
Alkanes from Grignard reagents and ethers      1647
Alkanes from hydrogenation of alkenes      1648
Alkanes from hydrogenation of alkynes      1648
Alkanes from hydrogenolysis of alcohols      1647
Alkanes from hydrogenolysis of esters      1647
Alkanes from hydrogenolysis of nitriles      1647
Alkanes from insertion of carbenes      1648
Alkanes from ketones with trimethylaluminum      1648
Alkanes from organometallic compounds and acids      1648
Alkanes from organometallic reagents and alkyl sulfates      1647
Alkanes from organometallic reagents and alkyl sulfonates      1647
Alkanes from oxidation of hydrazines      1648
Alkanes from oxidative decarboxylation of carboxylic acids      1648
Alkanes from reduction of aldehydes or ketones      1648
Alkanes from reduction of alkenes      1648
Alkanes from reduction of alkyl halides      1647
Alkanes from reduction of alkynes      1648
Alkanes from reduction of aromatic rings      1648
Alkanes from reduction of carboxylic acids      1648
Alkanes from reduction of cyano to methyl groups      1648
Alkanes from reduction of dithianes      1647
Alkanes from reduction of epoxides      1648
Alkanes from reduction of esters      1648
Alkanes from reduction of the С — N bond      1647
Alkanes from reduction of tosylates      1647
Alkanes from reductive cleavage of carboxylic esters      1647
Alkanes from reductive cleavage of cyclopropanes      1648
Alkanes from reductive cleavage of sulfides      1647
Alkanes from reductive cleavage of sulfoxides      1647
Alkanes from reductive cleavage of thiols      1647
Alkanes radical halogenation, mechanism of      909
Alkanes rate of radical abstraction      901
Alkanes reaction with halogens      907—911
Alkene acids, cyclization of      1043
Alkene alcohols by the Prins reaction      1241
Alkene alcohols conversion to halo ethers      1056
Alkene alcohols fragmentation      1351
Alkene alcohols from aldehydes and silanes      1239
Alkene alcohols from alkenes and formaldehyde      1241
Alkene aldehydes by oxy-Cope rearrangement      1445
Alkene aldehydes from diene alcohols      1445
Alkene amides, cyclization of      1043
Alkene amines, from alkenes      782
Alkene ketones by Claisen rearrangement      1452
Alkene ketones from allyl vinyl ethers      1452
Alkene metathesis      1457—1459; see “Metathesis alkene”
Alkenes acylation and Markovnikov’s rule      784
Alkenes acylation of      784
Alkenes acyloxylation      1033
Alkenes addition and exo/endo diastereoselectivity      987
Alkenes addition and reactivity      981
Alkenes addition of aldehydes      1033
Alkenes addition of alkanes      1017
Alkenes addition of aniline      1001
Alkenes addition of carbanions      1018
Alkenes addition of formamides      1034
Alkenes addition of formates      1034
Alkenes addition of nucleophilic radicals      983
Alkenes addition of organometallics      1024—1026
Alkenes addition of silanes      1018 1039
Alkenes addition of water      974
Alkenes addition to alkenes      1019
Alkenes addition to and antiaromaticity      983
Alkenes addition to and hyperconjugation      987
Alkenes addition to and the Cieplak effect      988
Alkenes addition to, electronic effects      987
Alkenes addition to, field effects      987
Alkenes addition, cyclic mechanisms      979
Alkenes addition, regioselectivity      984
Alkenes alkylation by the Prins reaction      1047
Alkenes alkylation of      1047
Alkenes ally lie oxidation, reagents for      915
Alkenes allylic rearrangement      771
Alkenes aminosulfenylation      1058
Alkenes and alkene formation from boranes      1338
Alkenes and allylic radicals      902
Alkenes and Birch reduction      1008
Alkenes and Bredt's rule      188
Alkenes and cis/trans isomers      157—160
Alkenes and diastereomers      157—160
Alkenes and Friedel — Crafts acylation      784
Alkenes and Friedel — Crafts alkylation      710
Alkenes and LIDAKOR      1329
Alkenes and Markovnikov’s rule      984
Alkenes and organolithium reagents      1649
Alkenes and PES      12
Alkenes and phase transfer conditions      1085
Alkenes and radical bromination      911
Alkenes and Tebbe’s reagent      1649
Alkenes and termolecular addition      972
Alkenes and the Barbier — Wieland procedure      1526
Alkenes and the Bayer test      1049
Alkenes and the CIP method      157
Alkenes and the Heck reaction      930
Alkenes and the Michael reaction      1022—1024
Alkenes and the Paterno — Buechi reaction      1249
Alkenes and the Petasis reagent      1649
Alkenes and thermolysis of aziridines      1061
Alkenes and Wohl — Ziegler bromination      911
Alkenes anti-Bredt and the Wittig reaction      1233
Alkenes anti-Bredt anti-Markovnikov addition      991 994
Alkenes Bakers yeast reduction      1004
Alkenes by Chugaev elimination      1649
Alkenes by Cope elimination      1333 1649
Alkenes by Cope rearrangement      1650
Alkenes by diazonium ions      1335
Alkenes by E2 elimination      1304
Alkenes by extrusion reactions      1650
Alkenes by Hofmann elimination      1331 1649
Alkenes by McMurry reaction      1561
Alkenes by Meerwein arylation      1649
Alkenes by Peterson olefination      1649
Alkenes by protonation of vinylboranes      1425
Alkenes by remote dehydrogenation      1650
Alkenes by the Bamford — Stevens reaction      1335
Alkenes by the Boord reaction      1344 1650
Alkenes by the Chugaev reaction      1330
Alkenes by the Corey — Winter reaction      1340
Alkenes by the Demyanov rearrangement      1650
Alkenes by the di-$\pi$-methane rearrangement      1650
Alkenes by the Diels — Alder reaction      1649
Alkenes by the ene reaction      1021 1649
Alkenes by the Horner — Emmons reaction      1233
Alkenes by the Peterson alkenylation reaction      1228
Alkenes by the Ramberg — Backlund reaction      1341 1650
Alkenes by the Reformatsky reaction      1649
Alkenes by the Shapiro reaction      1334
Alkenes by the Vilsmeier reaction      785
Alkenes by the Wadsworth — Emmons reaction      1233
Alkenes by the Wittig reaction      1231—1237
Alkenes by the Wittig — Horner reaction      1233
Alkenes by the Wurtz reaction      535
Alkenes by twofold extrusion      1355
Alkenes by Wagner — Meerwein rearrangement      1650
Alkenes by Wittig olefination      1231—1237 1649
Alkenes carbocation intermediates      974
Alkenes carbocations and Friedel — Crafts alkylation      710
Alkenes carbonylation of, with alkenes      1035
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