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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
Alcohols by reduction aldehydes or ketones      1197—1203
Alcohols by the Baeyer-Villiger reaction      1644
Alcohols by the Barbier reaction      1205
Alcohols by the Bouveault-Blanc procedure      1551
Alcohols by the Cannizzaro reaction      1200 1564 1644
Alcohols by the Demyanov rearrangement      1644
Alcohols by the Tamao-Fleming oxidation      482
Alcohols by the Wittig rearrangement      1421 1644
Alcohols by Wagner-Meerwein rearrangement      1644
Alcohols conversion to ethers      479
Alcohols coupling by $ML_i-TiCl_3$      544
Alcohols cyclic, oxidative cleavage      1521
Alcohols cyclic, transannular etherincation      920
Alcohols dehydration of      479 1326
Alcohols dehydration, and Zaitsev’s rule      1327
Alcohols dehydrogenation      1515
Alcohols enzymatic oxidation      1517
Alcohols epoxy, ring opening      462
Alcohols from acetals      1643
Alcohols from acid derivatives      567 1214 1551 1644
Alcohols from alcohols      1393 1643
Alcohols from aldehydes      719 1564 1643—1644
Alcohols from aldehydes and organometallics      1209—1211
Alcohols from alkaline cleavage of ethers      1644
Alcohols from alkanes      1533
Alcohols from alkenes      914 974 993 1643 1643 1644
Alcohols from alkenes, reagents for      914
Alcohols from allylic alcohols      1643
Alcohols from allylic silanes      1643
Alcohols from allylic silanes to aldehydes      1644
Alcohols from amides      1644
Alcohols from amines      494 1398 1643
Alcohols from anhydrides      1644
Alcohols from aromatic compounds      719 1643
Alcohols from boradioxolanes      1422
Alcohols from boranes      796 1422 1423 1644
Alcohols from carboxylic acids      1549 1644
Alcohols from contraction of rings      1644
Alcohols from cyclopropanes      1643
Alcohols from epoxides      529 546 1643
Alcohols from esters      1214 1551 1643 1644
Alcohols from ethers      1421 1643
Alcohols from expansion of rings      1644
Alcohols from Grignard reagents and aldehydes or ketones      795 1205—1209 1644
Alcohols from hydrolysis of alkyl halides      1643
Alcohols from hydrolysis of carboxylic esters      1643
Alcohols from hydrolysis of enol acetals      1643
Alcohols from hydrolysis of enol ethers      1643
Alcohols from hydrolysis of inorganic esters      1643
Alcohols from hydrolysis of ortho esters      1643
Alcohols from hydrolysis of sulfonic esters      1643
Alcohols from hydroperoxides      1558 1644
Alcohols from hydroxyalkylation of aromatic rings      1643
Alcohols from hydroxylation at an aliphatic carbon      1643
Alcohols from hydroxylation of silanes      482
Alcohols from hydroxymethylation of aromatic rings      1643
Alcohols from ketones      719 1209—1211 1643—1644
Alcohols from nitrites      1644
Alcohols from organolithium reagents and aldehydes or ketones      1205—1209 1644
Alcohols from organometallic compounds and alcohols      1643
Alcohols from organometallic compounds and aldehydes      1644
Alcohols from organometallic compounds and epoxides      1643
Alcohols from organometallic compounds and ketones      1644
Alcohols from organometallic reagents and oxygen      1643
Alcohols from ortho esters      1643
Alcohols from ozonides      1644
Alcohols from peroxides      1558
Alcohols from radicals and aldehydes or ketones      1644
Alcohols from rearrangement of alcohols      1644
Alcohols from rearrangement of alkenes      1644
Alcohols from rearrangement of ethers      1644
Alcohols from rearrangements of allylic ethers      1644
Alcohols from rearrangements of allylic sulfoxides      1644
Alcohols from reduction of esters      1644
Alcohols from transesterification      1643
Alcohols hydrogenation of      527
Alcohols hydrogenolysis of      527
Alcohols methyl and the haloform reaction      813
Alcohols methyl optically active, by hydroboration      1014
Alcohols methyl order of acid strength      350
Alcohols methyl oxidation to aldehydes or ketones      1514—1517
Alcohols methyl oxidation to cyclic ethers      919
Alcohols methyl oxidation with Bacillus steamthermophilus      1517
Alcohols methyl oxidation with chromate, mechanism      1517
Alcohols methyl oxidation with chromic acid      1515
Alcohols methyl oxidation with chromium derivatives      1537
Alcohols methyl oxidation with Collins’ reagent      1514
Alcohols methyl oxidation with Corey’s reagent      1515
Alcohols methyl oxidation with DMSO-based reagents      1515—1516
Alcohols methyl oxidation with Fremy's salt      1515
Alcohols methyl oxidation with hypervalent iodine reagents      1516
Alcohols methyl oxidation with Jones reagent      1514
Alcohols methyl oxidation with nitroxyl radical      1515
Alcohols methyl oxidation with oxoammonium salts      1515
Alcohols methyl oxidation with permanganate, and ultrasound      1515
Alcohols methyl oxidation with pyridinium chlorochromate      1514
Alcohols methyl oxidation with pyridinium dichromate      1514
Alcohols methyl oxidation with ruthenium tetroxide      1515
Alcohols methyl oxidation with TEMPO-NCS      1515
Alcohols methyl oxidation with zirconocene complexes      1515
Alcohols methyl oxidation withTPAP      1515
Alcohols methyl oxidation, and microwaves      1515
Alcohols methyl photochemical addition to alkenes      997
Alcohols oxidation of silanes      1643
Alcohols oxidative dehydrogenation with copper chromite      1515
Alcohols reaction with $POCl_3$      493
Alcohols reaction with $PPh_3$ and $Cbr_4$      519
Alcohols reaction with acyl halides      482
Alcohols reaction with aldehydes or ketones      1180
Alcohols reaction with alkenes      996
Alcohols reaction with alkyl halides      564
Alcohols reaction with amides      488
Alcohols reaction with anhydrides      483
Alcohols reaction with aryl halides      870
Alcohols reaction with carbon disulfide      1184
Alcohols reaction with carboxylic acids      484—486
Alcohols reaction with chlorotrimethylsilane      527
Alcohols reaction with cyanogen chloride      1183
Alcohols reaction with DAST      519
Alcohols reaction with diazo compounds      479
Alcohols reaction with diazomethane      479
Alcohols reaction with dihydropyran      996
Alcohols reaction with diisopropyl azodicarboxylate      502
Alcohols reaction with enol esters      487
Alcohols reaction with enol ethers      487
Alcohols reaction with esters      486
Alcohols reaction with ethers      480
Alcohols reaction with Grignard reagents      526
Alcohols reaction with HI      518
Alcohols reaction with hydrazoic acid      502
Alcohols reaction with isocyanates      1182—1183
Alcohols reaction with isothiocyanates      1183
Alcohols reaction with lactones      487
Alcohols reaction with Lawesson’s reagent      496
Alcohols reaction with lead tetraacetate      919
Alcohols reaction with nitrites      1183 1244
Alcohols reaction with nitrous acid      493
Alcohols reaction with onium salts      482
Alcohols reaction with phosgene      483
Alcohols reaction with phosphorus halides      518
Alcohols reaction with sulfonamides      576
Alcohols reaction with sulfonyl chlorides      576
Alcohols reaction with sulfur trioxide      493
Alcohols reaction with thionyl chloride      493 518
Alcohols reaction with triflic anhydride      493
Alcohols reaction with trimethylaluminum      544
Alcohols reactivity with alkenes      996
Alcohols reagents for hydrogenolysis      527
Alcohols vinyl cyclic, and sigmatropic rearrangements      1440
Alcohols, alkenyl, fragmentation      1351
Alcohols, alkynyl, dehydration of      1327
Alcohols, allylic by Mislow-Evans rearrangement      1455
Alcohols, allylic coupling with Grignard reagents      545
Alcohols, allylic from aldehydes and allylsilanes      1211
Alcohols, allylic from alkene snlfoxides      1455
Alcohols, allylic from epoxides      1329
Alcohols, allylic reduction, reagents for      1009
Alcoholysis of acyl halides      482
Alcoholysis of amides      488
Alcoholysis of anhydrides      483
Alcoholysis of epoxides      481
Alcoholysis of esters      486
Alcoholysis of lactones      487
Aldehydes acylation of      1245
Aldehydes addition of boranes      1210
Aldehydes addition to alkenes      1033
Aldehydes and Benedict’s solution      917
Aldehydes and Fehling’s solution      917
Aldehydes and Gomberg-Bachmann pinacol synthesis      1560
Aldehydes and hydroxyalkylation of aromatic rings      719
Aldehydes and radical cyclization      1244
Aldehydes and the Barbier reaction      1205
Aldehydes and the Bouveault-Blanc reaction      1199
Aldehydes and the Cannizzaro reaction      1200 1564
Aldehydes and the Claisen reaction      1224
Aldehydes and the Darzen’s glycidic ester condensation      1230
Aldehydes and the Eschweiler-Clarke reaction      1188
Aldehydes and the Fischer indole synthesis      1453
Aldehydes and the Knoevenagel reaction      1225—1228
Aldehydes and the Leuckart reaction      1188
Aldehydes and the Meerwein-Ponndorf-Verley reduction      1199
Aldehydes and the Passerini reaction      1252
Aldehydes and the Paterno-Bchi reaction      1249
Aldehydes and the Perkin reaction      1229
Aldehydes and the Sonn-Mueller method      534
Aldehydes and the Wallach reaction      1188
Aldehydes by Hofmann rearrangement      1645
Aldehydes by hydrolysis of imines      552
Aldehydes by McFadyen — Stevens reduction      534
Aldehydes by Oppenauer oxidation      1516
Aldehydes by pinacol rearrangement      1645
Aldehydes by reduction of amides      1550
Aldehydes by Stephen reduction      1204
Aldehydes by Swern oxidation      1516
Aldehydes by the Barton reaction      1463 645
Aldehydes by the Dess-martin periodinane      1516
Aldehydes by the Etard reaction      1646
Aldehydes by the Gatterman reaction      1645
Aldehydes by the Krohnke reaction      1536
Aldehydes by the Meyers synthesis      558
Aldehydes by the Nef reaction      1178 1645
Aldehydes by the Oppenauer oxidation      1199
Aldehydes by the oxo process      1645
Aldehydes by the Pummerer rearrangement      1566
Aldehydes by the Reimer — Tiemann reaction      1645
Aldehydes by the Rosenmund reduction      532
Aldehydes by the Sommelet reaction      1536
Aldehydes by the Sonn — Mueller method      1204
Aldehydes by the Vilsmeier reaction      1645
Aldehydes by the Wacker process      1538
Aldehydes conversion to amides      925
Aldehydes decarbonylation      944
Aldehydes decarbonylation and radical rearrangement      1389
Aldehydes dissolving metal reductions      1199—1200
Aldehydes enolate anion of      also see “Enolate anions”
Aldehydes from $\alpha$-halo amides and NaOBr      1645
Aldehydes from $\alpha$-hydroxy amides and NaOBr      1645
Aldehydes from $\beta$-hydroxy alkenes      1645
Aldehydes from $\gamma$-amino halides      1645
Aldehydes from $\gamma$-hydroxy halides      1645
Aldehydes from acid derivatives      1644
Aldehydes from activated methyl groups      1646
Aldehydes from acyl halides      532 533
Aldehydes from acyl sulfonylhydrazides      534
Aldehydes from alcohols      1514—1517 1645
Aldehydes from aldehydes      1401 1644 1645
Aldehydes from alkanes      1645
Aldehydes from alkyl halides      562 1535 1644 1646
Aldehydes from allylic alcohols, arylation of      1645
Aldehydes from amides      533
Aldehydes from amines      1646
Aldehydes from anhydrides      533
Aldehydes from aromatic compounds      1645
Aldehydes from aryl acetic acids      1645
Aldehydes from aryl iodides      1645
Aldehydes from aryl nitro compounds      1645
Aldehydes from arylmethanes      1646
Aldehydes from boranes      1423 1644 1645
Aldehydes from carboxylic acid salts      1644
Aldehydes from carboxylic acids, reagents for      532 533
Aldehydes from dialkylformamides      568
Aldehydes from diazo aldehydes      1644
Aldehydes from diazonium salts      1645
Aldehydes from dithianes      1644
Aldehydes from enol ethers      1329
Aldehydes from epoxides      1398
Aldehydes from esters      1646
Aldehydes from formamides      1644—1645
Aldehydes from formates      1644
Aldehydes from formic acid      1644
Aldehydes from glycidic acids      809 1645
Aldehydes from Grignard reagents      801
Aldehydes from homologation of aldehydes      1645
Aldehydes from hydration of acetylene      1645
Aldehydes from hydroformylation of alkenes      1645
Aldehydes from hydrolysis of $\alpha$-acetoxy sulfides      1646
Aldehydes from hydrolysis of acetals      1644
Aldehydes from hydrolysis of C=N compounds      1645
Aldehydes from hydrolysis of enol esters      1644
Aldehydes from hydrolysis of enol ethers      1644
Aldehydes from hydrolysis of gem-dihalides      1644
Aldehydes from hydrolysis of hydrazones      1645
Aldehydes from hydrolysis of imines      1645
Aldehydes from hydrolysis of metalated aldimines      1645
Aldehydes from hydrolysis of oximes      1645
Aldehydes from hydrolysis of primary nitro compounds      1645
Aldehydes from hydrolysis of thioacetals      1644
Aldehydes from hydrolysis of unsaturated boranes      1645
Aldehydes from hydroperoxides      1645
Aldehydes from imines      532 1177 1644
Aldehydes from methyl groups      1463
Aldehydes from nitrites      1204 1645
Aldehydes from nitro compounds      1178 1537 1646
Aldehydes from organolithium reagents      801
Aldehydes from organometallic compounds      1645
Aldehydes from oxazines      1644
Aldehydes from oximes      1463 1645
Aldehydes from rearrangement of ally lie ethers      1645
Aldehydes from rearrangement of allylic vinylic ethers      1645
Aldehydes from rearrangement of diols      1645
Aldehydes from Reissert compounds      533
Aldehydes from sulfoxides      1566
Aldehydes from thiazoles      559
Aldehydes from thioaldehydes      1185
Aldehydes from thioesters      533
Aldehydes from unsaturated aldehydes      1645
Aldehydes from vinyl ethers      1645
Aldehydes from-1,2-diols      1645
Aldehydes from-1,3-diols      1645
Aldehydes fromalkenes      1037 1522 1525—1526 1537—1538 1645 1646
Aldehydes fromdiols      1519—1521 1645
Aldehydes fromketones      1645
Aldehydes halo, from aldehydes      775
Aldehydes halogenation, mechanism of      776
Aldehydes homologation of      1407
Aldehydes hydrogenation of      1198
Aldehydes hydroxy      see “Hydroxy Aldehydes”
Aldehydes in the Mannich reaction      1189
Aldehydes in the Mukaiyama aldol reaction      1223
Aldehydes keto-enol tautomerism      774
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