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Metzger J.V. — Thiazole and Its derivatives (Part 2)
Metzger J.V. — Thiazole and Its derivatives (Part 2)



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Название: Thiazole and Its derivatives (Part 2)

Автор: Metzger J.V.

Аннотация:

General introduction to protomeric thiazoles; aminothiazoles and their derivatives; and mercaptothiazoles, hydroxythiazoles, and their derivatives


Язык: en

Рубрика: Химия/

Статус предметного указателя: Готов указатель с номерами страниц

ed2k: ed2k stats

Год издания: 1979

Количество страниц: 590

Добавлена в каталог: 21.09.2006

Операции: Положить на полку | Скопировать ссылку для форума | Скопировать ID
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Предметный указатель
$KMnO_4$, oxidation by, 2-thiazolylsulfide      415
$pK_a$, $pK_b$      18
$pK_a$, $pK_b$ and amino-imino equilibrium      19
$pK_a$, $pK_b$ and substituents effects      19 91
$pK_a$, $pK_b$ of $\Delta$-2-thiazoline-4-one, from UV experiments, from potentiometry      423
$pK_a$, $pK_b$ of $\Delta$-4-thiazoline-one      389
$pK_a$, $pK_b$ of 2-methoxy-4-methylthiazole      389
$pK_a$, $pK_b$ of 2-methylthiothiazole, in relation with nucleophilicity      405
$pK_a$, $pK_b$ of 2-thiazolyl-oxides      409
$pK_a$, $pK_b$ of acylaminothiazoles      91
$pK_a$, $pK_b$ of azothiazoles      107
$pK_a$, $pK_b$, correlation with sigma values      19
$pK_a$, $pK_b$, representative values      20
$SOCl_2$, chlorination with      77
$S_{RN_1}$ mechanism, and halothiazoles      18
$TiCl_3$, reduction by      16
$\alpha$-Chloracetamide, with acetamidothiazoles      33
$\alpha$-Haloesters, reaction with, $\Delta$-4-thiazolinc-2-thione anion      396
$\alpha$-Naphthol, coupling with      112
$\beta$-Adrenergic receptor, blocking agents      440 441
$\beta$-Chloropropionyl chloride, with 2-hydrazinothiazoles      102
$\beta$-Chloropropionyl chloride, with aminothiazoles      50
$\beta$-Ketoesters, acylation with      53
$\beta$-Ketoesters, with hydrazinothiazoles      102
$\beta$-Naphthol, coupling with      112
$\Delta$-2-Oxazoline-5-one to $\Delta$-2-thiazoline-5-one      429
$\Delta$-2-Oxazoline-5-one, cycloaddition reactivity      436
$\Delta$-2-Oxazoline-5-one, to 5-acetylthiothia-zole      417—418
$\Delta$-2-Thiazoline-4-one, $pK_a$ measurement      423
$\Delta$-2-Thiazoline-4-one, $pK_a$ measurement, from potentiometry      423
$\Delta$-2-Thiazoline-4-one, $pK_a$ measurement, from UV data      423
$\Delta$-2-Thiazoline-4-one, 1,3-dipolar cyclo additions      425 426
$\Delta$-2-Thiazoline-4-one, 1,3-dipolar cyclo additions, with dimethyl acetylene dicarboxylate      426 427
$\Delta$-2-Thiazoline-4-one, 1,3-dipolar cyclo additions, with dimethyl fumarate      425 426
$\Delta$-2-Thiazoline-4-one, 1,3-dipolar cyclo additions, with dimethyl maleate      425 426
$\Delta$-2-Thiazoline-4-one, 2-alkylthio derivatives, hydrolysis      423
$\Delta$-2-Thiazoline-4-one, 2-alkylthio derivatives, reaction with amines      424
$\Delta$-2-Thiazoline-4-one, 2-amino derivatives, reaction with secondary amines      424
$\Delta$-2-Thiazoline-4-one, 2-chloro derivatives, hydrolysis of      423
$\Delta$-2-Thiazoline-4-one, 2-chloro derivatives, reaction with amines      424
$\Delta$-2-Thiazoline-4-one, 2-methyl-5-substituted derivatives, reaction with $p-diMeNC_6H_6CHO$      425
$\Delta$-2-Thiazoline-4-one, 2-phenyl derivatives, dimers of      420 423
$\Delta$-2-Thiazoline-4-one, 2-phenyl derivatives, structure of      419
$\Delta$-2-Thiazoline-4-one, 5-benzylidene derivatives from      425
$\Delta$-2-Thiazoline-4-one, acylation      423
$\Delta$-2-Thiazoline-4-one, dimerization of 2-phenyl derivatives      423
$\Delta$-2-Thiazoline-4-one, hydrolysis, of 2-alkylthio derivatives      423 424
$\Delta$-2-Thiazoline-4-one, hydrolysis, of 2-chloro derivatives      423 424
$\Delta$-2-Thiazoline-4-one, infrared      422
$\Delta$-2-Thiazoline-4-one, methylation of      423
$\Delta$-2-Thiazoline-4-one, NMR of      422
$\Delta$-2-Thiazoline-4-one, nucleophilic reactivity at C-5, self condensation in relation with      425
$\Delta$-2-Thiazoline-4-one, nucleophilic reactivity at C-5, with aryldiazonium salts      425
$\Delta$-2-Thiazoline-4-one, nucleophilic reactivity at C-5, with arylnitroso derivatives      425
$\Delta$-2-Thiazoline-4-one, nucleophilic reactivity at C-5, with benzaldehyde      425
$\Delta$-2-Thiazoline-4-one, nucleophilic reactivity at C-5, with benzoselenazolium salts      424
$\Delta$-2-Thiazoline-4-one, nucleophilic reactivity at C-5, with benzothiazolium salts      424
$\Delta$-2-Thiazoline-4-one, nucleophilic reactivity of oxygen      423 424
$\Delta$-2-Thiazoline-4-one, preparation of, from 4-aminothiazole      421
$\Delta$-2-Thiazoline-4-one, preparation of, general      419 426
$\Delta$-2-Thiazoline-4-one, protomeric equilibrium      421
$\Delta$-2-Thiazoline-4-one, protomeric equilibrium, infrared study of      421
$\Delta$-2-Thiazoline-4-one, protomeric equilibrium, NMR study of      421
$\Delta$-2-Thiazoline-4-one, protomeric equilibrium, solvent effect on      422
$\Delta$-2-Thiazoline-4-one, stability of      420 421
$\Delta$-2-Thiazoline-4-one, syntheses, 2-alkylthio derivatives      419
$\Delta$-2-Thiazoline-4-one, syntheses, 2-aryl-derivatives      419 420
$\Delta$-2-Thiazoline-4-one, syntheses, 2-arylthio derivatives      419
$\Delta$-2-Thiazoline-4-one, table of compounds      531—535
$\Delta$-2-Thiazoline-4-one, to 2,4-thiazolinediones      423 424
$\Delta$-2-Thiazoline-4-one, ultraviolet      422
$\Delta$-2-Thiazoline-4-thione      416
$\Delta$-2-Thiazoline-5-one, 2-benzylthio(oxo)-deiivatives, ring opening of      433 434
$\Delta$-2-Thiazoline-5-one, 2-phenyl-4-substituted derivatives, ring opening      433
$\Delta$-2-Thiazoline-5-one, 4-phenylazo derivatives, rearrangement in thiazoline      435
$\Delta$-2-Thiazoline-5-one, 4-phenylazo derivatives, ring opening      434
$\Delta$-2-Thiazoline-5-one, chloration of      432
$\Delta$-2-Thiazoline-5-one, cycloadditions reactions with, alkenes      436
$\Delta$-2-Thiazoline-5-one, cycloadditions reactions with, alkynes      436
$\Delta$-2-Thiazoline-5-one, dimerization catalyzed by $I_2$      432
$\Delta$-2-Thiazoline-5-one, enolisation with NaH      431
$\Delta$-2-Thiazoline-5-one, infrared data      430
$\Delta$-2-Thiazoline-5-one, mesoionic protomeric form      430
$\Delta$-2-Thiazoline-5-one, Michael addition of, 4-phenyl-1,2,4-triazolin-3,5-dione      433
$\Delta$-2-Thiazoline-5-one, Michael addition of, diethylazodicarboxylate      433
$\Delta$-2-Thiazoline-5-one, Michael addition of, maleic anhydride      433
$\Delta$-2-Thiazoline-5-one, NMR data      430
$\Delta$-2-Thiazoline-5-one, optically active      427
$\Delta$-2-Thiazoline-5-one, preparation of      426 427
$\Delta$-2-Thiazoline-5-one, preparation of, from $\Delta$-2-oxazoline-5-one      429
$\Delta$-2-Thiazoline-5-one, preparation of, from 4-alkylidene or 4-arylidene $\Delta$-2-thiazoline-5-one      427 428
$\Delta$-2-Thiazoline-5-one, preparation of, from 5-alkoxythiazole      430
$\Delta$-2-Thiazoline-5-one, preparation of, from N-thioacyl derivatives of amino acids      426
$\Delta$-2-Thiazoline-5-one, preparation of, optically active      427
$\Delta$-2-Thiazoline-5-one, protomeric equilibrium of, infrared      430
$\Delta$-2-Thiazoline-5-one, protomeric equilibrium of, NMR      430
$\Delta$-2-Thiazoline-5-one, protomeric equilibrium of, solvent effect on      430
$\Delta$-2-Thiazoline-5-one, protomeric equilibrium of, substituent effect on      431
$\Delta$-2-Thiazoline-5-one, protomeric equilibrium of, UV      430 431
$\Delta$-2-Thiazoline-5-one, reaction with, acetyl chloride      431
$\Delta$-2-Thiazoline-5-one, reaction with, aldehyde      432
$\Delta$-2-Thiazoline-5-one, reaction with, benzoyl chloride      431
$\Delta$-2-Thiazoline-5-one, reaction with, carbamoyl chloride      431
$\Delta$-2-Thiazoline-5-one, reaction with, enamines      432 433
$\Delta$-2-Thiazoline-5-one, reaction with, isocyanate      431
$\Delta$-2-Thiazoline-5-one, reaction with, ketone      432
$\Delta$-2-Thiazoline-5-one, reaction with, thioacetic acid      417 418
$\Delta$-2-Thiazoline-5-one, ring opening, 2-benzylthio(oxo)derivatives with, $(COCl)_2$      434
$\Delta$-2-Thiazoline-5-one, ring opening, 2-benzylthio(oxo)derivatives with, amines      433
$\Delta$-2-Thiazoline-5-one, ring opening, 2-phenyl-4-substituted derivatives with, amino acids      433
$\Delta$-2-Thiazoline-5-one, ring opening, 2-phenyl-4-substituted derivatives with, hydrazine      433
$\Delta$-2-Thiazoline-5-one, ring opening, 2-phenyl-4-substituted derivatives with, peptides      433
$\Delta$-2-Thiazoline-5-one, ring opening, 4-phenylazo derivatives with amines      434
$\Delta$-2-Thiazoline-5-one, tables of compounds      526 527
$\Delta$-2-Thiazoline-5-one, transformation in triazoline derivatives      435
$\Delta$-2-Thiazoline-5-one, UV data      431
$\Delta$-2-Thiazoline-5-thione, alkylation of, reaction with unsaturated compounds      417
$\Delta$-2-Thiazoline-5-thione, preparation of, from 5-acetylthiothiazole      416
$\Delta$-2-Thiazoline-5-thione, preparation of, from 5-thiocyanato thiazoles      416
$\Delta$-2-Thiazoline-5-thione, preparation of, general      416
$\Delta$-2-Thiazoline-5-thione, table of compounds      493—496
$\Delta$-2-Thiazoline-5-thione, tautomerism of      417
$\Delta$-3-Thiazoline      86 87
$\Delta$-4-Imidazoline-2-thione (diMel-3),methylation of      391
$\Delta$-4-thiazoline-2-one      402
$\Delta$-4-Thiazoline-2-one by hydrolysis      130
$\Delta$-4-Thiazoline-2-one in bacterial culture medium      390
$\Delta$-4-Thiazoline-2-one, $pK_a$      389
$\Delta$-4-Thiazoline-2-one, acylation of      402
$\Delta$-4-Thiazoline-2-one, ambident anion, behavior in $Na/NH_3$      398
$\Delta$-4-Thiazoline-2-one, ambidentreactivity      401
$\Delta$-4-Thiazoline-2-one, charge diagram, from HMO method      390
$\Delta$-4-Thiazoline-2-one, charge diagram, from PPP method      389 390
$\Delta$-4-Thiazoline-2-one, chlorination of      402
$\Delta$-4-Thiazoline-2-one, dimerization of      403
$\Delta$-4-Thiazoline-2-one, dipole moment, in relation with protomerism      389
$\Delta$-4-Thiazoline-2-one, electrophilic reactivity, in relation with PPP calculations      390
$\Delta$-4-Thiazoline-2-one, Friedel — Crafts reactions of      402
$\Delta$-4-Thiazoline-2-one, Gattermann reaction on      402
$\Delta$-4-Thiazoline-2-one, hydrolysis of      401
$\Delta$-4-Thiazoline-2-one, infrared, in relation with protomerism      387
$\Delta$-4-Thiazoline-2-one, infrared, in relation with self association      389 390
$\Delta$-4-Thiazoline-2-one, infrared, representative data      390
$\Delta$-4-Thiazoline-2-one, iodination      402
$\Delta$-4-Thiazoline-2-one, Mannich reaction of      403
$\Delta$-4-Thiazoline-2-one, nitration of, kinetic of      402 403
$\Delta$-4-Thiazoline-2-one, nitration of, kinetic of, conformational analysis by      390
$\Delta$-4-Thiazoline-2-one, nitration of, kinetic of, in relation with protomerism      387
$\Delta$-4-Thiazoline-2-one, nitration of, kinetic of, representative data      390 385
$\Delta$-4-Thiazoline-2-one, preparation of      372—377
$\Delta$-4-Thiazoline-2-one, preparation of, by oxidation of $\Delta$-4-thiazoline-2-thione      374 397
$\Delta$-4-Thiazoline-2-one, preparation of, from 2-biomo thiazolium salts      373
$\Delta$-4-Thiazoline-2-one, preparation of, from 2-dim ethylamino thiazolium salts      373
$\Delta$-4-Thiazoline-2-one, preparation of, from 2-imino-$\Delta$-4-thiazoline      374
$\Delta$-4-Thiazoline-2-one, preparation of, from 2-thiazole sulfonic acid      375
$\Delta$-4-Thiazoline-2-one, preparation of, from 2-thiazolyldiazonium salts      375
$\Delta$-4-Thiazoline-2-one, preparation of, from 2-unsubstituted thiazolium salts      375
$\Delta$-4-Thiazoline-2-one, preparation of, from thiazolyl-2-oxide      409 410
$\Delta$-4-Thiazoline-2-one, protomeric equilibrium, dipole moment studies      389
$\Delta$-4-Thiazoline-2-one, protomeric equilibrium, general      377
$\Delta$-4-Thiazoline-2-one, protomeric equilibrium, infrared studies      387
$\Delta$-4-Thiazoline-2-one, protomeric equilibrium, relation with self association      389
$\Delta$-4-Thiazoline-2-one, protomeric equilibrium, solvent effect on      389
$\Delta$-4-Thiazoline-2-one, protomeric equilibrium, ultraviolet studies      387
$\Delta$-4-Thiazoline-2-one, reaction with, alkylating agents      401
$\Delta$-4-Thiazoline-2-one, reaction with, chlorodiethylphosphate      401
$\Delta$-4-Thiazoline-2-one, reaction with, chlorodiethylthiophosphate      401
$\Delta$-4-Thiazoline-2-one, reaction with, diazonium salts      403
$\Delta$-4-Thiazoline-2-one, reaction with, hydrazine      402
$\Delta$-4-Thiazoline-2-one, reaction with, phosphorus chloride      401
$\Delta$-4-Thiazoline-2-one, reaction with, phosphorus pentasulfide      373
$\Delta$-4-Thiazoline-2-one, reaction with, phosphoryl chloride      401
$\Delta$-4-Thiazoline-2-one, reaction with, sulfenyl chloride      403 418
$\Delta$-4-Thiazoline-2-one, reduction of, with zinc dust      402
$\Delta$-4-Thiazoline-2-one, Reimer — Tiemann reaction on      402
$\Delta$-4-Thiazoline-2-one, sel association, in relation with protomerism      377
$\Delta$-4-Thiazoline-2-one, sulfonation of      402
$\Delta$-4-Thiazoline-2-one, tables of compounds, 3,4,5-trisubstituted      520—523
$\Delta$-4-Thiazoline-2-one, tables of compounds, 3,4-disubstituted      519
$\Delta$-4-Thiazoline-2-one, tables of compounds, 3,5-disubstituted      520
$\Delta$-4-Thiazoline-2-one, tables of compounds, 3-pyrimidinylmethyl derivatives      523 524
$\Delta$-4-Thiazoline-2-one, tables of compounds, 3-substituted      518
$\Delta$-4-Thiazoline-2-one, tables of compounds, 4,5-disubstituted      515—518
$\Delta$-4-Thiazoline-2-one, tables of compounds, 4-substituted      513 514
$\Delta$-4-Thiazoline-2-one, tables of compounds, 5-substituted      513
$\Delta$-4-Thiazoline-2-one, tables of compounds, miscellaneous      524 525
$\Delta$-4-Thiazoline-2-one, to 2-imino-4-thiazolines      123
$\Delta$-4-Thiazoline-2-one, transformation in, 2-chlorothiazole      402
$\Delta$-4-Thiazoline-2-one, transformation in, 2-chlorothiazole, thiochrome      402
$\Delta$-4-Thiazoline-2-one, transformation in, 2-chlorotliiazoles      401
$\Delta$-4-Thiazoline-2-one, transformation in, 2-chlorotliiazoles, 2-thiazolyloxides      401
$\Delta$-4-Thiazoline-2-one, transformation in, 2-chlorotliiazoles, 2-unsubstituted thiazoles      402
$\Delta$-4-Thiazoline-2-one, transformation in, 2-chlorotliiazoles, N-substituted derivatives      401
$\Delta$-4-Thiazoline-2-one, ultraviolet, in relation with protomerism      387
$\Delta$-4-Thiazoline-2-one, ultraviolet, representative data      389
$\Delta$-4-Thiazoline-2-one, uses      438
$\Delta$-4-Thiazoline-2-selenone, photographic processes      370
$\Delta$-4-Thiazoline-2-selenone, properties of      370
$\Delta$-4-Thiazoline-2-selenone, silver halide emulsion      370
$\Delta$-4-Thiazoline-2-selenone, table of compounds      536
$\Delta$-4-Thiazoline-2-thione      123
$\Delta$-4-Thiazoline-2-thione, ambident anion of, charge diagram from PPP calculation      390
$\Delta$-4-Thiazoline-2-thione, ambident anion of, reactivity      394
$\Delta$-4-Thiazoline-2-thione, ambident anion of, reactivity, in Mannich reaction      394
$\Delta$-4-Thiazoline-2-thione, ambident anion of, reactivity, steric effect on      394
$\Delta$-4-Thiazoline-2-thione, ambident anion of, reactivity, with $\alpha$-haloesters      396
$\Delta$-4-Thiazoline-2-thione, ambident anion of, reactivity, with $\beta$-dimethylaminomethyl chloride      396
$\Delta$-4-Thiazoline-2-thione, ambident anion of, reactivity, with 1,4-dichloro-2-butene      396
$\Delta$-4-Thiazoline-2-thione, ambident anion of, reactivity, with 1,4-dichloro-2-butyne      396
$\Delta$-4-Thiazoline-2-thione, ambident anion of, reactivity, with 2-chloro-propionitrile      396
$\Delta$-4-Thiazoline-2-thione, ambident anion of, reactivity, with acrylonitrile      394
$\Delta$-4-Thiazoline-2-thione, ambident anion of, reactivity, with acyl chlorides      396
$\Delta$-4-Thiazoline-2-thione, ambident anion of, reactivity, with alkyl halides      396
$\Delta$-4-Thiazoline-2-thione, ambident anion of, reactivity, with aryl halides      396
$\Delta$-4-Thiazoline-2-thione, ambident anion of, reactivity, with cyanuric chloride      396
$\Delta$-4-Thiazoline-2-thione, ambident anion of, reactivity, with halogenothiazoles      396
$\Delta$-4-Thiazoline-2-thione, ambident anion of, reactivity, with lactones      396
$\Delta$-4-Thiazoline-2-thione, ambident anion of, reactivity, with methylvinylketone      394
$\Delta$-4-Thiazoline-2-thione, ambident anion of, reactivity, with N,N-dimethylthiocarbamoyl chloride      396
$\Delta$-4-Thiazoline-2-thione, ambident anion of, reactivity, with tetra-O-acetyl-D-glucopyranosyl bromide      394
$\Delta$-4-Thiazoline-2-thione, ambident anion of, reductive ring opening in $Na/NH_3$      397
$\Delta$-4-Thiazoline-2-thione, aryl derivatives, by isomerization reactions      373
$\Delta$-4-Thiazoline-2-thione, charge diagrams, CNDO      385
$\Delta$-4-Thiazoline-2-thione, charge diagrams, PPP      385 389
$\Delta$-4-Thiazoline-2-thione, circular dichroism      380
$\Delta$-4-Thiazoline-2-thione, CNDO calculations      380 385 389
$\Delta$-4-Thiazoline-2-thione, complexes with, $HgBr_2$      396
$\Delta$-4-Thiazoline-2-thione, complexes with, Ag      386
$\Delta$-4-Thiazoline-2-thione, complexes with, Cd      412
$\Delta$-4-Thiazoline-2-thione, complexes with, Cu      412 386
$\Delta$-4-Thiazoline-2-thione, complexes with, Mg      412
$\Delta$-4-Thiazoline-2-thione, complexes with, Ni, Co      412
$\Delta$-4-Thiazoline-2-thione, complexes with, Pb      412
$\Delta$-4-Thiazoline-2-thione, complexes with, transition metals      386
$\Delta$-4-Thiazoline-2-thione, complexes with, Zn      412
$\Delta$-4-Thiazoline-2-thione, conformational analysis of alkyl substituents      385
$\Delta$-4-Thiazoline-2-thione, desulfurization      393 397 399
$\Delta$-4-Thiazoline-2-thione, dipole moment, in relation with protomerism merism      379
$\Delta$-4-Thiazoline-2-thione, dynamic NMR      384—385
$\Delta$-4-Thiazoline-2-thione, from 2-immo-4-thiazolihes      126
$\Delta$-4-Thiazoline-2-thione, hetero-association of, with 4-chlorophenol      377
$\Delta$-4-Thiazoline-2-thione, hetero-association of, with DMSO      377
$\Delta$-4-Thiazoline-2-thione, infrared spectra      381
$\Delta$-4-Thiazoline-2-thione, metal salts, asgennidices      412
$\Delta$-4-Thiazoline-2-thione, metal salts, in analysis      412
$\Delta$-4-Thiazoline-2-thione, metal salts, in photographic processes      412
$\Delta$-4-Thiazoline-2-thione, metal salts, in rubber industry      412
$\Delta$-4-Thiazoline-2-thione, NMR, $^{13}C$ data      384 385 388
$\Delta$-4-Thiazoline-2-thione, NMR, barrier to rotation of alkyl substituent      384 385
$\Delta$-4-Thiazoline-2-thione, NMR, representative data      384
$\Delta$-4-Thiazoline-2-thione, oxidation of, with $N_2O_4$      393
$\Delta$-4-Thiazoline-2-thione, oxidation of, with ammonium persulfate      394 397
$\Delta$-4-Thiazoline-2-thione, oxidation of, with hydrogen peroxide      374 383 397
$\Delta$-4-Thiazoline-2-thione, oxidation of, with iodine      393
$\Delta$-4-Thiazoline-2-thione, oxidation of, with mercuric acetate      374
$\Delta$-4-Thiazoline-2-thione, oxidation of, with NaOCl in presence of amine      411
$\Delta$-4-Thiazoline-2-thione, oxidation of, with nitric acid andsodium nitrite      393
$\Delta$-4-Thiazoline-2-thione, photoelectron spectra      381
$\Delta$-4-Thiazoline-2-thione, PPP calculations      380 385 389
$\Delta$-4-Thiazoline-2-thione, preparation of, by isomcrization of 5-methylenethiazoli-dine-2-thione      372 373
$\Delta$-4-Thiazoline-2-thione, preparation of, by rearrangement of thiazolyl-2-thioethers      406
$\Delta$-4-Thiazoline-2-thione, preparation of, from $\Delta$-4-thiazoline-2-one and $P_2S_5$      373
$\Delta$-4-Thiazoline-2-thione, preparation of, from 1,3,4-thiadiazole-2-thione and alkyne      372
$\Delta$-4-Thiazoline-2-thione, preparation of, from 1,3-dithiolane and alkyne      372
$\Delta$-4-Thiazoline-2-thione, preparation of, from 1,3-dithiole-2-thione and amine      372
$\Delta$-4-Thiazoline-2-thione, preparation of, from 2-aminothiazole      370
$\Delta$-4-Thiazoline-2-thione, preparation of, from 2-benzylthiothiazolcs      405
$\Delta$-4-Thiazoline-2-thione, preparation of, from 2-bromothiazole and thiourea      370
$\Delta$-4-Thiazoline-2-thione, preparation of, from 2-iminothiazole and $CS_2$      371
$\Delta$-4-Thiazoline-2-thione, preparation of, from 2-iminothiazolium salts and $H_2S$      371
$\Delta$-4-Thiazoline-2-thione, preparation of, from 2-thiazolyldiazonium salts and potassium $\Delta$-4-Thiazoline-2-thione, preparation of, ethylxanthate or thiourea      370
$\Delta$-4-Thiazoline-2-thione, preparation of, from 2-thiocyanothiazole      370
$\Delta$-4-Thiazoline-2-thione, preparation of, from 2-unsubstituted thiazoliumsalts      375
$\Delta$-4-Thiazoline-2-thione, preparation of, from deoxybenzom and $S_8$      373
$\Delta$-4-Thiazoline-2-thione, preparation of, from dithiazolylsulfidehydrochloride      405
$\Delta$-4-Thiazoline-2-thione, preparation of, from thiazolyl-2-disulfides      412
$\Delta$-4-Thiazoline-2-thione, preparation of, propargyl amine and $CS_2$      372
$\Delta$-4-Thiazoline-2-thione, protomeric equilibrium, general      377
$\Delta$-4-Thiazoline-2-thione, protomerism, IR studies of      378
$\Delta$-4-Thiazoline-2-thione, protomerism, RMN studies of      379
$\Delta$-4-Thiazoline-2-thione, protomerism, solvent effect on      379
$\Delta$-4-Thiazoline-2-thione, protomerism, ultraviolet studies      378
$\Delta$-4-Thiazoline-2-thione, Raman spectra      381
$\Delta$-4-Thiazoline-2-thione, reaction with, alkylation agents, quantitative aspects, alcohols in $\Delta$-4-Thiazoline-2-thione, reaction with, alkylation agents, quantitative aspects, acidic medium      392
$\Delta$-4-Thiazoline-2-thione, reaction with, alkylation agents, quantitative aspects, alkenes      392
$\Delta$-4-Thiazoline-2-thione, reaction with, alkylation agents, quantitative aspects, alkyl halides      391
$\Delta$-4-Thiazoline-2-thione, reaction with, alkylation agents, quantitative aspects, dihalogenoalkanes      391. See also Nucleophilic substitution
$\Delta$-4-Thiazoline-2-thione, reaction with, mercury complexes      394
$\Delta$-4-Thiazoline-2-thione, reaction with, mercury complexes, tin complexes      394
$\Delta$-4-Thiazoline-2-thione, reactivity of, thiocarbonyl nudeophilicity      384 391—393
$\Delta$-4-Thiazoline-2-thione, rearrangement of 3-ammomethyl derivatives      400
$\Delta$-4-Thiazoline-2-thione, table of compounds, 3,4,5-trisubstituted      486—491
$\Delta$-4-Thiazoline-2-thione, table of compounds, 3,4-disubstituted      480—484
$\Delta$-4-Thiazoline-2-thione, table of compounds, 3,5-disubstituted      485
$\Delta$-4-Thiazoline-2-thione, table of compounds, 3-pyrimidinylmethyl derivatives      492
$\Delta$-4-Thiazoline-2-thione, table of compounds, 3-substituted      479 480
$\Delta$-4-Thiazoline-2-thione, table of compounds, 4,5-disubstituted      477—479
$\Delta$-4-Thiazoline-2-thione, table of compounds, 4-substituted      474 475
$\Delta$-4-Thiazoline-2-thione, table of compounds, 5-substituted      476
$\Delta$-4-Thiazoline-2-thione, thin-layer chromatography      385
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