Fuhrhop J., Penzlin G. — Organic Synthesis: Concepts, Methods, Starting materials :: Электронная библиотека попечительского совета мехмата МГУ

Главная Ex Libris Книги Журналы Статьи Серии Каталог Wanted Загрузка ХудЛит Справка Поиск по индексам Поиск Форум

Авторизация

Поиск по указателям

Fuhrhop J., Penzlin G. — Organic Synthesis: Concepts, Methods, Starting materials

Обсудите книгу на научном форуме

Нашли опечатку?
Выделите ее мышкой и нажмите Ctrl+Enter

Название: Organic Synthesis: Concepts, Methods, Starting materials

Авторы: Fuhrhop J., Penzlin G.

Язык:

Рубрика: Химия/

Статус предметного указателя: Готов указатель с номерами страниц

ed2k: ed2k stats

Издание: second edition, rewise and enlarged

Год издания: 1994

Количество страниц: 432

Добавлена в каталог: 29.10.2005

Операции: Положить на полку | Скопировать ссылку для форума | Скопировать ID

Предметный указатель

$(\pm)$ -Muscone = 3-methylcyclopentadecanone      41
$K-Selectride^{\circledR}$       107
$K-Selectride^{\circledR}$ = potassium hydrotris(1-methylpropyl)borate(1-) ( $\mathrm{KBHBU^{s}_{3}}$ )      107
$KS-Selectride^{\circledR}$       107
$KS-Selectride^{\circledR}$ = potassium tris(1,2-dimethylpropyl)hydroborate(1-) ( $\mathrm{KBHSia_{3}}$ )      107
$L-Selectride^{\circledR}$       105 107 322—323 327—328
$L-Selectride^{\circledR}$ = lithium hydrotris(1-methylpropyl)borate(1-) ( $\mathrm{LiBHBu^{s}_{3}}$ )      105 107 322—323 327—328
$LS-Selectride^{\circledR}$       107
$LS-Selectride^{\circledR}$ = lithium tris(1,2-dimethylpropyl)hydroborate(1-) ( $\mathrm{LiBHSia_{3}}$ )      107
$\alpha$ -Amino acids, activation      231—241
$\alpha$ -Amino acids, chiral products from      22—23 26 61 202—203 313—314
$\alpha$ -Amino acids, pr.      178 184—185
$\alpha$ -Amino acids, protection      228—229
$\alpha$ -Amino acids, stereoselective a-alkylation      299
$\alpha$ -Amino acids, synthesis, $\mathrm{H_{2}}$ /chiral catalyst      102—103
$\alpha$ -Amino acids, synthesis, Strecker synthesis      50 301
$\alpha$ -D-Glucofuranose, 1,2:5,6-bis-O-(1-methylethylidene) (glucose diacetonide), pr.      263
$\alpha$ -D-Glucofuranose, 1,2:5,6-bis-O-(1-methylethylidene) (glucose diacetonide), syntheses starting from      267 272—273
$\alpha$ -D-Glucofuranose, 1,2:5,6-bis-O-(1-methylethylidene) (glucose diacetonide), synthesis of      267
$\alpha$ -Diazo ketones, prepn. and Wolff rearr.      337
$\alpha$ -hydroxylation of enolates      121—122
$\alpha$ -Mannopyranosyl compds., rearrangement to 2-substituted $\beta$ -glucopyranosyl fluorides      272
$\alpha$ -Pinene, (+)-(1R)- and (-)-(1S)-, chiral boranes from      108
$\alpha$ -Pinene, (+)-(1R)- and (-)-(1S)-, pr.      192
$\alpha$ -Propoxyphene, (+)-      300
$\alpha$ -Santalene      42
$\beta$ -Carbolines      292—293
$\beta$ -Carotene, synthesis      31 41
$\beta$ -Caryophyllene = [1R-(1R*,4E,9S*)]-4,11,11-trimethyl-8-methylenebicyclo[7.2.0]undec-4-ene, synthesis step      78
$\beta$ -Eliminations, C=C double bond formation by, of $\beta$ -nitro ketones      81
$\beta$ -Eliminations, C=C double bond formation by, of alcohols      138 140—141 276—277 283
$\beta$ -Eliminations, C=C double bond formation by, of alcohols, exocyclic methylene with $\mathrm{Ar_{2}S(OR)_{2}}$       282
$\beta$ -Eliminations, C=C double bond formation by, of alcohols, undesired side-reaction      274 317
$\beta$ -Eliminations, C=C double bond formation by, of ammonium salts and $\beta$ -amino ketones      57 72—73 140—141 331
$\beta$ -Eliminations, C=C double bond formation by, of epoxides to allylic alcohols      27
$\beta$ -Eliminations, C=C double bond formation by, of glycosyl halides (HX elimination)      268
$\beta$ -Eliminations, C=C double bond formation by, of halides      52 123—124 138 140 283 286 334
$\beta$ -Eliminations, C=C double bond formation by, of halides from dichloroacetyl chloride      83 276
$\beta$ -Eliminations, C=C double bond formation by, of phosphoric 2-(arylsulfonyl)ethyl esters      216—217
$\beta$ -Eliminations, C=C double bond formation by, of sulfonium salts      38 338
$\beta$ -Eliminations, C=C double bond formation by, of sulfoxides      65 86 315
$\beta$ -Eliminations, oxidative, $\mathrm{H_{2}}$ elimination = dehydrogenation      122 138—140 249 334 337 338
$\beta$ -Eliminations, oxidative, 1,2-bis-decarboxylation      80 138 142 333 337
$\beta$ -Eliminations, pyrolytic      138 140—141
$\beta$ -Eliminations, reductive, of $\beta$ -acyloxy sulfones      34
$\beta$ -Eliminations, reductive, of $\beta$ -iodo ethers      326—327
$\beta$ -Eliminations, reductive, of 1,2-dihalides with iron(0)      78
$\beta$ -Eliminations, reductive, of 1,2-dihalides with zinc      83 119 156—157
$\beta$ -Eliminations, reductive, of 1,2-diols via cyclic carbonothioates      142
$\beta$ -Eliminations, reductive, of oxiranes      156—157
$\beta$ -Eliminations, reductive, of tosylhydrazones      14 141—142
$\beta$ -Gorgonene      33
$\beta$ -Keto carboxylic acids      see “Carboxylic acids
$\beta$ -Lactam antibiotics, synthesis      32 311—315
$\beta$ -Lactams, sensitivity of      311 313 315
$\beta$ -Lactams, synthesis from $\beta$ -chloro amides      314
$\beta$ -Lactams, synthesis from $\beta$ -hydroxv amides (Mitsunohu)      161
$\beta$ -Lactams, synthesis from cyclopropanone + amine      77—78
$\beta$ -Lactams, synthesis from sulfonyl isocyanate + alkene      153
$\beta$ -Mannopyranosides, special synth. method      271
$\delta$ -Lactams by intramol. amidation      291
$\delta$ -Lactams by photocyclization      295—296
$\delta$ -Lactones, $\beta$ -vinyl-, Ireland — Claisen rearr.      87
$\delta$ -Lactones, $\beta,\gamma$ -unsaturated, $\mathrm{CO_{2}}$ extrusion      80 92 331
$\gamma$ -Lactams, $\beta$ -amino ketone + $\mathrm{ClCH_{2}COCl}$       291
$\gamma$ -Lactams, 4-oxo acid + amine      314
$\gamma$ -Lactams, nitroalkene + $a^{3}$ -synthon      65—66 112 297
$\gamma$ -Lactones      see “Carboxylic acids
$\mathrm{C_{15}}$ salt      31
$\mathrm{C_{20}}$ salt      31
(+)-DET (diethyl $L_{g}$ -tartnue), chiral auxiliary      124—125
(+)-DET (diethyl $L_{g}$ -tartnue), pr.      185
(+)-DIPT (diisopropyt $L_{g}$ -tartrate), chiral auxiliary      124—127
(+)-DIPT (diisopropyt $L_{g}$ -tartrate), Pr.      185
(+)-Disparlure, synthesis      125
(+)-DMT (dimethyl $L_{g}$ -tartrate), chiral auxiliary      126
(+)-DMT (dimethyl $L_{g}$ -tartrate), pr.      185
(-)-Limonene      see “Cyclohexene 1-methyl-4-(1-methylethenyl)-”
(4-Methoxyphenyl)mcthyl ethers      see “Protection”
(l), like-stereoproduct symbol, definition      360
(lk), like-stereoaction symbol, definition      360
(pro-R), stereosymbol, definition      359
(pro-S), stereosymbol, definition      359
(R*), relative configuration stereosymbol      360
(Re), stereoaction symbol, definition      359—360
(S*), relative configuration stereosymbol      360
(Si), stereoaction symbol, definition      359—360
(Trimethyisilyl)methyl anion      see “Magnesium ...”
(u), unlike-stereoproduct symbol, definition      360
(ul), unlike-stereoreaction symbol, definition      360
1(2H)-Naphthalenone, 3,4-dihydro- ( $\alpha$ -tetralone), 1-spiropentanellation      79
1(2H)-Pentalenone, hexahydro-, synth.      83
1,1,5,5-Pentanetetracarboxylic acid tetraester      23
1,1-Cyclobutanedicarboxylic acid, diethyl ester      23
1,1-Dicarboxylic acids      see “Propanediol acids”
1,2-Arenediol derivs., ox. ring opening      87—88
1,2-Benzenediol derivs., ozonolysis      87—88
1,2-Benziodoxol-3(1H)-one, 1,1,1-tris(acetyloxy)-1,1-dihydro- (Dess — Martin periodinane, DMP), oxidation of alcohols      134 328—329
1,2-Cyclobutanediol, 1,2-dimethyl-, synthesis      53
1,2-Cyclotetradecancdione, synthesis      54
1,2-Dicarboxylic acids, cyclic, trans-, ring expansion of      53—54
1,2-Dicarboxylic acids, ox. decarboxylation      80 142 333 337
1,2-Dicarboxylic acids, red. cyclization      53—54
1,2-Dicarboxylic acids, synth. of cyclopentane derivs. from      59 81
1,2-Difunctional compounds      50—54 120—132
1,2-Difunctional compounds, refro-synthetic analysis      201—204
1,2-Diols, conversion to oxiranes      269
1,2-Diols, conversion to oxiranes via chlorohydrin acetates      160 327—328
1,2-Diols, ox. cleavage      81—82 202 273 292
1,2-Diols, pinacol rearr. of      32
1,2-Diols, reductive $\beta$ -elimination of      142
1,2-Diols, synthesis, opening of oxiranes      117 265 282
1,2-Diols, synthesis, oxidation of alkenes      81—82 117 123 127—130 265 276—277
1,2-Diols, synthesis, oxidation of alkenes, enantioselective      129
1,2-Diols, synthesis, pinacol coupling      53
1,2-Dioxo-compounds, ox. cleavage      137
1,2-Dioxo-compounds, synthesis by $\alpha$ -oxn. of ketones      116 122 137 156
1,2-Dioxo-compounds, synthesis by oxidation of alkynes      117 132
1,2-Dioxo-compounds, synthesis by oxn. of a-hydroxy ketones      133
1,2-Dioxo-compounds, synthesis by Pummerer rearr.      51
1,2-Dioxo-compounds, synthesis via 1-cyclobutene-1,2-diol derivs.      53—54
1,2-Ethanediamine, 1,2-diphenyl- (”stien”), (R,R)- and (S,S)-, chiral auxiliaries      68—69
1,2-Ethanediol, cyclic acetals from      165—166 (see also “Protection of carbonyl groups”)
1,2-Oxaphosphetane, Wittig transition state      30
1,3,2,4-Dithiadiphosphetane, 2,4-bis(4-methoxyphenyl)- 2,4-disulfide (Lawsson-type reagent), thionation of lactones with      110—111
1,3,2-Benzodioxaborole (catecholborane)      131
1,3,2-Diazaborolidines, chiral auxiliaries      68—69
1,3,2-Dioxaphosphole, 2,2'-oxybis[4,5-dimethyl-, 2,2'-dioxide, nucleoside coupling with      219
1,3,4-Tfaiadiazoles, 2,5-dihydro-, Barton olelination via      35
1,3,4-Thiadiazolidines, Barton olelination via      35
1,3,5,2,4,6-Trithiatrisihne      see “Cyclotrisilathiane”
1,3,5,7,9,11,13,15,17-Cyclooctadecanonaene, (E,E,Z,E,E,Z,E,E,Z)-      40 100
1,3,5,7,9-Cyclodecapentaene isomers      332
1,3,5,7-Cyclooctatetraene, reactions      331—333
1,3,5-Benzenetricarboxylic acid (trimesic acid), hydrogenation      347
1,3,5-Cycloheptatrien-1-amine, N-(1-phenylethyl)-7-[(1-phenylethyl)imino]-, (R,R)- (”chiramt”), chiral organyl cuprates from      20—21
1,3,5-Cycloheptatriene, pr.      191
1,3,5-Cycloheptatriene, synthesis of derivatives      333—334
1,3,5-Cyclohexanetricarboxylic acid, 1,3,5-trimethyl-, $(1\alpha,3\alpha,5\alpha)$ -, derivs.      346—348
1,3,7,9,13,15-Cyclooctadecahexaene-5,11,17-triyne, (E,Z,E,Z,E,Z)-      40 100
1,3-Benzenediols, hydrogenation      87
1,3-Butadiene, 1,1,2,3,4,4-hexachloro, cyclobutenes and squaric acid from      78
1,3-Butadiene, 1,1,2,3,4,4-hexachloro, pr.      186
1,3-Butadiene, 2,3-dimethyl-, diene additions of      85
1,3-Butadiene, 2,3-dimethyl-, pr.      174
1,3-Butadiene, 2-methyl- (isoprene), pr.      174
1,3-Butadiene, 2-methyl- (isoprene), [2+2]cycloaddition      153
1,3-Butadiene, cyclooligomerization      41
1,3-Butadiene, diene additions of      80 81—82 85 194 334
1,3-Butadiene, pr.      174

1,3-Cyciohexadien-5-yne (”benzyne”), addition to arenes and dienes      92—93
1,3-Cyciohexadien-5-yne (”benzyne”), generation of      39 92—93
1,3-Cyciohexadien-5-yne (”benzyne”), prepn. in solid Ar matrix      78
1,3-Cyciohexadien-5-yne (”benzyne”), rearr. of thioethers with      39
1,3-Cyclobutadiene      78
1,3-Cyclobutadiene, derivatives, synthesis      329—330
1,3-Cyclohexadienes, 5,6-bis(alkylidene)- (o-quinodimechanes)      80 153—154 280—281 297
1,3-Cyclohexadienes, diene addn. of      85 92 153
1,3-Cyclohexadienes, iron complexes, coupling reactions      44
1,3-Cyclohexadienes, pr.      190
1,3-Cyclohexanediones, 2-alkyl-, Michael addition of      71
1,3-Cyclohexanediones, 2-alkyl-, Robinson anellation of      71 73 212
1,3-Cyclohexanediones, 2-alkyl-, synthesis from 1,3-benzenediol      87
1,3-Cyclopentadiene, 1,2,3,4-tetrachloro-5,5-dimethoxy-, benzo-anellation with      337
1,3-Cyclopentadiene, 5-alkylation      210
1,3-Cyclopentadiene, 5-alkylidene (fulvenes), endoperoxide      102
1,3-Cyclopentadiene, benzvalene from      330
1,3-Cyclopentadiene, diene addns. of      85 92 210 335—336
1,3-Cyclopentadiene, diene addns. of, endoperoxide ( $\mathrm{O_{2}}: h\cdot\nu$ )      276—277
1,3-Cyclopentadiene, oxidative dimerization      336
1,3-Cyclopentadiene, pr.      189
1,3-Cyclopentanediones, 2-alkyl-, steroid ring D synthon      71 73 278—280
1,3-Cyclopentanediones, 2-alkyl-, synth.      81
1,3-Dicarbonyl type compounds, carbon acidity      9—10
1,3-Dicarbonyl type compounds, dianions of      9—10 24 204 207 325—326
1,3-Dicarboxylic acids, red. cyclization of      53—54
1,3-Dienes, cyclic, oxidation to 2-ene-1,4-diols      124 276—277
1,3-Dienes, cyclic, oxidation to endo-peroxides      102 276—277
1,3-Dienes, cyclic, pr.      189—191
1,3-Dienes, cyclic, synth. via 1,2-dihalides      123—124 334
1,3-Dienes, derivs.      see “Diels — Alder type syntheses”
1,3-Dienes, masked 1,3-diese precursors, $\alpha$ -pyrones      92 331
1,3-Dienes, masked 1,3-diese precursors, $\Delta^3$ -sulfolenes      153—154
1,3-Dienes, pr.      174 182—183 185—186 189—191
1,3-Dienes, synthesis via bis(1-alkenyl)boranes      37—38
1,3-Difunctional compounds, synthesis      55—63 119—120
1,3-Dioxanes      165 268—269 321—323 326 349
1,3-Dioxo compounds, carbon acidity      9—10
1,3-Dioxo compounds, cyclic, 1,3-cyclohexanediones      87
1,3-Dioxo compounds, cyclic, 1,3-cyclopentanediones      81
1,3-Dioxo compounds, dianions of      9—10 204
1,3-Dioxo compounds, pyrrole synthesis with      150—151
1,3-Dioxo compounds, retro-aldol type cleavage of      81 88 155—156
1,3-Dioxo compounds, selective reactions with amines      148—151 248—249 306—308
1,3-Dioxo compounds, synthesis by acylation of enamines      88
1,3-Dioxo compounds, synthesis by sulfur extrusion      59—60
1,3-Dioxol-2-one, 4,5-diphenyl, “Ox”-protected prim. amines from      164
1,3-Dioxolan-4-ones, 2-alkoxy-2,5,5-trimethyl, protected alcohols      160
1,3-Dioxolane-2-thiones, red. cleavage      142
1,3-Dioxolanes      see “Protection of carbonyl groups” “Protection
1,3-Dipolar reagents      49 41 152—153
1,3-Dithiane, 2-methyl-, acetyl $d^{1}$ -synthon      22 51 52
1,3-Dithiane, 2-methyl-, synth. from acetaldehyde      22
1,3-Dithiane, formyl $d^{1}$ -synthon      17 18 198 267
1,3-Dithianes      6 8
1,3-Dithianes, hydrolysis      22 51 79 156 267 328—329
1,3-Dithianes, reductive desulfurization      109 156
1,3-Dithianes, synthesis from acidic $\mathrm{CH_{2}}$ with 1,3-propanedithiol ditosylate      79 156
1,3-Dithianes, synthesis from aldehydes      8 22 327—328
1,3-Dithiolanes, red. desulfurization      109
1,3-Oxathiolanes      165—166 (see also “Protection”)
1,3-Oxathiolanes, hydrolysis      76 165
1,3-Poylenes, synthesis of, by 1-alkyne coupling      40 155
1,3-Poylenes, synthesis of, by bromination/dehydrobromination      124
1,3-Poylenes, synthesis of, by Heck coupling      42—43
1,3-Poylenes, synthesis of, by Julia — Lythgoe olefination      34
1,3-Poylenes, synthesis of, by McMurry olefination      41
1,3-Poylenes, synthesis of, by ring opening reactions      87—88 332
1,3-Poylenes, synthesis of, by Wittig olefination      30—33 281 334
1,3-Propanediamine, monopotassium salt (K 3-aminopropylamtde, KAPA), deprotonation of amines      249—250
1,3-Propanediamine, monopotassium salt (K 3-aminopropylamtde, KAPA), deprotonation of carbonyl compounds      10
1,3-Propanediol, 2,2-dimethyl-, pr.      175
1,3-Propanediol, 2,2-dimethyl-, protection of ketones with      165
1,3-Propanediol, 2-amino-1-phenyl-, [S-(R*,R*)]-, chiral 4,5-dihydrooxazoles      22—23
1,3-Propanediol, 2-methyl-2-propyl-, pr.      175
1,3-Propanediol, 2-methyl-2-propyl-, synth. and conversion to meprobamate      302
1,3-Propanedithiol, bis(4-methylbenzenesulfonate) ester, 1,3-dithianes from acidic $\mathrm{CH_{2}}$ groups      79 156
1,3-Propanedithiol, preparation of 1,3-dithianes from      8 17 22 328
1,3-PropanediyI, 2-methylene-, e-synthon      84
1,4,10,13-Tetraoxy-7,16-diazacyclooctadecane      247
1,4,2-Dioxazoles      153
1,4,7,10,13,16-hexaoxacyclooctadecane (18-crown-6), phase transfer catalyst      355
1,4-Cycloheptanedione, 2,6,6-trimethyl-, reductive intramolecular coupling      53
1,4-Cycloheptanedione, 2,6,6-trimethyl-, synthesis      76
1,4-Cyclohexadiene-1,2-dicarbonitrile, 4,5-dichloro-3,6-dioxo- (2,3-dichloro-5,6-dicyano-p-quinone, DDQ), oxidations with, of (4-methoxyphenyl)methyl (= MPM = PMB) ethers      157 325 326 329
1,4-Cyclohexadiene-1,2-dicarbonitrile, 4,5-dichloro-3,6-dioxo- (2,3-dichloro-5,6-dicyano-p-quinone, DDQ), oxidations with, of alcohols      133 135 334
1,4-Cyclohexadiene-1,2-dicarbonitrile, 4,5-dichloro-3,6-dioxo- (2,3-dichloro-5,6-dicyano-p-quinone, DDQ), oxidations with, of ketones ( $\alpha,\beta$ -dehydrogenation)      139—140
1,4-Cyclohexadiene-1,2-dicarbonitrile, 4,5-dichloro-3,6-dioxo- (2,3-dichloro-5,6-dicyano-p-quinone, DDQ), oxidations with, of partially hydrogenated arenes      338
1,4-Cyclohexadiene-1,2-dicarbonitrile, 4,5-dichloro-3,6-dioxo- (2,3-dichloro-5,6-dicyano-p-quinone, DDQ), oxidations with, of porphyrinogens      251 253
1,4-Cyclohexadiens, isomerization and diene addition of      85
1,4-Cyclohexadiens, oxidative ring opening of      87—88 206
1,4-Cyclohexadiens, synthesis by Birch reduction of arenes      87 97 103—104
1,4-Cyclohexadiens, synthesis by diene addn. to alkynes      194 209—210 334 335—337
1,4-Dicarboxylic acids, cyclopentane derivs. from      3 55 59 82—83
1,4-Dicarboxylic acids, synthesis by ox. opening, from 1, 2-arenediol derivs.      87—88
1,4-Dicarboxylic acids, synthesis by ox. opening, from cyclohexanones      82 137
1,4-Difunctional compounds, synthesis      63—71 76—77 79 90 123—124
1,4-Dioxo compounds, 2-cyclopenten-1-ones from      69 79
1,4-Dioxo compounds, heterocycles from      149
1,4-Dioxo compounds, synthesis of      63 65—66 69 79
1,4-Epoxynaphthalene, 1,4-dihydro-      93
1,4-Naphthalenedione, 5-hydroxy- (juglone), tetracyclines from      318
1,4:5,8-Dimethanonaphthalene, 1,2,3,4,10,10-hexachloro-1,4,4a,5,8,8a-hexahydro-, $(1\alpha,4\alpha,4\alpha\beta,5\beta,8\beta,8\alphap\beta)$ - (isodrin), pagodane and dodecahedrane from      336—337
1,4:5,8-Dimethanonaphthalene, 1,2,3,4,10,10-hexachloro-1,4,4a,5,8,8a-hexahydro-, $(1\alpha,4\alpha,4\alpha\beta,5\beta,8\beta,8\alphap\beta)$ - (isodrin), pr.      192
1,4a(2H)-Naphthalenediol, octahydro-, isomers, fragmentation      89
1,5-Cyclooctadiene, 9-BBN from      47—48
1,5-Cyclooctadiene, oxidative opening      88
1,5-Cyclooctadiene, pr.      191
1,5-Diazabicyclo[4.3.0]non-5-ene = 2,3,4,6,7,8-hexahydropyrrolo[1,2-a]pyrimidine (DBN), HBr elimination with      334
1,5-Dienes      see “Terpenes open-chain”
1,5-Dienes, acid-catd. cyclization of      90—92 279—280
1,5-Dienes, synth. by allyl coupling      39 41—42
1,5-Difunctional compounds, synthesis and reactions      71—74 90
1,5-Dioxo compounds, cyclohexenones from      71—73
1,5-Dioxo compounds, reductive cyclization of      41
1,5-Dioxo compounds, synthesis of      71—73
1,5-Heptadien-4-ol, 3,3,6-trimethyl-, synth.      45
1,5-Hexadiyne, 3-alkylation of      281
1,5-Hexadiyne, ox. cyclooligomerization of      40
1,5-Hexadiyne, [2+2+2]cyclotrimerizations with      80 281
1,5-Polyenes      see “Terpenes open-chain”
1,6-Cyclodecadiene, 1-methyl-, (E,E)-      90
1,6-Dicarbonyl type compounds, synthesis      81—82 87—88
1,6-Difunctional compounds, synthesis and reactions      81—83 87—92 136—137 206
1,6-Dioxo compounds, synthesis of      87—88 136—137
1,7,13,19-Cyclotetracosatetraen-3,5,9,11,15,17,21,31-octayne, (all-Z)-, synthesis      155
1-Alken-4-yn-3-ols      303
1-Alkynes, 1-alkoxy-hydration      64—65 325 327—328
1-Alkynes, 1-halo-, coupling with 1-alkynes      40
1-Alkynes, 1-halo-, hydroboration and coupling      37—38
1-Alkynes, acidity      5
1-Alkynes, addition to carbon dioxide      64
1-Alkynes, addition to carbonyl groups      52 62—63 278 303
1-Alkynes, addition to carbonyl groups, 2-alkyn-1-ol adducts, pr.      174 182
1-Alkynes, addition to iminium ions      57
1-Alkynes, addition to iminium ions, 2-alkyn-1-amine adducts, pr.      177
1-Alkynes, addition to oxiranes      64—65 321
1-Alkynes, hydration to aldehydes      131
1-Alkynes, hydrostannylation with $\mathrm{CuSnMe_{3}}$       321
1-Alkynes, metalation      5
1-Alkynes, metalation with Cu      57
1-Alkynes, metalation with Li or Na      52 64—65
1-Alkynes, oxidative coupling      40
1-Alkynes, synthesis, ethynylation of haloalkanes      64
1-Alkynes, synthesis, ethynylation of oxiranes      64 321
1-Alkynes, synthesis, methylidynation of aldehydes      325
1-Azabicyclo[1.1.0]butanes      154
1-Azabicyclo[2.2.2]octane derivs.      309
1-Azabicyclo[2.2.2]octane derivs., pr.      290
1-Azafulvenes      254

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15

О проекте