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Taticchi A., Frinquelli F. — The Diels-Alder Reaction: Selected Practical Methods
Taticchi A., Frinquelli F. — The Diels-Alder Reaction: Selected Practical Methods



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Название: The Diels-Alder Reaction: Selected Practical Methods

Авторы: Taticchi A., Frinquelli F.

Аннотация:

The Diels-Alder reaction mechanism was first reported in 1928 and in the last 70 years has become one of the most commonly used and studied methodologies in organic chemistry. The reaction, which involves the addition of a diene to an alkene to form a six-membered ring, is particularly important in the synthesis of compounds of practical interest such as drugs, dyes, polymers, fragrances, agrochemicals and fine chemicals. The experimental procedure is very simple with generally good yields and minor side reactions. The use of organic solvents is not always necessary - an important factor when considering greener synthetic options. This book focuses on practice, describing procedures and techniques and as well as reporting on industrial applications. Graphical illustration presents the concepts in a clear and concise format, covering procedures and techniques employed to realize selective and clean syntheses based on the Diels-Alder methodology.


Язык: en

Рубрика: Химия/

Статус предметного указателя: Готов указатель с номерами страниц

ed2k: ed2k stats

Год издания: 2002

Количество страниц: 356

Добавлена в каталог: 29.03.2009

Операции: Положить на полку | Скопировать ссылку для форума | Скопировать ID
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Предметный указатель
N-alkyl maleimides      253 254t
N-allylic enamides      191 200
N-benzyl-N-methallyl acrylamide      191
N-benzylideneaniline      264
N-Bromosuccinimide      53
n-butyl acrylate      178 288
N-butylmaleimide      177
N-crotonyl oxazolidinone      133
N-ethylmaleimide      184 252 253 254t
N-methylmaleimide      7 276
N-phenyl maleimide      43 44 144—145
N-phenylsulfonylindole-3-carbaldehyde      63
N-sulphinylphosphoramidates      136
Nafion-H      189
Naphthalenes      110 212
Naphthanilides      211
Naphthols      41
Nickel catalysts      127
Nickel-cyclooctadiene      18 19t 20t
Niobium      132
Nitroalchenes, $\alpha,\beta$-unsaturated      274
Nitroalkenes      30 159
Nitrobenzene      162
Nitrocyclohexanones      30
Nitrogen heterocycles      72 149
Nitromethane      114 273—274 295
Nitrostyrene      51 237 273
Norbornadiene      18 37 126 127 291
Norbornanes      37
Norbornene      38 119 226
Norbornenones      37
Normal electron-demand Diels — Alder reactions      3 4 23 29 69 234
o-aminobenzylalcohols      67
o-benzoquinones      89
o-hydroxy thi oph thai imides      68
o-quinodimethanes      43 46 47 218
o-quinone      154 155 182 195
o-silylenol ethers      136
o-thioquinones      68
Octahydrobenzazepinones      152
Octalones      101
Orthoesters, ketals of      271
Oxasilacyclopentanes      89
Oxazaborinane      118
Oxazoborolidinone      147
Oxoenaminoketones      69
p-Benzoquinone      see “1
p-methoxybenzaldehyde      123
p-toluene-sulfonic acid      211
p-toluensulphonylisocyanate      72
Palasonin      231
Palitaxel      231
Para-chlorophenol      276—278
Pen tamethylcycl open tadiene      10
Pentacene      193
Pentahelicenes      65
Perfluorooctanonitrile      213
Phenanthrene-1,4-diones      50
Phenanthridinone      134
Phenols      32 182 281
Phenylacetylene      168
Phenylglyoxal      264
Phenylnitrocyclohexenes      51
Phenylsulfinylselenylchloride      72
Phenyltriazolinedione      73 80
Phorbols      233 234
Piperylene      24 275
Polycyclic cage compounds      80
Polymers      232 284
Porphyrin      170
Propane      284 286 287
Prosolanapyrone      181 199
Prostatin      233
Pumiliotoxin      171 257
Pyranes, synthesis of      123—125
Pyrano-[4,3-b]-pyrrole      44
Pyridazines, 3,5-disubstituted      91
Pyridines      68 79 123
Pyridones      91 234—236
Pyrimidones      91
Pyrones      90 122—123 126—128 181 199 234
Pyrrole 2, 3-quinodimethane      44
Pyruvaldehyde      258 264
Pyruvic acid      258
Quassinoids      255
Quinoline      134
Quinoline-5,8-dione      106
Quinolizidine      291
Quinone      33 88 109 176
Quinone-mono-ketals      212 241
Rare earth metals      108
Reaction medium, choice of      251
Reactivity-selectivity principle      99
Rearrangements, sigmatropic      268
Regiochemistry      10—12
Regioselectivity      36 42 72 99
S-(+)-2-methoxymethyl pyrrolidine      30
Salvia miltiorrhiza      154 195
Scandium (III) perfluorooctanesulfonate      134
Scandium triflate      108—110 120 293
Secohexaprismane      81
Selenides, allyl alkenyl      85
Selenoaldehydes      71 85
Selenoketones      85
Self-Diels — Alder reactions      148
Sesquiterpenes      77 210
Silica gel      115 133 143 146 147 161
Siloles      234
Silyl triflate      151 194
Silyloxy dienes      151 194
Silylthioaldehydes      70
Sodium dodecyl sulfate      174 177 178 282
Solanapyrones      181 199
Solvents      207 252 278 284 286
Sonochemical effect      156 195
Stereochemistry      12—15
Stereoselectivity, of cycloadditions      99
Steroids      53 212
Styrene      49—51 88 219 276
Sugar allyltins      240
Sulfinimides, $\alpha,\beta$-unsaturated      239
Sulfinylacrylate      113
Sulfolenes, thermolysis of      44
Sultones, $\alpha,\beta$-unsaturated      88
Supercritical fluids      284—289 296
Swainsonine      171 257
t-butyl methyl ether (TBME)      167
t-butylglyoxylate      215
Tanshindiol B      195
Tantalum      132
Tellurides      85
Telluroaldehydes      85
Temporary metal connection strategy      193
Terpenoids, bioactive      135
Tert-aminodienylesters      88
Tetra-n-butylammonium fluoride      16
Tetracene      193
Tetrachlorocyclopropene      32
Tetrachlorothiophene dioxide      184
Tetracyanoethylene      80
Tetrafluorobenzyne      229
Tetrahydrobenzofurans      57
Tetrahydrocarbazoles      63 64
Tetrahydrofuran      7 8 16 115 168 255 260
Tetrahydropyridines      237 239 264
Tetrahydrothiopyrans      79
Tetramethylbisdialine      65
Tetraphenylporphyrin      163 169
Thieno-o-quinodimethanes      46
Thioaldehydes      71
Thioazadienes      67
Thiochromanones      69
Thioketones      123
Thiones      68
Thiophene      40 57 229—234
Thiopyrans      69 123
Tosylimine      72
Trans, trans-2,4-hexadiene      9
Transition metal catalysts      18 114—115 126 127 128 137
Trehalose      260
Trialkylamines      281
Triazines      70 126 237
Tricarbonyl (tropone) iron      213
Triethylamine      7 8 36 56 164
Triflic acid      6 151 185 186t
Trifluoroacetic acid      149 151 270 271
Trifluoromethanesulfonic acid      see “Triflic acid”
Trifluoromethyl diethylphthalate      34
Trifluoromethylethylbenzoate      34
Trimethyl orthoformate      151
Trimethylaluminum      117
Trimethylsilylimines      67
Trimethylsilyltriflate      6 115 128
Tris-(p-bromophenyl)aminium hexachloroantimonate      9 157
Tris-(trimethylsilyl)silane      8
Tropolone      226
Tropone      32 213 226—229
Tyrosinase      182 183t
Ugi reaction      149
Vinylallenes      90
Vinylbenzofurans      57 59 60
Vinylbenzo[b]thiophenes      60
Vinylboranes      36
Vinylcyclohexene      148 154 155
Vinylethers      68 124 126 133 264
Vinylfurans      56 57 58
Vinylindole      60 62 63 64 87
Vinylnaphthalenes      49—54 219 220
Vinyloxocarbenium ions      188 199
Vinylpyrazoles      58 159
Vinylthioethers      264
Vinylthiophenes      56 58
Water      197 282 284 285
Wittig reaction      63
Woodward — Hoffmann rules      24
Ytterbium catalysts      126
Zeolites      143 146 147—148 194
Zinc chloride      223
Zinc didodecyl sulfate      177
[1,3]-sigmatropic hydrogen shifts      159
[12]-cyclacene      218
1 2 3
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