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| Ïîèñê ïî óêàçàòåëÿì |
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| Cordell G.A. (ed.) — The Alkaloids Vol. 55 |
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| Ïðåäìåòíûé óêàçàòåëü |
17-O-Deacetyl-12-methoxyvinorine structure 27
17-O-Deacetyl-21-deoxy-12-methoxyvomilenine 6
19,20-Dihydrovomilenine  data 72
19,20-Dihydrovomilenine  and mass spectral data 54
19,20-Dihydrovomilenine plant origin 12
19,20-Dihydrovomilenine structure 32
19-Hydroxy-19,20-dihydrovincamajine and mass spectral data 56
19-Hydroxy-19,20-dihydrovincamajine plant origin 14
19-Hydroxy-19,20-dihydrovincamajine structure 33
2-DeshydronortetraphylIicine 9
21-Acetyl-19,20-dihydrovomilenine and mass spectral data 56
21-Acetyl-19,20-dihydrovomilenine plant origin 14
21-Acetyl-19,20-dihydrovomilenine structure 34
21-Deoxyvomilenine 9
3-Butyl-5-propylindolizidines 165
4'-Hydroxy-3',5'-dimethoxybenzoylvincamajine and mass spectral data 60
4'-Hydroxy-3',5'-dimethoxybenzoylvincamajine plant origin 16
4'-Hydroxy-3',5'-dimethoxybenzoylvincamajine structure 37
4,6-Dialkylquinolizidine alkaloid 195C 175
5-Alkylindolizidine alkaloids 177—186
6,7-Diepicastanospermine 138
A58365A 105—108
A58365B 105—108
Ajmalidine group, mass spectrometry 67—68
Ajmaline alkaloids 65—66 70—78
Ajmaline alkaloids 47—65
Ajmaline alkaloids biogenesis 44—46
Ajmaline alkaloids biosynthesis 44—46
Ajmaline alkaloids derivatives 2
Ajmaline alkaloids early reviews 1—2
Ajmaline alkaloids mass spectrometry 47—64 66—69
Ajmaline alkaloids pharmacology 79
Ajmaline alkaloids plant origins 3—18
Ajmaline alkaloids ring system 2
Ajmaline alkaloids structures 2
Ajmaline group 66—67
Ajmaline in (-)-20-hydroxydihydrorankinidine synthesis 43
Ajmaline, Masamune synthesis 19
Ajmaline, Mashimo synthesis 19—21
Ajmaline, Sato synthesis 19—21
Ajmaline, transformation into raumacline 43
Ajmaline, van Tamelen synthesis 22—24
Allopumiliotoxins 203—210
Alstonia 9—18
Amphibians 1,4-disubstituted quinolizidine alkaloids 194—203
Amphibians 3,5-disubstituted indolizidine alkaloids 187—193
Amphibians 5,8-disubstituted indolizidine alkaloids 194—203
Amphibians 5-alkylindolizidine alkaloids 177—186
Amphibians allopumiliotoxins 203—210
Amphibians homopumiliotoxins 203—210
Amphibians indolizidine alkaloids 175—177
Amphibians pumiliotoxins 203—210
Amphibians quinolizidine alkaloids 175—177
Anti-inflammatory effects 142
Antitumor agents 142
Ants indolizidine alkaloids 165—174
Ants quinolizidine alkaloids 165—172
Apocynaceae 3—18
Aspidosperma 6 12
Astragalus 117
Astragalus polycanthus 146
Beaver indolizidine 236
Biogenesis, ajmaline alkaloids 44—46
Biomimetic semisynthesis, alstomacroline and alstonisidine 24—25
Biosynthesis ajmaline alkaloids 44—46
Biosynthesis cyclizidine 100—102
Biosynthesis swainsonine 118—119
Biotechnology, swainsonine 118—119
Bongardia chrysogonum, (+)-17-desoxycis-lamprolobine 153
Cabucala, ajmaline alkaloids 12—13
Cancer, swainsonine chemotherapy 130
Castanospermine biological activity 140—142
Castanospermine chemical transformation 139
Castanospermine isolation 130—131
Castanospermine structure 131
Castanospermine synthesis 131—138
Castanospermine-related alkaloids 130—142
Castanospermum australe, castanospermine 130—131
Cell cultures, swainsonine effects 129
Chemical transformation ajmaline into raumacline 43
Chemical transformation castanospermine 139
Chemical transformation vomilenines into perakines 42—43
Chemotherapy, with swainsonine 130
Clathyrimines 231
Clavelina picta, alkaloid 217
Clavepictine A 218—219
Clavepictine B 218—219
Comins dihydropyridone method 163
Cook synthesis, (+)-ajmaline 21—22
Cyclizidine 100—102
D-Glucopyranosides 139
Dehydroepilupinine 149
Dihydrolusitanine 152
Dihydronorpurpeline and mass spectral data 49
Dihydronorpurpeline plant origin 6
Dihydronorpurpeline structure 28
Elaeocarpus, indolizidine alkaloids 143
Endolobine and mass spectral data 48
Endolobine plant origin 5
Endolobine structure 27
Epilupinine esters 150
Epimyrtine 159—161
Esters, swainsonine-based 130
Ficuseptine 229
Fritillaria maximowiczii 147
Fungal alkaloids 94—99
Glucosidase 140—141
Glycosidase 129
Halichlorine 212—213
Halichondria okadai, halichlorine 212
Herpes simplex virus type 1, castanospermine effects 141
Herpes simplex virus type 2, castanospermine effects 141
Homopumiliotoxins 203—210
Human immunodeficiency virus type 1, castanospermine effects 141
Hydroxylated indolizidine alkaloids 1,2-dihydroxyindolizidines 112—117
Hydroxylated indolizidine alkaloids 1-hydroxyindolizidines 109—112
Hydroxylated indolizidine alkaloids swainsonine and related compounds 117—130
Immunomodulatory effects, swainsonine 128—129
Immunosuppression, by castanospermine 142
Indolizidin-3-one 178 181—182
Indolizidine 167B 178—183
Indolizidine 195B 187—188
Indolizidine 209B 196—198
Indolizidine 209D 183—185
Indolizidine 223AB 187 190—193
Indolizidine alkaloids from amphibians, 3,5-disubstituted alkaloids 187—193
Indolizidine alkaloids from amphibians, 5,8-disubstituted alkaloids 194—203
Indolizidine alkaloids from amphibians, 5-alkylindolizidine alkaloids 177—186
Indolizidine alkaloids from amphibians, isolation, structure, and biological activity 175—177
Indolizidine alkaloids from ants 165—172 173—174
Indolizidine alkaloids from Astragalus polycanthus 146
Indolizidine alkaloids from Elaeocarpus 143
Indolizidine alkaloids from Polygonatum sibiricum 146
Indolizidine alkaloids from Prosopis 144—146
Indolizidine alkaloids from tunicates 217—219
Indolizidinone 143
Indolizomycin 102—104
Ipalbidine isolation 221—222
Ipalbidine synthesis 223—224
Ipalbidinium 222
Ipalbine 221—222
| Ipomoea alba, ipalbidine and ipalbine 221—222
Isoajmaline Mashimo synthesis 19
Isoajmaline Sato synthesis 19
Isoipomine 222
Isosaraines 214—216
Julandine 229—230
Julifloricine 144—145
Juliflorinine 145—146
Juliprosine 144
Juliprosinene 145—146
Juliprosopine 144
L-Proline, to (-)-8a-epidendroprimine 147
Lasubines 231—237
Lentiginosine 112—117
Lipoprotein lipase 141
Louludinium chloride 211
Lupine alkaloids epilupinine 153—155
Lupine alkaloids epimyrtine 159—161
Lupine alkaloids isolation and structure 148—153
Lupine alkaloids lupinine 153—155
Lupine alkaloids myrtine 159—161
Lupine alkaloids tashiromine 156—158
Lupinine 153—155
Lupinus hirsutus 148
Lyngbya gracilis, louludinium chloride 211
Lythraceous alkaloids, biosynthetic studies 231—237
Maackia amurensis, (+)- -hydroxymamanine 153
Maackia hupehensis, (+)-hupeol 148
Majdinine, plant origin 14
Majorinine and mass spectral data 55
Majorinine plant origin 14
Majorinine structure 33
Masamune synthesis, ajmaline 19
Mashimo synthesis ajmaline 19—21
Mashimo synthesis isoajmaline 19
Mass spectrometry, ajmaline alkaloids 47—64 66—69
Melodinus, ajmaline alkaloids 6
Metarhizium anisopliae, swainsonine 117
Microbial alkaloids A58365A and A58365B 105—108
Microbial alkaloids cyclizidine 100—102
Microbial alkaloids indolizomycin 102—104
Moloney murine leukemia virus 141
Mucor javanicus, castanospermine effects 140
Myrmicaria eumenoides, indolizidine alkaloids 166
Myrtine 159—161
Newcastle disease virus, castanospermine effects 141
Normitoridine and mass spectral data 48
Normitoridine plant origin 5
Normitoridine structure 26
Norrauvomitine and mass spectral data 59
Norrauvomitine plant origin 16
Norrauvomitine structure 36
Nortetraphyllicine and mass spectral data 47
Nortetraphyllicine plant origin 4
Nortetraphyllicine structure 26
Norvincamajine N(1)-tri-O-methylgallate 17
Nuclear magnetic resonance  , ajmaline alkaloides 65—66 70—78
Nuclear magnetic resonance  , ajmaline alkaloids 47—65
Nuphar indolizidine 236
Oxidation, vincamajine to voachalotinal 44
Oxytropis, swainsonine 117
Perakines, from vomilenine transformation 42—43
Petrosins 214—216
Pharmacokinetics, swainsonine 129—130
Pharmacology, ajmaline alkaloids 79
Plumerinine 162
Polycanthisine 146
Polygonatum sibiricum, indolizidine alkaloids 146
Poranthera corymbosa, alkaloids 162—164
Porantherilidine 162—163
Prosopis juliflora, indolizidine alkaloids 144—146
Pumiliotoxin 251D 204
Pumiliotoxin 307A 205
Pumiliotoxins 203—210
Quebrachidine group, mass spectrometry 69
Quinolizidine alkaloids from amphibians, 1,4-disubstituted alkaloids 194—203
Quinolizidine alkaloids from amphibians, isolation, structure, and biological activity 175—177
Quinolizidine alkaloids from ants 165—172
Raucaffriline and mass spectral data 53
Raucaffriline plant origin 11
Raucaffriline structure 31
Raucaffrine 10
Raugalline 6
Raumacline, from ajmaline transformation 43
Rauscher murine leukemia virus, castanospermine effects 141
Rauvolfia, ajmaline alkaloids 4—17
Rauwolfine 6
Rhazya, ajmaline alkaloids 10
Rhizoctonia leguminicola, slaframine 94—99
Rhizoctonia leguminicola, swainsonine 117
Saraines 214—216
Sato synthesis, ajmaline 19—21
Sato synthesis, isoajmaline 19
Secophenanthroindolizidine alkaloids 225—228
Semperfiorine 4
Septicine 225—228
Serpinine 4
Simian immunodeficiency virus, castanospermine effects 141
Slaframine 94—99
Stellettamides 211—212
Streptomyces A58365A and A58356B 105—108
Streptomyces cyclizidine 100—102
Streptomyces indolizomycin 102—104
Swainsona, swainsonine 117
Swainsonine biological activity 127—130
Swainsonine biosynthesis 118—119
Swainsonine biotechnology 118—119
Swainsonine distribution 118
Swainsonine isolation 117
Swainsonine structural studies 118
Swainsonine synthesis 119—127
Swainsonine-related alkaloids 117—130
Tabernaemontana, ajmaline alkaloids 12
Tashiromine source 152
Tashiromine synthesis 156—158
Therapeutic agents D-glucopyranosides 139
Therapeutic agents with swainsonine 129—130
Tonduzia longifolia, ajmaline alkaloids 8
Tonduzia, ajmaline alkaloids 13 18
Toxicology, swainsonine 128
Transformation ajmaline into raumacline 43
Transformation castanospermine 139
Transformation vomilenines into perakines 42—43
Tunicates, alkaloids 217—219
van Tamelen synthesis, ajmaline 22—24
Vinca, ajmaline alkaloids 9 10 12—15
Vincamajine 17-O-veratrate 16
Vincamajine acetate 15
Vincamajine, oxidation to voachalotinal 44
Vincamajinine and mass spectral data 55
Vincamajinine plant origin 14
Vincamajinine structure 33
Vincamajoreine data 71
Vincamajoreine and mass spectral data 51
Vincamajoreine plant origin 9
Vincamajoreine structure 30
Voacanga, ajmaline alkaloids 10
Voachalotinal, from vincamajine oxidation 44
Vomilenines, transformation into perakines 42—43
Willicourtine 16
Z-Vomilenine 11
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