key: cord-0039823-ajrhgzjc authors: nan title: Cumulative general subject index: Volumes 1–20 date: 2007-09-02 journal: nan DOI: 10.1016/s1572-5995(97)80045-2 sha: 885f5ab99279c96c5a07bad30081daacfd25a372 doc_id: 39823 cord_uid: ajrhgzjc nan a-Amino ketones 2-amino alcohol by 12:411,414 reduction of 12:411,414 a-Amino ketones steroid-pyrazine dimers via 18:885-887 Amino sugar antibiotics 12:411 Amino sugars of anthracyclinones 4:350 synthesis from amino acids 4:111-156 synthesis from glycine 4:115-118 synthesis of 13:190-207 4-Amino-r',6"-anhydro-2",3",2',3',6',2,3-hept-0benzyl-4,6-dideoxy-p-maltotriose 10:508,509 2-Amino-l ,3-azulenedicarboxylate 14:339 2-Amino-2,3-di-deoxyhexoses 14:145 2-Amino-2,5,6-trideoxy-5-phosphinyl-L-galactopyranoses synthesis of 6:369 Ni ( methyl-5a-cholestan-6-one 18:512 2,13-Dihydroxy-3,l 1-epoxy APO 13:522 (/?)-2,4-Dihydroxy-3,3-dimethyl-butanoic acid 10:442, 10:443 5,3-Dihydroxy-3,6,7,4*,5'-pentamethoxyflavone 5:757 1,5-Dihydroxy-3-methoxy-10-methylacridin-9-one 13:348,350 1,2-Dihydroxy-3-pentadecyl benzene 9:314,318,343 6,8-Dihyciroxy-3-undecyl-3,4-dihydroisocoumarin 15:386 3p,20^-Dihydroxy-30-novolenan-12-en-28-oic acid 7:139,140 3,6-Dihydroxy-4,5,7-trimethylmellein 15:385 2,6-Dihydroxy-4-methoxyacetophenone 4:386,387 3,6-Dihydroxy-5,7-dimethylmellein 15:385 1,3-Dihydroxy-5-alkylbenzenes 9:320,321 l,3-Dihydroxy-5-heneicosyl benzenes 9:343 l,3-Dihydroxy-5-hexyl-2-propyl benezene 9:322 l,3-Dihydroxy-5-nonadecyl benzene 9:343 l,3-Dihydroxy-5-pentyl benzene (olivetol) 9:344 l,3-Dihydroxy-5-tridecyl benzene 9:344 1,3-dihydroxy-5-tridecyl benzene from 9:344 3p,6a-Dihydroxy-5a-pregn-9(l l)-en-20-one (asterone) 7:156,157 3p,6a-Dihydroxy-5a-pregn-9 ( ( 1:124,129-136,141-143,145,147,149 1 -(a-Hydroxyaikyl)-1,2,3,4-tetrahydroisoquinolines 12:448 1 -(a-Hydroxyalkyl)-1,2,3,4 ( TaridinA a-amylases inhibitor of 10:517 amylo-a-1,4-a-1,6-glucosidase 10:517 from Streptomyces dimorphogenes 10:517 11,12,13-Tri-«or-3,4-cuauthemone 9:66,69 Tri-«or-sesquiterpene 9:66 3,4,6-Tri Sigmatropic rearrangement 4:333 Smenospongia aurea 5:437 8-epichromazonaral from Smenospongine antimicrobial activity of 5:434,435 cytotoxic activity of 5:435 Smenospongorine 5:431 Smilagenin 7:138 ^om Echinophora lamellosa 7:136 Smith degradation 1:436,439subunit Smith's degradation Smodingium argutum 9:318 Smooth muscle Na^/H^ antiporter system 12:390 SNAr reaction 20:410 SN'-process 11:323 intramolecular Sphingadienine 1:681 Sphingofiingins antitumor activity of 17:17 Spiciformin 7:211,231 Spider mite hatching inhibitor 1:702 Spilanthes alba 10:152 Spin quantum number 9:110 of^^O 9:110 of"S 9:110 of^^Se 9:110 of^^^Te 9:110 Spin trapping experiments 9:573 Spinaceamin 15:328 Spinacetin 7:228 Spinasterol palmitate ester Spiniferin-1 from Pleraplysilla spinifera 6:72 (±)-Spiniferin-l by intramolecular cyclopropanation 6:73,74 by ring expansion rearrangement 6:73,74 synthesis of 6\13>JA 19:84 Spiro-isoquinolme derivative of ring C-homoberberine analogue 99 Spiroacetal subunits White synthesis of Spirobenzylisoquinoline alkaloids 1:187-189 formation from 8,14-cycloberbines 1:198-202 from8-methoxyprotoberberinephenolbetaines Spirobncarbocyclic chamigranes from Laurencia species 6:60 synthesis 6:59 Spirobenzoquinone ftiran unit in stypolidione 6:55 synthesis of 6:55 Spirocyclic systems Spirodysin intermediate 4:676 Spkoepoxynucleosides synthesis of Spiroketals 9:530;13:60 diaxial configuration 1:476 stereoselective synthesis of Spiroketone 8:288 from ketolactam 8:287 Spirolaurenone from homogeranonitrile bromohydrin 6:64 relation to glanduliferol 6:63 synthesis of Spirostane glycosides 17:136 Spirovetivane as sesquiterpene Spirovetivane-type sesquiterpenes enantioselective synthesis of 14:546 Spizella arborea hemoglobin components of 5:837 Spizella passerina hemoglobin components of 5:837 Splicing reaction 13:261 Spongian-type diterpenes stereoselective synthesis of Spongiaquinone potassium salt 15:298 Spongiatriol Spongiidae 6:107,19:568 Spongionella species 17:12 Songistatinl 19:580 Spongouridin 5:403 Sporobolomyces odorus Sporobolomyces reseus 5:291 Sporobolomyces sp Sporogensis 6:546 Sporomia fimgi 6-methoxymellein from 15:384 Sporothrix curviconia 5:304 Sporothrix inflata 5:304 Sporothrix schenckii Sporotrichum dimorphosporum 8:349 xylanaseA 8:349 xylanaseB Sporotrichum thermophile 2:323 Sporulation 6:552 classification of fiingi by 6:546 ^-Pulegone 20:74 Sprekeliaformosissima 20:356 Sputtering of ions (SIMS) by bombardment with fast ions 5:632 Squalene 7:131 Stannoxane 1:274 Stanols Stapfinine 5:125,172,173 Stereoselective glycosidation 8:359 Stereoselective hydrogenation Stereoselective Michael addiction 13:619 Stereoselective pinacol-type rearrangement 15:509 Stereoselective reduction 10:537 mass spectrometric analysis Steryl palmitates of5a/5P-cholestanol 9 sigmatropic rearrangement 6:315 Stevens and Bisacchi synthesis oftaxodione Stevens condensation 3:463 Stevens rearrangement 6:497 Stevia rebaudiana Steviol 13-0-p-Z)-glucoside 15:18 Steviolmonoside 15:18 Stevioside 15:16 Stichlorogenol Stichoposide D from Stichopus variegatus 7:273 Stichopus chloronotus stichlorosides Aj, Bi, Ci and A2 Stichopus sp. 7:282 Stichopus variegatus 7:272,282 stichoposide D from 7:273 Stictanin 9:186 Sticticine Stigmasteryl linoleate 9:461 Stigmastanyl ferulate 47 Still procedure 13:88 Still rearrangement 13:22 Still synthesis of(±)-A^^^^^-capnellene 6:47 ofasperdiol Stoechospermol by Baeyer-Villiger oxidation 6:39 by [2+2] photocycloaddition reaction 6:39 by Wittig olefmation 6:39 enantioselective synthesis of 6:39,40 synthesis of 6:39 Stomphia coccinea 15:66 Stongylocentrotus purpuratus 9:575 Stork modification of Michael Stork's vinyl radical cyclization 12:15 Stork-Boeckmann enone Stowell's iodide 8:146 Strecker reaction 6:312 intramolecular Strecker-type reaction 10:463 Strellidimine biogenesis of 6:516,519 from Strychnos dinklagei 6:516 spectral data of 6:516,518 synthesis of 6:516 186 Streotpmyces lysosuperficus 1:417 Streptal 14:102 Streptavidin 18:919 (+)-Streptazolin Overman synthesis of Streptococcus mutans 7:69 Streptococcus pyogenes 5:601 Streptococcus sanguis 7:69 dextransucrase from Streptolic acid synthesis of Streptolydigin phosphonate tetramic acid synthesis of 14:117 NB-2025 Streptomyces amakusaensis 19:178 Streptomyces ambofaciens Streptomyces antibioticus 11:214 Streptomyces avermitilis 1:435 avermectins from 12:3 Streptomyces azureus thiostrepton from albomitomycin A from 13:433 isomitomycin A from 13:433 mitomycins A-C from 13:433 Streptomyces cattleya thienamycin from Streptomyces chrysomallus 8:102 Streptomyces cinnamonensis 11:197 Streptomyces coelicolor 5:617,618 Streptomyces collinus ansatrienin (mycotrienin) from 11:189 enoyl CoA reductase from Streptomyces distallicus 5:551 Streptomyces erythreus 13:166 Streptomyces flaveolus tirandamycin A from 14:98 tirandamycin B from Streptomyces flavogriseus 10:103 Streptomyces flavopersicus 11:216 Streptomycesfradiae 5:591 urdamycin from Streptomyces gougerotti 4:242 Streptomyces griseochromogenes 18:269 Streptomyces griseochroogenes 4:242 Streptomyces griseoflavus Streptomyces griseolavendus 15:445 Streptomyces griseolus 1:408 Streptomyces griseoplanus 10:104 Streptomyces griseus 1:514 100 from methyl 3-acetamido-2-0-acetyl-4,6-0-from (/?)-glutamic acid 12:325 synthesis of 330 from 2,3-O-isopropylidene-L-erythrose 12:330, 331 synthesis of 12:328 276 Swainsonine stereomers 12:325 Swartzia madagascariensis 7:417 Swenton's bicyclic intermediate 14:13 Swem method 19:452 Swem oxidant 6:119,120 oxidation with 6:119,120 with oxalyl chloride 8:25 Swem oxidation 1:451 134-138 of(±)-tirandamycinB 14:123-126 of(±)-vincamine 14:726 of(±)-a-bulnesene 14:364 Swem reaction 4:425 Sweroside-gentiopicroside series 6:529 Swem-Wittig protocol 19:22 Swertiajaponica 17:421 Swinfolide 5:356 Swinholide A synthesis of 18:186-190 stereostructure of 19:589 X-ray analysis Sydnone 1:343 Sylvaticin Sylvestroside I 7:443 a-Symmetric ketones asymmetrization of Sympathomimetic amines Syn elimination ofselenoxide 16:335 oftrifluroacetate 16:357 5>'«-enoate 8:140 5y«-epoxidation 16:442 iSyw-isomerization metal ion-assisted 11:220 491 of (±)-CM-l-hydroxy indolizidine 12:279 of(±)-dihydroanatoxin-A 13:494 of (±)-elacokanine C 12:289-293 of (±)-elaeokanine A 12:289 of (±)-elaeokanine A,C 13:487 of(±)-epilupmine 13:483,484 of (±)-eremophilone 15:243 of(±)-gabaculine 13:509,510 of(±)-indolyzomycin 12:301-330 of(±)-isoretronecanol 13:483,484 of(±)-mesembrine 13:492,493 of(±)-A'a of(+)-compactin 13:555-615 of(+)-hastanencine 12:472 of(+)-heliotridine 12:472-474 of (+)-isoeremolactone 8:423,425-428 of(+)-makomakine /(5)-homoproline 13:513,514 of(S)-pinanediol 11:410 of {Z)-trans-1 -hydroxy-10-vinyl-2-cyclodecene 8:196 heptitol 11:461,462 of l,5-dihydroxy-2,3-dimethoxy-lO-methylacridin-9-one 13:354,355 ,25-dihydroxy-(24/?)-fluorocholecalciferol 10:69 of la Wittig homologation 3:268,269;11:100,101 18:8;19:22;137 for fiised lactone nucleoside synthesis 4:254 in (±)-precapnelladiene synthesis 6:39 in (±)-stoechospermol synthesis 6:39 in nakafiiran-9 synthesis 6:70 in nine-carbon sugars synthesis 4:180 of amino aldehyde 16:490 of D-galacto-hexodialdopyranose 4:163,4:164 of Z)-lyxo-pentodialdofiiranoside 4:176 of heptodialdopyranose derivative 4:180 C-glycosides by 3:218-220 hydroxyl directed 1:406 57 conformational models 3:248,252 in lactone synthesis 3:252,255 in synthesis of higher-carbon sugars 4:158 ofsecondaryallylic ethers 3:249 of tertiary allylic ethers 3:251 of zirconium enolates 3:241 of a-allyloxy anions 3:248-250 stereochemical induction 84 Wittig-methylenation ofl-mannose Wolff rearrangement 19:18 ofdiazoketone 10:593-595 oxetane ring formation Kishner cyclization 1:58 Wolff-Kishner reaction Huang-Minion modification Woodchuck hepatitis virus 20:535 Woodward reaction 19:363 Woodward reagent K 6:238 Wurmbea species synthesis of 6:158 Xanthophils 6:158 Wurtz -oxazolone 12:423 of(±)-isoconcinndiol 6:26 of(+)-aristoserratine 11:296 of(+)-aristoteline 11:278 of (+)-retigeranic acid A 13:22 of (22R23,R)-22 ( 1:10,131,315,316,386,592-595,698-701,28-30,33,155-159,165,166;3:253,237,339-345,358,590, 660,718;6:115,116,119,124,126,129,229,285,286,288, 289,292,295,296,298,299,428,426,509,511-515; 8:6,7,19,23,34,162,163,165,181,322,323,388,81 ( 10:260,261,263,266,267 161,162,167,168,170-172,175,178