Teilstruktursuche

12800

Oc1ccc2c(-c3c(-c4ccccn4)nn4c3CCC4)ccnc2c1
Reaction #8363
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCSc1c(Cl)cc2c([nH]c3cnccc32)c1[N+](=O)[O-]
Reaction #40479
6-chloro-7-ethylsulfanyl-8-nitro-9H-β-carboline
Ausbeute 81.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCSc1cc(F)cc(Br)c1
Reaction #48704
1-bromo-3-fluoro-5-propylsulfanylbenzene
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Sc1cc(F)cc(C[C@H](N)[C@H](O)[C@H]2CO[C@@H](OCC(C)(CF)CF)[C@H](C)N2)c1
Reaction #48734
desired compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)CCCC12CCC(c3nc(-c4ccc(O)cc4Cl)nn3C)(CC1)CC2
Reaction #51122
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCSCCCC12CCC(C(=O)OC)(CC1)CC2
Reaction #51136
methyl 4-[3-(ethylthio)propyl]bicyclo[2.2.2]octane-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCSC(=N)N1Cc2ccccc2-c2ccccc2C1
Reaction #63436
ethyl 5,7-dihydro-6H-dibenz[c,e]azepine-6-thiocarboximidate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCSC(=N)N1Cc2ccccc2-c2ccccc2C1
Reaction #63439
dodecyl 5,7-dihydro-6H-dibenz[c,e]azepine-6-thiocarboximidate
DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)SC(=N)N1Cc2ccccc2-c2ccccc2C1
Reaction #63440
2-butyl 5,7-dihydro-6H-dibenz[c,e]azepine-6-thiocarboximidate
DOI: 10.6084/m9.figshare.5104873.v1
N#CC1=C(C#N)Sc2c(c(=O)n3n(c2=O)CCCC3)S1
Reaction #68738
5,12-dioxo-5,7,8,9,10,12-hexahydro[1,4]dithiino[2,3-d]pyridazino[1,2-a]pyridazine-2,3-dicarbonitrile
Ausbeute 38.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@@H](S)CC1C(=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70411
3α-mercaptoandrostane-6,17-dione
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Oc1cc2ncnc(Nc3cccc(Cl)c3)c2cc1O
Reaction #80310
6,7-dihydroxy-4-(3'-chloroanilino)quinazoline
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CCSc1ccc(C(=O)O)nc1
Reaction #91690
5-(ethylthio)picolinic acid
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCSc1ccc(Br)cc1Cl
Reaction #157761
title compound
Ausbeute 80.2%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2c(O)cc(O)cc2ncn1-c1ccc(O)cc1
Reaction #217515
5,7-dihydroxy-3-(4-hydroxyphenyl)-4(3H)-quinazolinone
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(O)cc2ncn(-c3ccc(O)cc3)c(=O)c12
Reaction #217517
5-ethoxy-7-hydroxy-3-(4-hydroxyphenyl) quinazoline-4-one
Ausbeute 23.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc2c(=O)[nH]nc(-c3ccc(O)cc3)c12
Reaction #309033
4-(4-hydroxyphenyl)-3-methyl-6 h-isoxazolo[3,4-d]pyridazin-7-one
Ausbeute 53.7%DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(OC2CCCCC2)cc1
Reaction #324950
title compound
Ausbeute 45.8%DOI: 10.6084/m9.figshare.5104873.v1
CCSc1cc2c(C(=O)OC)c(C)c(-c3cccc(C(F)(F)F)c3)nc2cc1OC
Reaction #332342
methyl 6-(ethylthio)-3-methyl-7-(methyloxy)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCSc1cc2c(C(=O)OC)c(C)c(-c3cccc(C(F)(F)F)c3)nc2cc1OC
Reaction #332347
methyl 6-(ethylthio)-3-methyl-7-(methyloxy)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter