Поиск подструктуры

1433349

CN1C[C@H]2CCN(c3ccc(-c4ccc(N5N=CCCC5=O)cc4)cc3)[C@H]2C1
Reaction #41261
title compound
Выход 15.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCOCC1CCC(CN(Cc2ccccc2)S(=O)(=O)NC(=O)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)CC1
Reaction #52014
title compound
Выход 73.9%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(C(F)(F)F)cc(=O)n(-c2ccc3snc(C4OCCO4)c3c2)c1=O
Reaction #77283
title compound
Выход 17.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1CCC(c2cc(-c3ccc(F)cc3C)c(N(C)C(=O)C(C)(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)cn2)=N1
Reaction #156715
title compound
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1CCC(c2cc(-c3ccc(F)cc3C)c(N(C)C(=O)C(C)(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)cn2)=N1
Reaction #156720
title compound
Выход 118.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2(c3ccccc3)CCCCC2)cc1
Reaction #157908
1-Methoxy-4-(1-phenyl-cyclohexyl)-benzene
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2(c3ccccc3)CCCCC2)cc1
Reaction #157915
1-Methoxy-4-(1-phenyl-cyclohexyl)-benzene
DOI: 10.6084/m9.figshare.5104873.v1
COCC1CC(C(=O)OC)N(C(=O)OC(C)(C)C)C1
Reaction #159165
title compound
Выход 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC1CC(C(=O)OC)N(C(=O)OC(C)(C)C)C1
Reaction #167108
title compound
Выход 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC(=O)C1CC2CN(C(=O)OC(C)(C)C)CC2C1
Reaction #305243
1-(3-(tert-butoxycarbonyl)-3-azabicyclo[3.3.0]oct-7-yl)-2-methoxy-1-ethanone
Выход 61.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)OC1CCCCC21
Reaction #325011
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)NCCOc1ccc2c(c1)C(C1(c3ccc(F)cc3)CCC1)N(/C(=N/C(=O)OCc1ccccc1)NC(=O)OCc1ccccc1)CC2
Reaction #329255
Dibenzyl [(E)-{1-[1-(4-fluorophenyl)cyclobutyl]-7-{2-[(propylsulfonyl)amino]ethoxy}-3,4-dihydroisoquinolin-2(1H)-yl}methylylidene]biscarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCC(c2ccc(I)cc2)CC1
Reaction #341593
1-ethyl-4-(4-iodophenyl)piperidine
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOCCCCCO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N1C(=O)c2ccccc2C1=O
Reaction #351104
compound 232
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1
[Ag]
Reaction #354353
silver
Выход 551.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc([Si](C)(C)C)c(F)nc1Oc1ccc(Br)cc1I
Reaction #423003
methyl 2-(4-bromo-2-iodophenoxy)-6-fluoro-5-(trimethylsilyl)nicotinate
DOI: 10.6084/m9.figshare.5104873.v1
CCc1noc(C)c1-c1[nH]c2ccccc2c1C(C)=O
Reaction #445586
2-(3-ethyl-5-methyl-4-isoxazolyl)-3-acetyl indole
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(Nc2ncnc3[nH]ccc23)cc1Cl
Reaction #484580
(3-chloro-4-fluoro-phenyl)-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-amine
Выход 93.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc2c(Nc3ccc(F)c(Cl)c3)ncnc21
Reaction #484583
(3-chloro-4-fluoro-phenyl)-(7-methyl-7H-pyrrolo(2,3-d]pyrimidin-4-yl)-amine
Выход 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC1CC(C(=O)OC)N(C(=O)OC(C)(C)C)C1
Reaction #504858
title compound
Выход 53.0%DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее