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1430669

CC(C)(C)OC(=O)N1C(CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)C(c2cc(F)ccc2F)=CC1c1ccccc1
Reaction #61135
1-7
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(Oc3ccc(NS(=O)(=O)C(F)(F)F)cc3)c(-c3ccccc3)c(C)cc2c1
Reaction #185253
DOI: 10.1039/C8SC04228D
COc1ccc(Cn2ncc3c(N4CCN(C(=O)OC(C)(C)C)CC4)c(Br)cnc32)cc1
Reaction #191089
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=CC[C@@H]2[C@H]1[C@@]2(F)C(=O)OCC
Reaction #217679
(1R,5R,6R)-6-fluoro-bicyclo[3.1.0]hex-2-ene-2,6-dicarboxylic acid diethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2ncc3c(N4CCN(C(=O)OC(C)(C)C)CC4)c(I)cnc32)cc1
Reaction #241582
DOI: 10.1039/C8SC04228D
CC(CNS(=O)(=O)C(C)C)C1CC=C(c2ccc(C=O)cc2)CC1
Reaction #366535
title compound
Выход 26.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@]1(O)C(=O)OCc2c1cc1n(c2=O)Cc2cc3ccccc3nc2-1
Reaction #439167
camptothecin
Выход 73.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@](O)(c1ccccc1)C1CCCC1
Reaction #453596
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2ncc3c(N4CCN(C(=O)OC(C)(C)C)CC4)c(Br)cnc32)cc1
Reaction #474705
tert-butyl 4-(5-bromo-1-(4-methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-4-yl)piperazine-1-carboxylate
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2ncc3c(N4CCN(C(=O)OC(C)(C)C)CC4)c(Br)cnc32)cc1
Reaction #474738
tert-butyl 4-(5-bromo-1-(4-methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-4-yl)piperazine-1-carboxylate
Выход 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2ncc3c(N4CCN(C(=O)OC(C)(C)C)CC4)ccnc32)cc1
Reaction #474749
tert-butyl 4-(1-(4-methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-4-yl)piperazine-1-carboxylate
Выход 99.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2ncc3c(N4CCN(C(=O)OC(C)(C)C)CC4)c(I)cnc32)cc1
Reaction #474772
tert-butyl 4-(5-iodo-1-(4-methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-4-yl)piperazine-1-carboxylate
Выход 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2ncc3c(N4CCN(C(=O)OC(C)(C)C)CC4)c(Cl)cnc32)cc1
Reaction #474784
tert-butyl 4-(5-chloro-1-(4-methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-4-yl)piperazine-1-carboxylate
Выход 61.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(CO[Si](c3ccccc3)(c3ccccc3)C(C)(C)C)CC[C@]3(C)C(CC[C@@H]4[C@@]5(C)CC=C(OS(=O)(=O)C(F)(F)F)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #494074
(1R,3aS,5aR,5bR,7aR,11aR,11bR,13bR)-3a-((tert-butyldiphenylsilyloxy)methyl)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-octadecahydro-1H-cyclopenta[a]chrysen-9-yl trifluoromethanesulfonate
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1C=C(c2ccccc2C(F)(F)F)CCN1
Reaction #576850
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccccc1C1=CC(C(=O)OC(C)(C)C)NCC1
Reaction #576855
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC=C(OS(=O)(=O)C(F)(F)F)CC1
Reaction #591002
4-trifluoromethanesulfonyloxy-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)NCCC1CCC(=O)CC1
Reaction #653656
title compound
Выход 26.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C#Cc2ccc3nccn3n2)cc1
Reaction #677079
4-(imidazo[1,2-b]pyridazin-6-ylethynyl)aniline
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cccc(C#Cc2ccc3nccn3n2)c1
Reaction #677094
3-(imidazo[1,2-b]pyridazin-6-ylethynyl)aniline
DOI: 10.6084/m9.figshare.5104873.v1
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