部分構造検索

CCCCC(C)O

CCCCCC(O)CCCOC(=O)c1ccccc1
Reaction #884
4-hydroxy-nonyl benzoate
DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cccc(C(=O)NC(C)c3ccc(F)cc3)c2)C1
Reaction #49248
title compound
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cccc(C(=O)NC(C)c3ccc(F)cc3)c2)C1
Reaction #49249
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCN(CC(c2ccc(Cl)c(Cl)c2)C2(O)CCCCC2)CC1
Reaction #57084
tert-butyl {1-[2-(3,4-dichlorophenyl)-2-(1-hydroxycyclohexyl)ethyl]piperidin-4-yl}carbamate
収率 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)OC1(C)CCCCC1)c1ccc(N)cc1
Reaction #62816
1-methylcyclohexyl 2-(p-aminophenyl)-propionate
収率 67.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)OC1(C)CCCCC1)c1ccc2nc(N)sc2c1
Reaction #62817
1-methylcyclohexyl 2-amino-α-methylbenzothiazole-6-acetate
収率 73.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)OC12CC3CC(CC(C3)C1)C2)c1ccc(N)cc1
Reaction #62819
1-adamantyl 2-(p-aminophenyl)propionate
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1O[C@H](COC(=O)c2ccccc2)[C@@H](O)[C@H](N=[N+]=[N-])[C@H]1OCc1ccccc1
Reaction #72435
title compound
収率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(N)(c1ccccc1)C1CCC(Oc2cc3ccnc(OCc4ccccc4)c3cc2Cl)CC1
Reaction #73483
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@@H]1[C@@H](Cc2ccc(C(F)(F)F)cc2)COC[C@H](NC(=O)c2nccc(OC)c2OCOC(=O)COCC)C(=O)O[C@H]1C
Reaction #87243
((4-methoxy-2-(((3S,7S,8R,9S)-9-methyl-2-oxo-8-propoxy-7-(4-(trifluoromethyl)benzyl)-1,5-dioxonan-3-yl)carbamoyl)pyridin-3-yl)oxy)methyl 2-ethoxyacetate
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1C[C@H](OC)CN[C@@H]1C(=O)N1CCN(c2ccccc2)CC1
Reaction #89751
methyl(2S,3S,5S)-5-methoxy-2-[(4-phenylpiperazin-1-yl)carbonyl]piperidine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H]1C[C@H](OC)CN(C(=O)OC)[C@@H]1C(=O)N1CCN(c2ccccc2)CC1
Reaction #89752
dimethyl(2S,3S,5S)-5-methoxy-2-[(4-phenylpiperazin-1-yl)carbonyl]piperidine-1,3-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CCC(=O)OCc1ccccc1)O[C@@H]1O[C@@H](C)[C@H](OC(=O)[C@H](C)CN=[N+]=[N-])C[C@H]1O
Reaction #90246
(R)-benzyl 4-(((2R,3R,5R,6S)-5-(((R)-3-azido-2-methylpropanoyl)oxy)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)pentanoate
収率 17.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CCC(=O)OCc1ccccc1)O[C@@H]1O[C@@H](C)[C@H](OC(=O)[C@H](C)CN=[N+]=[N-])C[C@H]1OC(=O)CCCCO[C@@H]1O[C@@H](C)[C@H](OCc2ccccc2)C[C@H]1OCc1ccccc1
Reaction #90247
(2R,3R,5R,6S)-5-(((R)-3-azido-2-methylpropanoyl)oxy)-2-(((R)-5-(benzyloxy)-5-oxopentan-2-yl)oxy)-6-methyltetrahydro-2H-pyran-3-yl 5-(((2R,3R,5R,6S)-3,5-bis(benzyloxy)-6-methyltetrahydro-2H-pyran-2-yl)oxy)pentanoate
収率 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1CNCC[C@H]1CC[C@H](O)c1ccnc2ccc(OC)cc12
Reaction #93499
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(=S)N[C@@]1(c2cc(Br)ccc2F)CO[C@@H](C2CC2)C[C@H]1CO)c1ccccc1
Reaction #155616
product
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(F)c([C@]23CO[C@@H](C4CC4)C[C@H]2CSC(NC(=O)c2ccccc2)=N3)c1
Reaction #155617
product
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]([C@@H]1CCCN1)[C@@H](C)C(=O)NCCc1ccccc1.Cl
Reaction #161913
(2R,3R)-3-methoxy-2-methyl-N-(2-phenylethyl)-3-[(2S)-pyrrolidin-2-yl]propanamide, hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)NCCc1ccccc1)OC)N(C)C(=O)[C@@H](NC(=O)C(C)(C)NC(=O)OCC1c2ccccc2-c2ccccc21)C(C)C
Reaction #161928
#55
収率 19.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(CC2CCCC=C2c2nc(-c3ccccc3)c(-c3ccccc3)o2)c1
Reaction #180473
DOI: 10.1039/C8SC04228D
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