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CN(C)C1CCCCC1O

CC(c1cccc(OC(F)(F)F)c1)C1(O)CCCCC1N1CC[C@H](N)C1.Cl.Cl
Reaction #57102
2-[(3S)-3-aminopyrrolidin-1-yl]-1-[3-(trifluoromethoxy)phenyl]ethylcyclohexanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CN[C@H]1CCN(C2CCCCC2(O)C(C)c2cccc(C(F)(F)F)c2)C1.Cl.Cl
Reaction #57103
2-[(3S)-3-(methylamino)pyrrolidin-1-yl]-1-[3-(trifluoromethyl)phenyl]ethylcyclohexanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.N[C@@H]1CCN(CC(c2ccc3ccccc3c2)C2(O)CCCCC2)C1
Reaction #57119
1-[2-[(3R)-3-aminopyrrolidin-1-yl]-1-(2-naphthyl)ethyl]cyclohexanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(c1ccc(OCc2ccccc2)c(Cl)c1)C1(O)CCCCC1N1CCC(N)CC1.Cl.Cl
Reaction #57127
2-(4-aminopiperidin-1-yl)-1-[4-(benzyloxy)-3-chlorophenyl]ethylcyclohexanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.OC1(C(CN2CCNCC2)c2ccc(OCc3ccccc3C(F)(F)F)cc2)CCCCC1
Reaction #57128
1-[2-piperazin-1-yl-1-(4-{[2-(trifluoromethyl)benzyl]oxy}phenyl)ethyl]cyclohexanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1C[C@@H]2CC[C@@H]3[C@H](CC[C@]4(C)C(=O)[C@@H](N5CCCCC5)C[C@@H]34)[C@@]2(C)C[C@@H]1N1CCCCC1
Reaction #65119
(2β,3α,5α,16β)-3-acetyloxy-2,16-di-(1-piperidinyl)androstan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(=O)OC2CCC(c3ccncc3N)CC21
Reaction #160763
tert-butyl 5-(3-aminopyridin-4-yl)-2-oxohexahydrobenzo[d]oxazole-3(2H)-carboxylate
Выход 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(c2ccncc2N)CC2C1OC(=O)N2C(=O)OC(C)(C)C
Reaction #160771
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC1(OCC)CCN(Cc2ccccc2)[C@@H]2CCCC[C@@]21O
Reaction #160794
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O[C@]12CCCC[C@H]1N(Cc1ccccc1)CC[C@H]2Nc1ccccc1
Reaction #160795
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Reaction #162868
alcohol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCN(C2CCCCC2OCc2ccccc2)C1
Reaction #180053
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #187241
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #199343
DOI: 10.1039/C8SC04228D
CC(C)C(=O)OC1CC2CCC3C(CCC4(C)C(O)C(N5CCCCC5)CC34)C2(C)CC1N1CCCCC1
Reaction #227637
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #229157
DOI: 10.1039/C8SC04228D
CCC1(c2cccc(O)c2)CN(C)C2CCCCC2O1
Reaction #230437
DOI: 10.1039/C8SC04228D
O=C1NCC(c2ccccc2)C12CCN(C1CCCCC1(O)c1ccc(F)cc1)CC2
Reaction #241549
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #262825
DOI: 10.1039/C8SC04228D
COc1ccc(-c2sc3cc(OC)ccc3c2C(=O)c2ccc(OC3CCCCC3N3CCCCC3)cc2)cc1
Reaction #268845
DOI: 10.1039/C8SC04228D
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