部分構造検索

Nc1cccc2cccc(N)c12

COc1cccc([C@]23CCNC[C@@H]2CCC(=O)C3)c1.Cl
Reaction #2952
title compound
収率 70.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Br)c1ccc2ccccc2c1
Reaction #47124
(R)-1-Bromo-1-(2-naphthyl)ethane
DOI: 10.6084/m9.figshare.5104873.v1
COC1=C2C[C@@H](C)C[C@H](OC)[C@H](OC)[C@@H](C)/C=C(\C)[C@H](OC(N)=O)[C@@H](OC)/C=C\C=C(/C)C(=O)NC(=CC1=O)C2=O
Reaction #52148
11-O-methyl-geldanamycin
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Nc2cccc3c(N=Nc4c([N+](=O)[O-])ccc5ccccc45)ccc(c23)N1
Reaction #56102
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Nc2cccc3c(N=Nc4ccc([N+](=O)[O-])c5cc6ccccc6cc45)ccc(c23)N1
Reaction #56103
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.FC(F)(F)c1cccc(C2=Nc3cccc4cccc(c34)N2)c1
Reaction #56162
2-(m-trifluoromethylphenyl)-1H-perimidine hydrochloride
収率 95.4%DOI: 10.6084/m9.figshare.5104873.v1
F.FC(F)(F)Oc1ccc(C2=Nc3cccc4cccc(c34)N2)cc1
Reaction #56163
2-(p-TRIFLUOROMETHOXYPHENYL)-1H-PERIMIDINE HYDROFLUORIDE
DOI: 10.6084/m9.figshare.5104873.v1
Cl.FC(F)(F)C(F)(F)Oc1ccc(C2=Nc3cccc4cccc(c34)N2)cc1
Reaction #56164
product
収率 82.7%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ncns1)c1cc(F)c(Oc2ccc(Cl)cc2-c2ccnn2C2CNC2)cc1F
Reaction #74528
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(c1cscn1)S(=O)(=O)c1ccc(Oc2ccc(Cl)cc2-c2ccnn2C2CNC2)c(C#N)c1
Reaction #74630
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1OC)CC(c1ccccc1)C1=C2CNC1.Cl
Reaction #82427
6,7-dimethoxy-4-phenyl-2,3,4,5-tetrahydro-1H-benz[e]isoindole hydrochloride
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](NC(=O)OC(C)(C)C)C(=O)OCc1ccccc1
Reaction #89572
(S)-2-tert-butoxycarbonylamino-3-methoxy-propionic acid benzyl ester
収率 69.6%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)OC(C)(C)C)OC)N(C)C(=O)OCc1ccccc1
Reaction #161899
tert-butyl (3R,4S,5S)-4-{[(benzyloxy)carbonyl](methyl)amino}-3-methoxy-5-methylheptanoate
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1[C@@H](Cc2ccccc2)COC[C@H](N(C(=O)OC(C)(C)C)C(=O)OC(C)(C)C)C(=O)O[C@H]1C
Reaction #162923
tert-butyl N-[(3S,7S,8R,9S)-7-benzyl-8-methoxy-9-methyl-2-oxo-1,5-dioxonan-3-yl]-N-tert-butoxycarbonylcarbamate
収率 85.5%DOI: 10.6084/m9.figshare.5104873.v1
COCCCO[C@@H]1[C@@H](Cc2ccccc2)COC[C@H](NC(=O)OC(C)(C)C)C(=O)O[C@H]1C
Reaction #162931
tert-butyl ((3S,7S,8R,9S)-7-benzyl-8-(3-methoxypropoxy)-9-methyl-2-oxo-1,5-dioxonan-3-yl)carbamate
収率 72.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(C)CCO[C@@H]1[C@@H](Cc2ccccc2)COC[C@H](NC(=O)OC(C)(C)C)C(=O)O[C@H]1C
Reaction #162935
tert-butyl ((3S,7S,8R,9S)-7-benzyl-8-(3-methoxybutoxy)-9-methyl-2-oxo-1,5-dioxonan-3-yl)carbamate
収率 84.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1-c1cc(N2CCNCC2)ncc1N(C)C(=O)C(C)(C)c1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #185332
DOI: 10.1039/C8SC04228D
CCOC(C)OC1CCC(C)(OC)C(OC(C)=O)C=CC(C)C(C(C)=CC=CC(C)(CC2OC2C(C)C(CC)OC(C)OCC)OC(C)OCC)OC(=O)C1
Reaction #185552
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N(c1cscn1)S(=O)(=O)c1ccc(Oc2ccc(Cl)cc2-c2ccnn2C2CNC2)c(C#N)c1
Reaction #201623
DOI: 10.1039/C8SC04228D
OCC1(CO)Nc2cccc3cccc(c23)N1
Reaction #211767
DOI: 10.1039/C8SC04228D
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