Busqueda de Subestructura

CCC=O

O=CC1c2c[nH]nc2CCN1S(=O)(=O)c1ccc(Cl)cc1
Reaction #44010
79
Rendimiento 81.9%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccc(Cl)cc1)N1CCc2n[nH]cc2C1c1nc2ccccc2[nH]1
Reaction #44011
80
Rendimiento 13.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC(N)CC1
Reaction #44480
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nc(N3CCN(C(=O)C4CCCO4)CC3)nc(N)c2cc1OC.C[O-].Cl
Reaction #64276
1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-(tetrahydro-2-furoyl)piperazine monohydrochloride methanolate
Rendimiento 77.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nc(N3CCN(C(=O)C4CCCO4)CC3)nc(N)c2cc1OC.C[O-].Cl
Reaction #64277
1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-(tetrahydro-2-furoyl)piperazine monohydrochloride methanolate
Rendimiento 87.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CN2CCN(C(=O)[C@H](C)O)CC2)sc2c(N3CCOCC3)nc(Cl)nc12
Reaction #70176
(S)-1-(4-((2-chloro-7-methyl-4-morpholinothieno[3,2-d]pyrimidin-6-yl)methyl)piperazin-1-yl)-2-hydroxypropan-1-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CN2CCN(C(=O)[C@H](C)O)CC2)sc2c(N3CCOCC3)nc(-c3cnc(N)nc3)nc12
Reaction #70177
(S)-1-(4-((2-(2-aminopyrimidin-5-yl)-7-methyl-4-morpholinothieno[3,2-d]pyrimidin-6-yl)methyl)piperazin-1-yl)-2-hydroxypropan-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)CCn2nc(-c3ccc(F)cc3)c(-c3ccncc3)c21
Reaction #83225
2-(4-fluorophenyl)-4-methyl-5-oxo-3-(pyridin-4-yl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine
Rendimiento 68.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CNc2c(-c3ccncc3)c(-c3ccc(F)cc3)nn2C1=O
Reaction #83239
6-ethoxycarbonyl-2-(4-fluorophenyl)-7-oxo-3-(pyridin-4-yl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine
Rendimiento 39.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(OS(=O)(=O)c2ccc([N+](=O)[O-])cc2)C(=O)O[C@@H]1C
Reaction #83733
(R)-2-(4-nitrobenzenesulphonyloxy)-3-methoxycarbonyl -2penten-4-olide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(NCc2ccccc2)C(=O)O[C@@H]1C
Reaction #83734
(R)-2-benzylamino-3-methoxycarbonyl-2-penten-4-olide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC(O)(c2cccc(Br)n2)CC1
Reaction #86227
tert-butyl 4-(6-bromopyridin-2-yl)-4-hydroxyazepane-1-carboxylate
Rendimiento 64.1%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(C(=O)O)CN(CC2CCCN2)C[C@@H]1CCCB(O)O
Reaction #89660
(3R,4S)-3-amino-4-(3-boronopropyl)-1-(pyrrolidin-2-ylmethyl)pyrrolidine-3-carboxylic acid
Rendimiento 96.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2cc(S(=O)(=O)NCc3ccccc3)c(Cl)cc2CC1Br
Reaction #94215
6-Benzylsulfamoyl-2-bromo-5-chloro-1-indanone
DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(C(=O)OC(C)(C)C)CCC1NC1CC1
Reaction #155950
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(C(C)OC(=S)SC)c(OC)n2)c(OC)c1
Reaction #157836
O-[1-(6-{(E)-1-(4-tert-butylphenyl)-2-[(2R)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidin-2-yl]ethenyl}-2-methoxypyridin-3-yl)ethyl] S-methyl carbonodithioate
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(/C(=C/[C@H]2CCC(=O)N2Cc2ccc(OC)cc2OC)c2ccc(C(C)(C)C)cc2)nc1OC
Reaction #157837
(5R)-5-[(E)-2-(4-tert-butylphenyl)-2-(5-ethyl-6-methoxypyridin-2-yl)ethenyl]-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
Rendimiento 71.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(CCCCOS(C)(=O)=O)c(OC)n2)c(OC)c1
Reaction #157846
4-(6-{(E)-1-(4-tert-butylphenyl)-2-[(2R)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidin-2-yl]ethenyl}-2-methoxypyridin-3-yl)butyl methanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(CCCCN(C)C)c(OC)n2)c(OC)c1
Reaction #157847
(5R)-5-[(E)-2-(4-tert-butylphenyl)-2-{5-[4-(dimethylamino)butyl]-6-methoxypyridin-2-yl}ethenyl]-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CCc1c(CCN2CC(C(=O)OC)C2)cccc1-c1cnc(-c2ccc(OC(C)C)c(C#N)c2)s1
Reaction #172993
DOI: 10.1039/C8SC04228D
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