子结构搜索

CC(C)CCN

O=C1Nc2ccc([N+](=O)[O-])cc2/C1=C(/Nc1ccc(CN2CCC(Cc3ccccc3)CC2)cc1)c1ccccc1
Reaction #53152
(Z)-3-{1-[4-(4-phenylmethyl-piperidinomethyl)-phenylamino]-1-phenyl-methylidene}-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1c(-c2ccc(F)cc2)nc2cc(C3CCN(C(=O)OCc4ccccc4)CC3)ccn12
Reaction #61629
benzyl 4-[3-acetyl-2-(4-fluorophenyl)imidazo-[1,2-a]pyridin-7-yl]piperidine-1-carboxylate
收率 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)/C=C/C(=O)c1c(-c2ccc(F)cc2)nc2cc(C3CCN(C(=O)OCc4ccccc4)CC3)ccn12
Reaction #61630
benzyl 4-{3-[(2E)-3-(dimethylamino)prop-2-enoyl]-2-(4-fluorophenyl)imidazo[1,2-a]pyridin-7-yl}piperidin-1-carboxylate
收率 143.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1(NCc2ccc3c(c2)OCCO3)CCN(C(=O)OC(C)(C)C)CC1
Reaction #67952
tert-butyl 4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)-4-methylpiperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[C@H]1CCN(C(=O)OC(C)(C)C)C1
Reaction #85899
(S)-tert-butyl 3-acetylpyrrolidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(O)[C@H]1CCN(C(=O)OC(C)(C)C)C1
Reaction #85900
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)CCN(C(=O)OC(C)(C)C)CC1
Reaction #87160
tert-butyl 4-hydroxy-4-methylpiperidine-1-carboxylate
收率 92.9%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1CN(C(=O)OC(C)(C)C)CC1(NC(=O)C(F)(F)F)C(=O)Nc1ccccc1[N+](=O)[O-]
Reaction #89666
tert-butyl 4-allyl-3-[(2-nitrophenyl)carbamoyl]-3-[(trifluoroacetyl)amino]-pyrrolidine-1-carboxylate
收率 51.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1CN(C(=O)OC(C)(C)C)CC1(NC(=O)C(F)(F)F)C(=O)Nc1ccccc1N
Reaction #89667
tert-butyl 4-allyl-3-[(2-aminophenyl)carbamoyl]-3-[(trifluoroacetyl)amino]pyrrolidine-1-carboxylate
收率 99.1%DOI: 10.6084/m9.figshare.5104873.v1
C1CC(COC2CC2)CCN1
Reaction #156301
4-[(cyclopropyloxy)methyl]piperidine
收率 62.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(COC2CC2)CC1
Reaction #156307
tert-butyl 4-[(cyclopropyloxy)methyl]piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#CC1(CO)CCNCC1
Reaction #157964
4-(hydroxymethyl)piperidine-4-carbonitrile hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@H]([C@@H](C)C(=O)NCC1(c2ccccc2)CC1)[C@@H]1CCCN1C(=O)OC(C)(C)C
Reaction #161930
#57
收率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C(=O)OC(C)(C)C)C1(C2CC(=O)N(C(C)c3ccccc3)C2)CC1
Reaction #176079
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCC(C#N)(CCCCl)CC1
Reaction #177904
DOI: 10.1039/C8SC04228D
CCC1(NCc2cn(C(=O)OC(C)(C)C)c3nccc(C(=O)OC)c23)CCN(C(=O)OC(C)(C)C)CC1
Reaction #178630
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(NC(=O)OCc2ccccc2)(C(F)(F)COS(C)(=O)=O)C1
Reaction #185560
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC2CC2C1C=O
Reaction #186016
DOI: 10.1039/C8SC04228D
CN(CCC1CCC(C(=O)O)CC1)C(=O)OC(C)(C)C
Reaction #192434
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2(CCNCCO2)CC1
Reaction #192905
DOI: 10.1039/C8SC04228D
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