子结构搜索

CC(C)(C(=O)N)O

CC#CC1(OC)C(=O)Nc2ccc(-c3cccc(Cl)c3)cc21
Reaction #7088
title compound
收率 15.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccccc2C1(O)c1ccccc1
Reaction #44898
3-hydroxy-3-phenyl-1,3-dihydro-indol-2-one
收率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C2(c3ccccc3)C(=O)Nc3ccccc32)c(NS(=O)(=O)c2ccc(C(C)(C)C)cc2)cc1O
Reaction #44900
desired product
收率 89.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc[c]([Mg][Br])c1
Reaction #59622
3-methoxyphenylmagnesium bromide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1C(=O)C(C)(C)Oc2ccc([N+](=O)[O-])cc21
Reaction #65400
ethyl (3,4-dihydro-2,2-dimethyl-6-nitro-3-oxo-2H1,4 -benzoxazin-4-yl)acetate
收率 80.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Oc2ccc([N+](=O)[O-])cc2N(CC(=O)c2ccccc2)C1=O
Reaction #65401
3,4-dihydro-2,2-dimethyl-6-nitro-3-oxo-4-phenacyl-2H-1,4-benzoxazine
收率 66.6%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C1(O)CCN(Cc2ccccc2)CC1
Reaction #75591
1-benzyl-4-hydroxy-4-piperidine carboxamide
收率 68.8%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cccc1C1(O)C(=O)NC(=O)NC1=O
Reaction #94868
title product
收率 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCn1cccc1C1(O)C(=O)NC(=O)NC1=O
Reaction #94869
title product
收率 64.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)C(O)(c2nc3ccccc3s2)C(=O)N1
Reaction #94873
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccc(Cl)cc2)c2cc(OC(C)(C)C(N)=O)ccc2n1C
Reaction #95193
2-[3-(4-Chlorophenyl)-1,2-dimethyl-1H-indole-5-yloxy]-2-methyl-propanoic acid amide
DOI: 10.6084/m9.figshare.5104873.v1
CCCn1c(C)c(-c2ccncc2)c2cc(OC(C)(C)C(=O)N(CC)CC)ccc21
Reaction #95196
2-Methyl-2-[2-methyl-1-propyl-3-(4-pyridyl)-1H-indole-5-yloxy]-propanoic acid diethylamide
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)CC1(O)C(=O)Nc2ccc(I)cc21
Reaction #158214
2-(3-Hydroxy-5-iodo-2-oxo-2,3-dihydro-1H-indol-3-yl)-N,N-dimethyl-acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC1(Oc2cc(F)c(F)c(F)c2)CCCNC1=O
Reaction #158390
title compound
收率 57.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@](O)(COc1ccc(C#N)c(F)c1)C(=O)Nc1ccc(C#N)c(C(F)(F)F)c1
Reaction #170293
(S)-N-(4-cyano-3-(trifluoromethyl)phenyl)-3-(4-cyano-3-fluorophenoxy)-2-hydroxy-2-methylpropanamide
收率 23.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(O)(C(=O)NCCCN2CCC(c3cc(NC(=O)C(C)C)c(F)cc3F)CC2)c2ccc(C)cc2)cc1
Reaction #178308
DOI: 10.1039/C8SC04228D
N#CCCN1C(=O)C(O)(c2ccccc2)c2ccccc21
Reaction #178596
DOI: 10.1039/C8SC04228D
NC(=O)C1(O)CCN(Cc2ccccc2)CC1
Reaction #184880
DOI: 10.1039/C8SC04228D
COc1ccc(C2(O)C(=O)Nc3ccc(C)cc32)cc1
Reaction #189226
DOI: 10.1039/C8SC04228D
O=C1Nc2c(Cl)cccc2C1(O)c1ccccc1
Reaction #191778
DOI: 10.1039/C8SC04228D
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