子结构搜索

361980

Cc1nc2c(OCC3CCCCC3)cccn2c1C(=O)N[C@H]1C[C@@H](CO)N(C)C1.Cl.Cl
Reaction #92762
8-(cyclohexylmethoxy)-N-[(3S,5S)-5-(hydroxymethyl)-1-methylpyrrolidin-3-yl]-2-methylimidazo[1,2-a]pyridine-3-carboxamide dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc(C(CC(=O)OC)(c2ccc(C=C)cc2)c2ccc(C=C)cc2)cc1
Reaction #359265
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CON=C(C=O)c1ccccc1COc1cc(C)ccc1C
Reaction #366641
2-(2,5-dimethylphenoxymethyl)-α-methoxyiminophenylacetaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
CON=C(C=O)c1ccccc1ON=C(C)c1cccc(C(F)(F)F)c1
Reaction #366665
2-[(α-methyl-3-trifluoromethylbenzylidene)aminooxy]-α-methoxyiminophenylacetaldehyde
收率 49.1%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1cnc2c(c1)CCC(c1ccc(Cl)c(Cl)c1)O2
Reaction #367379
2-(3,4-dichlorophenyl)-3,4-dihydro-6-(methylsulfonyl)-2H-pyrano[2,3-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2nc(C(C)C)c(CO)c(-c3ccc(F)cc3)n2n1
Reaction #432203
desired compound
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(CO)ccc1O[Si](C)(C)C(C)(C)C
Reaction #457003
3-tert-butyl-4-((tert-butyldimethylsilyl)oxy)benzyl alcohol
收率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(/C=C/c1ccc(C(F)(F)F)cc1)=C\CO
Reaction #467113
title compound
收率 70.1%DOI: 10.6084/m9.figshare.5104873.v1
OC/C=C/c1ccc(C(F)(F)F)cc1
Reaction #467122
title compound
收率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
OC/C=C/C#Cc1ccc(C(F)(F)F)cc1
Reaction #467137
title compound
收率 87.2%DOI: 10.6084/m9.figshare.5104873.v1
OC/C=C/c1ccc(C(F)(F)F)cc1
Reaction #468610
title compound
收率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
OC/C=C/C#Cc1ccc(C(F)(F)F)cc1
Reaction #468628
title compound
收率 87.2%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc(C(CC(=O)OC)(c2ccc(C=C)cc2)c2ccc(C=C)cc2)cc1
Reaction #481213
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CC2=C(CCCC2)C(C#N)C1=O
Reaction #503774
2-butyl-3-oxo-1,2,3,4,5,6,7,8-octahydroisoquinoline-4-carbonitrile
收率 70.1%DOI: 10.6084/m9.figshare.5104873.v1
O=CC1CCC(F)(F)CC1
Reaction #533181
title compound
收率 115.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CC2=C(CCCC2)C(C#N)C1=O
Reaction #576484
2-butyl-3-oxo-1,2,3,4,5,6,7,8-octahydroisoquinoline-4-carbonitrile
收率 70.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(Cc1nc(-c2ccccc2)cs1)c1ccc(CO)cc1
Reaction #595177
title compound
收率 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCN(Cc1ccc(CO)cc1)c1nc(-c2ccc(C(F)(F)F)cc2)cs1
Reaction #595181
title compound
收率 75.4%DOI: 10.6084/m9.figshare.5104873.v1
O=CC1CCC(F)(F)CC1
Reaction #719784
title compound
收率 57.0%DOI: 10.6084/m9.figshare.5104873.v1
O=CC1CCC(F)(F)CC1
Reaction #803074
title compound
收率 57.0%DOI: 10.6084/m9.figshare.5104873.v1
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