部分構造検索

771927

c1ccc(-c2nccc3ccccc23)cc1
Reaction #7432
1-phenylisoquinoline
収率 96.9%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Clc1ccccc1CN1CCc2sccc2C1
Reaction #74954
5-(2-chloro-benzyl)-4,5,6,7-tetrahydro-thieno[3,2-c]pyridine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1Cl
Reaction #75005
N-chlorophthalimide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1Cl
Reaction #75006
N-chlorophthalimide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1Cl
Reaction #75007
N-chlorophthalimide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN(C(=O)N[C@@H](C)c2ccc(Cl)cc2)c2ccc(C3CCCCC3)cc2)cc1
Reaction #77823
4-[3-[1(S)-(4-Chlorophenyl)ethyl]1-(4-cyclohexylphenyl)ureidomethyl]benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccnc(CS(=O)c2nc3cc(OC(F)F)ccc3[nH]2)c1OC
Reaction #213541
DOI: 10.1039/C8SC04228D
CON1C(c2ccc(Br)cc2)=CC=NC1c1c(F)cccc1F
Reaction #237181
DOI: 10.1039/C8SC04228D
Fc1cccc(F)c1C1N=CC=C(c2ccc(Br)cc2)N1Cl
Reaction #241923
DOI: 10.1039/C8SC04228D
Nc1ncc(C(F)(F)F)cc1Cl
Reaction #256690
DOI: 10.1039/C8SC04228D
C=C(C)C(C(=O)OCc1ccc([N+](=O)[O-])cc1)N1C(=O)C(NC(=O)COc2ccccc2)C1S(=O)Cl
Reaction #279551
DOI: 10.1039/C8SC04228D
O=C1c2ccccc2C(=O)N1Cl
Reaction #281487
DOI: 10.1039/C8SC04228D
C=C(C)C(C(=O)OCc1ccc([N+](=O)[O-])cc1)N1C(=O)C(NC(=O)COc2ccccc2)C1S(=O)Cl
Reaction #348496
p-Nitrobenzyl 3-Methyl-2-(2-chlorosulfinyl-4-oxo-3-phenoxyacetamido-1-azetidinyl)-3-butenoate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1Cl
Reaction #371906
DOI: 10.1039/C8SC04228D
ClN1CCNCCNCCNCCNCC1(Cl)c1ccccc1.[Mn+2]
Reaction #450590
Manganese(II)dichloro(2-Phenyl-1,4,7,10,13-pentaazacyclopentadecane)
収率 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc(CC)c1-c1nc(C(C)OC)c(Cl)n1C=O
Reaction #544584
2-(2,6-diethylphenyl)-1-methoxyethyl-4-chloro-imidazole-3-carboxaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2c(N3CCNCC3)nccc2c1
Reaction #700845
title compound
収率 105.6%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CS(=O)[C@@H]2C(NC(=O)COc3ccccc3)C(=O)N2C1C(=O)OCc1ccc([N+](=O)[O-])cc1
Reaction #703781
title compound
収率 23.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1Cl
Reaction #757011
DOI: 10.1039/C8SC04228D
COc1cc(C2=NC(C)(C)C(c3ccncc3)C2)cc(OC)c1OC
Reaction #762097
DOI: 10.1039/C8SC04228D
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