子结构搜索

Nc1ccc(CCO)cc1

O=C(O)Cc1ccc(-n2sc3ccccc3c2=O)cc1
Reaction #3366
title compound
收率 69.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1csc(NC(=O)[C@@H](NC(=O)[C@H](NC(=O)OC(C)(C)C)c2ccc(NC(=O)OC(C)(C)C)cc2)[C@@H](C)c2ccccc2)n1
Reaction #61117
2-{(2S,3S)-2-[(R)-2-tert-butoxycarbonylamino-2-(4-tert-butoxycarbonylamino-phenyl)-acetylamino]-3-phenyl-butyrylamino}-thiazole-4-carboxylic acid methyl ester
收率 82.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(N)c(O)c1
Reaction #77980
title compound
收率 76.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc([N+](=O)[O-])c(O)c1
Reaction #77981
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)Cc1ccc(N2C(=O)C=CC2=O)cc1
Reaction #78021
powder
收率 59.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)Cc1ccc(-n2sc3ccccc3c2=O)cc1
Reaction #81960
title compound
收率 69.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(C(=O)O)c1ccc(N2CCOCC2)cc1
Reaction #84764
2-methoxy-2-(4-morpholinophenyl)acetic acid
收率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(C(=O)N(C)OC)c1ccc(N2CCOCC2)cc1
Reaction #84765
N,2-dimethoxy-N-methyl-2-(4-morpholinophenyl) acetamide
收率 90.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(OC)c1ccc(NS(=O)(=O)CCCCl)cc1
Reaction #84802
methyl 2-(4-(3-chloropropylsulfonamido)phenyl)-2-methoxyacetate
收率 99.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(OC)c1ccc(N2CCCS2(=O)=O)cc1
Reaction #84803
methyl 2-(4-(1,1-dioxidoisothiazolidin-2-yl)phenyl)-2-methoxyacetate
收率 75.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2ccn(C(=O)C(OC)c3ccc(N4CCOCC4)cc3)n2)cc(OC)c1Br
Reaction #84855
1-(3-(4-bromo-3,5-dimethoxyphenyl)-1H-pyrazol-1-yl)-2-methoxy-2-(4-morpholinophenyl) ethanone
收率 22.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccn(C(=O)C(OC)c3ccc(N4CCOCC4)cc3)n2)cc1OC
Reaction #84856
1-(3-(3,4-dimethoxyphenyl)-1H-pyrazol-1-yl)-2-methoxy-2-(4-morpholinophenyl)ethanone
收率 489.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC1(C(=O)O)c1ccc([N+](=O)[O-])cc1
Reaction #94567
1-(p-nitrophenyl)-cyclopropane-1,2-dicarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(SC)c1ccc(N)c(Cl)c1
Reaction #173867
DOI: 10.1039/C8SC04228D
CCOC(=O)C1(c2ccc(N)c(OCC3CC3)c2)CCCC1
Reaction #174002
DOI: 10.1039/C8SC04228D
OCCc1ccc(-n2ccc3cccnc32)cc1
Reaction #174782
DOI: 10.1039/C8SC04228D
CC(C)(C)c1cc(NC(=O)c2ccc(-c3ccc([N+](=O)[O-])cc3)o2)cc(C(C)(C)C)c1O
Reaction #179683
DOI: 10.1039/C8SC04228D
Cl
Reaction #183246
DOI: 10.1039/C8SC04228D
COC(=O)C(CC1CCC1)c1cc(Br)c(N)c(OCC(F)(F)F)c1
Reaction #185591
DOI: 10.1039/C8SC04228D
COc1ccc(-n2nc(C(F)(F)F)c3c2C(=O)N(c2ccc(C4(C(=O)N(C)OC)CC4)cc2)CC3)cc1
Reaction #186001
DOI: 10.1039/C8SC04228D
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