子结构搜索

COC(=O)c1ccc(N)cc1OC

COCCOc1cc(N)c(Cl)cc1C(=O)OC
Reaction #5467
title compound
收率 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCOc1cc(N)c(Cl)cc1C(=O)O
Reaction #5468
fine pale tan needles
收率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)COc1cc(N)c(Cl)cc1C(=O)O
Reaction #5470
fine colorless needles
收率 68.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)c(NC(C)=O)cc1OC
Reaction #5974
methyl 2-methoxy-4-acetylamino-5-chlorobenzoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(O)c(C(=O)O)cc1Cl
Reaction #5975
4-acetylamino-5-chlorosalicylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)c(NC(C)=O)c2c1OC1CCCCC21
Reaction #5978
methyl 1-acetylamino-2-chloro-5a,6,7,8,9,9a-hexahydrodibenzofuran-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(Cl)cc(C(=O)O)c2c1C1CCCCC1O2
Reaction #5979
1-amino-2-chloro-5a,6,7,8,9,9a-hexahydrodibenzofuran-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)c(NC(C)=O)c2c3c(oc12)CCCC3
Reaction #5981
methyl 1-acetylamino-2-chloro-6,7,8,9-tetrahydrodibenzofuran-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(Cl)cc(C(=O)O)c2oc3ccccc3c12
Reaction #5983
1-AMINO-2-CHLORODIBENZOFURAN-4-CARBOXYLIC ACID
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc([N+](=O)[O-])cc1OC
Reaction #60563
2-methoxy-4-nitro-benzoic acid methyl ester
收率 47.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)c(NC(C)=O)c([N+](=O)[O-])c1OC
Reaction #67939
11
收率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)c(N)c([N+](=O)[O-])c1OC
Reaction #67940
12
收率 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(NC(=N)N)ccc1C(=O)O.Cl
Reaction #78223
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)c(NC(C)=O)c2c1OCC=C2
Reaction #80303
methyl 5-(acetylamino)-6-chloro-2H-1-benzopyran-8-carboxylate
收率 33.8%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)COc1cc(NC(C)=O)ccc1C(=O)OC
Reaction #80304
methyl 4-(acetylamino)-2-[(2-methyl-2-propenyl)oxy]benzoate
收率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)c(NC(C)=O)c2c1OCC=C2
Reaction #80947
methyl 5-(acetylamino)-6-chloro-2H-1-benzopyran-8-carboxylate
收率 33.8%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)COc1cc(NC(C)=O)ccc1C(=O)OC
Reaction #80948
methyl 4-(acetylamino)-2-[(2-methyl-2-propenyl)oxy]benzoate
收率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(N(NC(=O)OC(C)(C)C)C(=O)NC(=O)c2c(F)cccc2Cl)cc1OC
Reaction #87528
desired product
收率 89.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-n2nc(-c3c(F)cccc3Cl)[nH]c2=O)cc1OC
Reaction #87529
desired product
收率 87.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(N(NC(=O)OC(C)(C)C)C(=O)NC(=O)c2c(Cl)cccc2Cl)cc1OC
Reaction #87539
desired product
收率 86.6%DOI: 10.6084/m9.figshare.5104873.v1
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