Recherche de Sous-structure

1045150

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)c1cc(Br)c(NC(C)=O)c(I)c1O
Reaction #45816
Methyl 4-acetylamino-5-bromo-3-iodosalicylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Br)c(NC(C)=O)c(C#CC(C)(C)C)c1O
Reaction #45817
Methyl 4-acetylamino-5-bromo-3-(3,3-dimethyl-1-butynyl)salicylate
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
Rendement 33.8%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
Rendement 33.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(NN)cc1OC
Reaction #87527
desired product
Rendement 108113.0%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
Rendement 89.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-n2nc(-c3c(F)cccc3Cl)[nH]c2=O)cc1OC
Reaction #87529
desired product
Rendement 87.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3c(F)cccc3Cl)[nH]c2=O)ccc1C(=O)O
Reaction #87530
desired product
Rendement 0.1%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
Rendement 86.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-n2nc(-c3c(Cl)cccc3Cl)[nH]c2=O)cc1OC
Reaction #87540
desired product
Rendement 103.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-n2nc(-c3cc(CNC(=O)C(F)(F)F)ccc3Cl)[nH]c2=O)cc1OC
Reaction #87547
desired product
Rendement 29.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3cc(CNC(=O)C(F)(F)F)ccc3Cl)[nH]c2=O)ccc1C(=O)Nc1cccc(C(F)(F)F)c1
Reaction #87548
desired product
Rendement 67.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-n2nc(-c3cc(CN)ccc3Cl)[nH]c2=O)cc1OC.Cl
Reaction #87554
desired product
Rendement 205.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-n2nc(-c3cc(CNC(=O)C4CC4)ccc3Cl)[nH]c2=O)cc1OC
Reaction #87555
desired product
Rendement 67.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3c(Cl)cccc3I)[nH]c2=O)ccc1C(=O)Nc1cccc(C(F)(F)F)c1
Reaction #87565
desired product
Rendement 59.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3c(Cl)cccc3Cl)[nH]c2=O)ccc1C(=O)Nc1ccc(SC)cc1
Reaction #87576
desired product
Rendement 42.0%DOI: 10.6084/m9.figshare.5104873.v1
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