Recherche de Sous-structure

12443

Nc1ccc(-c2cc3[nH]c4ccc(O)cc4c3c3c2C(=O)NC3=O)cc1
Reaction #11115
4-(4-Aminophenyl)-9-hydroxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
Rendement 57.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(NC(=O)Nc2ccc(B3OC(C)(C)C(C)(C)O3)cc2)c1
Reaction #45404
desired product
Rendement 99.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cnc(N)c3c(-c4ccc(NC(=O)c5cc6ccccc6n5C)c(OC)c4)csc23)cn1
Reaction #45430
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(C(=O)Nc2ccc(B3OC(C)(C)C(C)(C)O3)cc2)cc2ccccc21
Reaction #45439
desired product
Rendement 70.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)Nc2ccc(B3OC(C)(C)C(C)(C)O3)cc2)oc2ccccc12
Reaction #57589
3-methyl-benzofuran-2-carboxylic acid [4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-amide
Rendement 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(NC(=O)c3cc4ccccc4o3)cc2)OC1(C)C
Reaction #57590
benzofuran-2-carboxylic acid [4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-amide
Rendement 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C2C=C(c3ccc(N4CCN(S(C)(=O)=O)CC4)cc3)CC1CC2
Reaction #68973
3-[4-(4-methanesulfonylpiperazin-1-yl)phenyl]-8-azabicyclo[3.2.1]oct-2-ene-8-carboxylic acid tert-butyl ester
Rendement 37.8%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)c1ccc(B2OC(C)(C)C(C)(C)O2)cc1
Reaction #85803
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)c1ccc(B2OC(C)(C)C(C)(C)O2)cc1
Reaction #85809
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(c1ccc(B2OC(C)(C)C(C)(C)O2)cc1)S(C)(=O)=O
Reaction #85845
N-methyl-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN(C)c1ccc(-c2cc3nccnc3c(NCC3CN(C(=O)OC(C)(C)C)CCC3(F)F)n2)cc1
Reaction #85928
title compound
Rendement 155.6%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(-c2ncn(-c3ccc(C(F)(F)F)cc3)n2)cc1
Reaction #90312
title compound
Rendement 74.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](OC(C)(C)C)c1c(C)nc2sc3c(c2c1-c1ccc(N)cc1)CCCC3
Reaction #92245
title compound
Rendement 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1nn(-c2ccccc2)c2cc(-c3ccc(-n4ccnc4)cc3)ccc12
Reaction #155894
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)S(=O)(=O)Nc1ccc(B2OC(C)(C)C(C)(C)O2)cc1
Reaction #157764
title compound
Rendement 57.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccc(NC(=O)Nc3cc(C(F)(F)F)ccc3F)cc2)c2c(N)ncnn2c1CN1CCCOCC1
Reaction #160888
desired product
Rendement 15.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2c(C)c(CN3CCOCC3)n3ncnc(N)c23)ccc1NC(=O)Nc1cc(C(F)(F)F)ccn1
Reaction #160890
desired product
Rendement 36.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2c(C)c(CN3CCOCC3)n3ncnc(N)c23)ccc1NC(=O)Nc1cc(C(F)(F)F)ccc1F
Reaction #160891
desired product
Rendement 16.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccc(NC(=O)Nc3cc(C(F)(F)F)ccn3)cc2)c2c(N)ncnn2c1CN1CCOCC1
Reaction #160892
desired product
Rendement 44.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2cc(F)c(NC(=O)Nc3cc(C(F)(F)F)ccc3F)cc2F)c2c(N)ncnn2c1CN1CCOCC1
Reaction #160893
desired product
Rendement 14.0%DOI: 10.6084/m9.figshare.5104873.v1
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