Recherche de Sous-structure

161410

NC1Cc2ccccc2NC1=O
Reaction #51399
3-(R,S)-amino-1,2,3,4-tetrahydroquinolin-2-one
Rendement 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2cc(Cl)cc(Cl)c2C(c2ccc(OC)c(OC)c2)C1C
Reaction #75678
Compound 46
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2cc(Cl)cc(Cl)c2C(c2cc(OC)c(OC)cc2OC)C1C
Reaction #75679
Compound 47
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Cc2cc(C(=O)NS(C)(=O)=O)ccc2NC1c1cccc(N2CCNCC2)c1
Reaction #173149
DOI: 10.1039/C8SC04228D
CC(=O)N1CCN(c2cccc(C3Nc4c(cc(Cl)cc4C(=O)O)CC3(C)C)c2)CC1
Reaction #176142
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(F)c2c1CC(C)(C)C(c1cccc(N3CCOCC3)c1)N2
Reaction #182153
DOI: 10.1039/C8SC04228D
CC1(C)Cc2c(cc(Cl)cc2C(=O)NS(C)(=O)=O)NC1c1cccc(N2CCOCC2)c1
Reaction #186408
DOI: 10.1039/C8SC04228D
CC1(C)Cc2cc(C(=O)O)ccc2NC1c1ccc(Cl)c(NC(=O)C2CCCCC2)c1
Reaction #186601
DOI: 10.1039/C8SC04228D
CC1(C)Cc2cc(C(=O)NS(=O)(=O)C3CC3)ccc2NC1c1cc(Cl)cc(N2CCOCC2)c1
Reaction #187389
DOI: 10.1039/C8SC04228D
CCOC(=O)c1ccc2c(c1)CC(C)(C)C(c1cccc(NC(C)(C)C(=O)N(C)C)c1)N2
Reaction #187476
DOI: 10.1039/C8SC04228D
CC1(C)Cc2cc(C(=O)NS(=O)(=O)C3CC3)ccc2NC1c1cncc(N2CCOCC2)c1
Reaction #187832
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](C)(C)OCCCc1ccc2c(c1)NC(=O)C1CCCC21
Reaction #192355
DOI: 10.1039/C8SC04228D
CC(=O)OCCc1ccc2c(c1)NC(=O)C1CCCC21
Reaction #195400
DOI: 10.1039/C8SC04228D
CCN1CCCC1CNC(=O)c1cccc(C2Nc3ccc(C(=O)OC)cc3CC2(C)C)c1
Reaction #196069
DOI: 10.1039/C8SC04228D
CC1(C)Cc2cc(Cl)cc(C(=O)NS(C)(=O)=O)c2NC1c1cccc(N2CCOCC2)c1
Reaction #199189
DOI: 10.1039/C8SC04228D
CC(C)N1CCN(c2cc(F)cc(C3Nc4ccc(C(=O)O)cc4CC3(C)C)c2)CC1
Reaction #203107
DOI: 10.1039/C8SC04228D
CN1CCN(c2cccc(C3Nc4ccc(C(=O)NS(C)(=O)=O)cc4CC3(C)C)c2)C(=O)C1=O
Reaction #204618
DOI: 10.1039/C8SC04228D
CC1(C)Cc2cc(C(=O)O)ccc2NC1c1ccc(NC(=O)c2ccccn2)cc1
Reaction #205057
DOI: 10.1039/C8SC04228D
CC1(C)Cc2cc(C(=O)NS(C)(=O)=O)ccc2NC1c1ccc(N2CCOCC2)cc1
Reaction #205160
DOI: 10.1039/C8SC04228D
CN1C(=O)C(C)(C)C(O)c2ccccc21
Reaction #207554
DOI: 10.1039/C8SC04228D
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