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15518

Brc1ccc2c(c1)CCC2Nc1nc2ccccc2[nH]1
Reaction #44827
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc2c1CCC2NC(=O)CC(NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1
Reaction #60335
N-(4-Cyano-indan-1-yl)-3-(naphthalen-2-yl-sulfonylamino)-3-phenyl-propionamide
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)Cc1cccc2c1CCC2NC(=O)CC(NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1
Reaction #60336
N-(4-Dimethylaminomethyl-indan-1-yl)-3-(naphthalen-2-yl-sulfonylamino)-3-phenyl-propionamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC(NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)NC1CCc2c(CN3CCCCC3)cccc21
Reaction #60337
3-(Naphthalen-2-yl-sulfonylamino)-3-phenyl-N-(4-piperidin-1-ylmethyl-indan-1-yl)-propionamide
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc2c(c1)CCC2NC(=O)CC(NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1
Reaction #60338
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)Cc1ccc2c(c1)CCC2NC(=O)CC(NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1
Reaction #60339
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC(NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)NC1CCc2cc(CN3CCCCC3)ccc21
Reaction #60340
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCc1ccc2c(c1)CCC2NC(=O)CC(NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1
Reaction #60341
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2c(c1)[C@H]1NC(=O)O[C@H]1C2
Reaction #171160
(3aR,8aS)-5-amino-3,3a,8,8a-tetrahydroindeno[1,2-d]oxazol-2-one
Выход 69.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC2C(COS(N)(=O)=O)CC(Nc3cc(NC4CCc5ccccc54)ncn3)C2O1
Reaction #173128
DOI: 10.1039/C8SC04228D
CC(=O)OC1CC(n2ccc3c(NC4CCc5ccccc54)ncnc32)CC1COS(N)(=O)=O
Reaction #178812
DOI: 10.1039/C8SC04228D
COc1ccc(C2OCC3CC(n4ccc5c(NC6CCc7ccccc76)ncnc54)CC3O2)cc1
Reaction #180987
DOI: 10.1039/C8SC04228D
O=C(CC(NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)NC1CCc2c(CN3CCCCC3)cccc21
Reaction #183114
DOI: 10.1039/C8SC04228D
CC1CN(C2(C)CCNCC2)CCN1C1CCc2cc(Br)ccc21
Reaction #186437
DOI: 10.1039/C8SC04228D
O=C(C=Cc1ccc(-n2ccnc2)c(CO)c1)NC1CCc2ccccc21
Reaction #187340
DOI: 10.1039/C8SC04228D
CC1(C)OC2C(COS(N)(=O)=O)CC(n3cnc4c(NC5CCc6ccccc65)ncnc43)C2O1
Reaction #201033
DOI: 10.1039/C8SC04228D
CC1(C)OC2C(CO)OC(n3cnc4c(NC5CCc6ccccc65)nncc43)C2O1
Reaction #204289
DOI: 10.1039/C8SC04228D
CCOC1Cc2ccccc2C1Nc1nc(CC)c(-c2cnc(N(C)C)cc2C)nc1CC
Reaction #207999
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(NC(=O)Nc2ccc3nc(NC4CCc5ccccc54)ccc3c2)CC1
Reaction #226549
DOI: 10.1039/C8SC04228D
CC1=NC2(N=C1N)c1cc(-c3cncc(Cl)c3)ccc1CC21CCC1
Reaction #229006
DOI: 10.1039/C8SC04228D
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