Teilstruktursuche

168378

COc1ccc2[nH]c(-c3cc([N+](=O)[O-])c(N)cc3OC)nc2n1
Reaction #3968
2-(2-Methoxy-4-amino-5-nitro-phenyl)-5-methoxy-imidazo[4,5-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)C(c1ccccc1)C(O)(C1CCN(C(=O)OCc3ccccc3)CC1)N(C)C2=O
Reaction #46149
benzyl-4-(3-hydroxy-6-methoxy-2-methyl-1-oxo-4-phenyl-1,2,3,4-tetra-hydroisoquinolin-3-yl)piperidine-1-carboxylate
Ausbeute 49.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(=O)n(C)c(C3CCN(C(=O)OCc4ccccc4)CC3)c(-c3ccccc3)c2c1
Reaction #46150
benzyl-4-(6-methoxy-2-methyl-1-oxo-4-phenyl-1,2-dihydroisoquinolin-3-yl)piperidine-1-carboxylate
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc2c(c1[N+](=O)[O-])C(=O)NC(=O)C2(C)C
Reaction #75381
4,4-dimethyl-7-acetamino-8-nitro-2H,4H-isoquinoline-1,3-dione
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)NC(=O)c2c1ccc(NC(=O)c1ccccc1)c2[N+](=O)[O-]
Reaction #75382
4,4-dimethyl-7-benzoylamino-8-nitro-2H,4H-isoquinoline-1,3-dione
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)Nc2ccc3c(c2[N+](=O)[O-])C(=O)NC(=O)C3(C)C)c(OC)c1
Reaction #75383
4,4-Dimethyl-7-(2,4-dimethoxybenzoyl amino)-8-nitro-2H,4H-isoquinoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(SC)ccc1C(=O)Nc1ccc2c(c1[N+](=O)[O-])C(=O)NC(=O)C2(C)C
Reaction #75384
4,4-Dimethyl-7-(2-methoxy-4-methylmercapto-benzoylamino)-8-nitro-2H,4H-isoquinoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)Nc1ccc2c(c1[N+](=O)[O-])C(=O)NC(=O)C2(C)C
Reaction #75386
4,4-Dimethyl-7-propionylamino-8-nitro-2H,4H-isoquinoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)NC(=O)c2c1ccc(NC(=O)C1CC1)c2[N+](=O)[O-]
Reaction #75388
4,4-Dimethyl-7-(cyclopropylcarbonyl-amino)-8-nitro-2H,4H-isoquinoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)C(C)(C)CNC2=O
Reaction #79920
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)C(=O)c1c-2n(CCCCl)c(=O)c2ccccc12
Reaction #160025
solid
Ausbeute 17.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CNC(=O)c2cc(NC(=O)c3cccnc3F)ccc21
Reaction #174662
DOI: 10.1039/C8SC04228D
CC(=N)NC1CCCCC1N1C(=O)c2ccccc2C(C(=O)NOCc2ccccc2)C1c1ccc(Cl)cc1Cl
Reaction #174872
DOI: 10.1039/C8SC04228D
CS(=O)CCN1C(=O)c2ccccc2C(C)(C)C1=O
Reaction #182341
DOI: 10.1039/C8SC04228D
CC1(C)CNC(=O)c2cc([N+](=O)[O-])ccc21
Reaction #183598
DOI: 10.1039/C8SC04228D
CS(=O)(=O)NC1CCCCC1N1C(=O)c2ccccc2C(C(=O)O)C1c1ccc(Cl)cc1Cl
Reaction #191258
DOI: 10.1039/C8SC04228D
CCN1CC(C)(C)c2ccc(N)cc2C1=O
Reaction #202043
DOI: 10.1039/C8SC04228D
CS(=O)(=O)NC1CCCCC1N1C(=O)c2ccccc2C(C(=O)NCCc2cccc(OCC(=O)O)n2)C1c1ccc(Cl)cc1Cl
Reaction #203819
DOI: 10.1039/C8SC04228D
CC(=O)OCc1cccc(C(C)NC(=O)C2c3ccccc3C(=O)N(C3CCCCC3NS(C)(=O)=O)C2c2ccc(Cl)cc2Cl)n1
Reaction #211595
DOI: 10.1039/C8SC04228D
COc1ccc(C(=O)Nc2ccc3c(c2[N+](=O)[O-])C(=O)NC(=O)C3(C)C)c(OC)c1
Reaction #213502
DOI: 10.1039/C8SC04228D
Seite 1Weiter