Teilstruktursuche

154997

CNCc1cn(C)c2c(C)cccc12
Reaction #46551
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC1=CCNC(=O)c2[nH]c3ccccc3c21
Reaction #58060
(1-oxo-1,2,3,10-tetrahydro-azepino[3,4-b]indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C=O)c2ccc(OC)cc2n1Cc1ccccn1
Reaction #68376
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C(=O)O)c2ccc(OC)cc2n1Cc1ccccn1
Reaction #68377
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C(=O)NCc2ccc(F)c(F)c2)c2ccc(OC)cc2n1Cc1ccccn1
Reaction #68378
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(C(=O)NCc3ccc(F)c(F)c3)c(C=O)n(Cc3ccccn3)c2c1
Reaction #68379
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1ccc2c(C(=O)NCc3ccc(F)c(F)c3)c(C(=O)NCCO)n(Cc3ccccn3)c2c1
Reaction #68382
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1ccc2c(C(=O)NCc3ccc(F)c(F)c3)c(C3=NCCO3)n(Cc3ccccn3)c2c1
Reaction #68383
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(C(=O)NCc3ccc(F)c(F)c3)c(C(=O)O)n(Cc3ccccn3)c2c1
Reaction #68447
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccc(F)c(F)c1)c1c(C(=O)O)n(Cc2ccccn2)c2cc(O)ccc12
Reaction #68448
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCCn1c(C(=O)OCC)c(-c2ccccc2)c2cc(OCc3ccccc3)ccc21
Reaction #95103
5-(2-Ethoxycarbonyl-5-benzyloxy-3-phenyl-1H-indole-1-yl)-valeric acid-ethylester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCCn2c(c(-c3ccccc3)c3cc(OCc4ccccc4)ccc32)C1=O
Reaction #95104
2-Benzyloxy-7,8,9,10-tetrahydro-10-oxo-11-phenyl-6H-9-azepino-[1,2-a]indole carboxylic acid ethylester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)c2ccccc2n1Cc1ccc(Cl)cc1
Reaction #170864
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)O)n(Cc2ccc(Cl)cc2)c2ccccc12
Reaction #170865
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)N2CCC(C(=O)NCc3ccccc3)CC2)n(Cc2ccc(Cl)cc2)c2ccccc12
Reaction #170866
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c2n(c3ccccc13)CCC2O
Reaction #181744
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(CN)c2cc(F)ccc2n1Cc1csc2ccc(F)cc12
Reaction #184308
DOI: 10.1039/C8SC04228D
COC(=O)c1c(C(=O)O)c2ccc(OC)cc2n1Cc1ccccn1
Reaction #207852
DOI: 10.1039/C8SC04228D
COC(=O)c1c(-c2ccccc2Cl)c2cc(C)cc(C)c2n1C
Reaction #216052
methyl 3-(2-chlorophenyl)-1,5,7-trimethylindole-2-carboxylate
Ausbeute 58.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2c(-c3ccccc3)c3cc(Cl)ccc3n2CCN1CCN1CCCC1
Reaction #223454
DOI: 10.1039/C8SC04228D
Seite 1Weiter