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406685

CN(Cc1ccccc1Sc1ccc2c(ccn2C(=O)OC(C)(C)C)c1)C(=O)OC(C)(C)C
Reaction #44896
5-{2-[(tert-butoxycarbonyl-methyl-amino)-methyl]-phenylsulfanyl}-indole-1-carboxylic acid tert-butyl ester
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(Cc1ccccc1Sc1ccc2c(ccn2C(=O)OC(C)(C)C)c1)C(=O)OC(C)(C)C
Reaction #44920
5-{2-[(tert-butoxycarbonyl-methyl-amino)-methyl]-phenylsulfanyl}-indole-1-carboxylic acid tert-butyl ester
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Oc1c2c(cc3c1=Nc1ccc(C(=O)OCC)c(C(=O)OC(C)(C)C)c1-3)=c1cc(C(=O)OC(C)C(=O)OC(C)(C)C)ccc1=N2
Reaction #62012
1,1′-diBOC-2,10-dicarbethoxy-6-ethoxycarbonyloxy-indolo[2,3-b]carbazole
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1ccc2cc(Br)c(F)cc21
Reaction #77790
5-Bromo-6-fluoro-indole-1-carboxylic acid tert-butyl ester
Ausbeute 84.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1ccc2cc(C#CCCCO)c(F)cc21
Reaction #77791
6-Fluoro-5-(5-hydroxy-pent-1-ynyl)-indole-1-carboxylic acid tert-butyl ester
Ausbeute 455.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c2ccc(C3CC3)cc2c2cc(C3CC3)ccc21
Reaction #90443
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c2ccc(C3CC3)cc2c2cc(C3CC3)ccc21
Reaction #90484
crude product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccncc1N1CCN(c2ccc3c(ccn3C(=O)OC(C)(C)C)c2)C1=O
Reaction #167256
5-[3-(4-Methyl-pyridin-3-yl)-2-oxo-imidazolidin-1-yl]-indole-1-carboxylic acid tert-butyl ester
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1ccc2cc(Br)c(F)cc21
Reaction #208601
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)n1ccc2cc(C#CCCCO)ccc21
Reaction #283640
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)n1ccc2cc(-c3ccncc3)ccc21
Reaction #291835
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)c1ccc(-c2ccccc2)cc1Nc1ccc2c(ccn2C(=O)OC(C)(C)C)c1
Reaction #299863
DOI: 10.1039/C8SC04228D
CN(Cc1ccccc1Sc1ccc2c(ccn2C(=O)OC(C)(C)C)c1)C(=O)OC(C)(C)C
Reaction #317031
5-{2-[(tert-butoxycarbonyl-methyl-amino)-methyl]-phenylsulfanyl}-indole-1-carboxylic acid tert-butyl ester
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c2ccc(C3CC3)cc2c2cc(C3CC3)ccc21
Reaction #419281
crude product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cn(C(=O)OC(C)(C)C)c2cc(Cl)c(-c3ccc(O)cc3)cc12
Reaction #425630
title compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Br)cc2c(C3CCS(=O)(=O)CC3)c[nH]c12
Reaction #474433
5-Bromo-3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-1H-indole-7-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Br)cc2c(C3CCS(=O)(=O)C3)c[nH]c12
Reaction #474436
title compound
Ausbeute 30.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(-c2ccccc2)cc2c(C3CCCS(=O)(=O)CC3)c[nH]c12
Reaction #474445
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1cc(Br)cc2c(C3CCCS(=O)(=O)CC3)c[nH]c12
Reaction #474447
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(c2c[nH]c3c(C(=O)O)cc(Br)cc23)CCS1(=O)=O
Reaction #474463
title compound
Ausbeute 94.5%DOI: 10.6084/m9.figshare.5104873.v1
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