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1025315

N#Cc1ccc(N2N=C3c4ccc(C(=O)OCC(=O)OCc5ccccc5)cc4CCC3C2C2CCCC2)cc1Cl
Reaction #175875
DOI: 10.1039/C8SC04228D
CC(C)OC(=O)c1ccc2c(c1)CCC1C2=NN(c2ccc(C#N)c(Cl)c2)C1C1CCCC1
Reaction #200804
DOI: 10.1039/C8SC04228D
N#Cc1ccc(N2N=C3c4ccc(C(=O)OCCc5ccccn5)cc4CCC3C2C2CCCC2)cc1Cl
Reaction #234605
DOI: 10.1039/C8SC04228D
N#Cc1ccc(N2N=C3c4ccc(C(=O)OCCC5CCCCC5)cc4CCC3C2C2CCCC2)cc1Cl
Reaction #267355
DOI: 10.1039/C8SC04228D
N#Cc1ccc(N2N=C3c4ccc(C(=O)OCCOCCOCCO)cc4CCC3C2C2CCCC2)cc1Cl
Reaction #271381
DOI: 10.1039/C8SC04228D
CCC(CC)OC(=O)c1ccc2c(c1)CCC1C2=NN(c2ccc(C#N)c(Cl)c2)C1C1CCCC1
Reaction #291729
DOI: 10.1039/C8SC04228D
COc1ccc(COC(=O)c2ccc3c(c2)CCC2C3=NN(c3ccc(C#N)c(Cl)c3)C2C2CCCC2)cc1
Reaction #390484
DOI: 10.1039/C8SC04228D
CCC(C)OC(=O)c1ccc2c(c1)CCC1C2=NN(c2ccc(C#N)c(Cl)c2)C1C1CCCC1
Reaction #395226
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc2c(c1)CCC1C2=NN(c2ccc(C#N)c(Cl)c2)C1C1CCCC1
Reaction #592899
(±)-(3SR,3aRS)-methyl 2-(3-chloro-4-cyanophenyl)-3-cyclopentyl-3,3a,4,5-tetrahydro-2H-benzo[g]indazole-7-carboxylate
Ausbeute 87.3%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N2N=C3c4ccc(C(=O)O)cc4CCC3C2C2CCCC2)cc1Cl
Reaction #592900
(±)-(3SR,3aRS)-2-(3-chloro-4-cyanophenyl)-3-cyclopentyl-3,3a,4,5-tetrahydro-2H-benzo[g]indazole-7-carboxylic acid
Ausbeute 105.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCc3cc(C(=O)O)ccc3C1=NN(c1ccc(C#N)c(Cl)c1)[C@H]2C1CCCC1
Reaction #592929
title compound
Ausbeute 30.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(=O)c1ccc2c(c1)CCC1C2=NN(c2ccc(C#N)c(Cl)c2)C1C1CCCC1
Reaction #592938
title compound
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N2N=C3c4ccc(C(=O)OCCC5CCCCC5)cc4CCC3C2C2CCCC2)cc1Cl
Reaction #592939
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N2N=C3c4ccc(C(=O)OCC5CCCCC5)cc4CCC3C2C2CCCC2)cc1Cl
Reaction #592940
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)OC(=O)c1ccc2c(c1)CCC1C2=NN(c2ccc(C#N)c(Cl)c2)C1C1CCCC1
Reaction #592941
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCOCCOCCOC(=O)c1ccc2c(c1)CCC1C2=NN(c2ccc(C#N)c(Cl)c2)C1C1CCCC1
Reaction #592942
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N2N=C3c4ccc(C(=O)OCCOCCOCCO)cc4CCC3C2C2CCCC2)cc1Cl
Reaction #592943
title compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N2N=C3c4ccc(C(=O)OCCN(CCO)CCO)cc4CCC3C2C2CCCC2)cc1Cl
Reaction #592944
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)OC(=O)c1ccc2c(c1)CCC1C2=NN(c2ccc(C#N)c(Cl)c2)C1C1CCCC1
Reaction #592945
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N2N=C3c4ccc(C(=O)OC5CCCCC5)cc4CCC3C2C2CCCC2)cc1Cl
Reaction #592946
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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