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16190

O=C1Nc2ccccc2C12CCCCC2
Reaction #7093
subtitled compound
Ausbeute 69.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc(Br)cc2C12CCCCC2
Reaction #7094
subtitled compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1cccc1-c1ccc2c(c1)C1(CCCCC1)C(=O)N2
Reaction #7095
subtitled compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cccc1-c1ccc2c(c1)C1(CCCCC1)C(=O)N2
Reaction #7096
subtitled compound
Ausbeute 92.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(OCC)N1C(=O)C2(CCCCC2)c2cc(-c3cc(F)cc(C#N)c3)ccc21
Reaction #7099
title compound
Ausbeute 56.4%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(F)cc(-c2cc(Br)c3c(c2)C2(CCCCC2)C(=O)N3)c1
Reaction #7100
title compound
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(F)cc(-c2cc(N)c3c(c2)C2(CCCCC2)C(=O)N3)c1
Reaction #7101
title compound
Ausbeute 52.2%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(-c2ccc3c(c2)C2(CCCCC2)C(=O)N3)cc1F
Reaction #7103
title compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #7106
product
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccccc2C12CCCCC2
Reaction #9407
subtitled compound
Ausbeute 69.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc(Br)cc2C12CCCCC2
Reaction #9408
subtitled compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1cccc1-c1ccc2c(c1)C1(CCCCC1)C(=O)N2
Reaction #9412
2-(1′,2′-dihydro-2′-oxospiro[cyclohexane-1,3′-[3H]indol]-5′-yl)-1H-pyrrole-1-carboxylic acid, tert-butyl ester
Ausbeute 77.3%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(C#N)ccc1-c1ccc2c(c1)C1(CCCCC1)C(=S)N2
Reaction #9413
product
Ausbeute 90.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(C(CCO)c2cccc(F)c2)c2ccccc2C12CCCCC2
Reaction #243217
DOI: 10.1039/C8SC04228D
COC1CC(=O)NCC(c2cccc(Cl)c2)C12C(=O)Nc1cc(Cl)ccc12
Reaction #270993
DOI: 10.1039/C8SC04228D
CC1(O)CCC2(CC1)C(=O)Nc1cc(Br)ccc12
Reaction #277863
DOI: 10.1039/C8SC04228D
O=C1Nc2ccccc2C12CCCCC2
Reaction #364165
subtitled compound
Ausbeute 69.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc(Br)cc2C12CCCCC2
Reaction #364166
subtitled compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1cccc1-c1ccc2c(c1)C1(CCCCC1)C(=O)N2
Reaction #364170
2-(1′,2′-dihydro-2′-oxospiro[cyclohexane-1,3′-[3H]indol]-5′-yl)-1H-pyrrole-1-carboxylic acid, tert-butyl ester
Ausbeute 77.3%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(C#N)ccc1-c1ccc2c(c1)C1(CCCCC1)C(=S)N2
Reaction #364171
product
Ausbeute 90.5%DOI: 10.6084/m9.figshare.5104873.v1
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