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1372007

CCCCC(=O)NNC(=O)C1CCN(c2ccccn2)CC1
Reaction #7008
title compound
Ausbeute 30.6%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #7014
solid
DOI: 10.6084/m9.figshare.5104873.v1
CSc1nccc(C(=O)N2CC(N(C)C)CN2C(=O)Cc2ccc(F)cc2)n1
Reaction #7746
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CSc1nccc(-c2c(-c3ccc(F)cc3)c(=O)n3n2CC(N(C)C)C3)n1
Reaction #7747
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CN(C(=O)Cc2ccc(F)cc2)N(C(=O)OCc2ccccc2)C1)N1CCOCC1
Reaction #7759
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CNN(C(=O)Cc2ccc(F)cc2)C1)N1CCOCC1
Reaction #7760
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CN(C(=O)Cc2ccc(F)cc2)N(C(=O)c2ccnc(Oc3ccccc3)n2)C1)N1CCOCC1
Reaction #7761
desired product
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1Cn2c(-c3ccnc(Oc4ccccc4)n3)c(-c3ccc(F)cc3)c(=O)n2C1)N1CCOCC1
Reaction #7762
desired product
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCNN1C1CCNCC1
Reaction #48509
title compound
Ausbeute 108.5%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #48545
solid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(C(=O)N(NC(=O)NS(=O)(=O)c2ccc(Cl)cc2)C(C)(C)C)c1
Reaction #49952
1-t-butyl-1-(3-toluoyl)-4-(4-chlorobenzenesulfonyl)semicarbazide
DOI: 10.6084/m9.figshare.5104873.v1
CSc1nccc(C(=O)N2CC(N(C)C)CN2C(=O)Cc2ccc(F)cc2)n1
Reaction #50954
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CSc1nccc(-c2c(-c3ccc(F)cc3)c(=O)n3n2CC(N(C)C)C3)n1
Reaction #50955
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CN(C(=O)Cc2ccc(F)cc2)N(C(=O)OCc2ccccc2)C1)N1CCOCC1
Reaction #50967
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CNN(C(=O)Cc2ccc(F)cc2)C1)N1CCOCC1
Reaction #50968
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CN(C(=O)Cc2ccc(F)cc2)N(C(=O)c2ccnc(Oc3ccccc3)n2)C1)N1CCOCC1
Reaction #50969
desired product
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1Cn2c(-c3ccnc(Oc4ccccc4)n3)c(-c3ccc(F)cc3)c(=O)n2C1)N1CCOCC1
Reaction #50970
desired product
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CNc1nnc([C@@H]2C[C@@H](OS(C)(=O)=O)CN2C(=O)OCc2ccc([N+](=O)[O-])cc2)s1
Reaction #65537
(2S, 4R)-4-methanesulfonyloxy-2-{5-(methylamino)-1,3,4-thiadiazol-2-yl }-1-(4-nitrobenzyloxycarbonyl)pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CN1CCOCC1)NNC(=O)c1cc(Br)cc2c1cnn2C1CCCCO1
Reaction #67100
title compound
Ausbeute 70.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc(C#CC(C)(C)C)cc1N(NC(=O)C(F)(F)F)C(=O)C1CCC(C)CC1
Reaction #67586
5-(3,3-dimethyl-but-1-ynyl)-3-[N-(4-methyl-cyclohexanecarbonyl)-N′-(2,2,2-trifluoro-acetyl)-hydrazino]-thiophene-2-carboxylic acid methyl ester
Ausbeute 96.7%DOI: 10.6084/m9.figshare.5104873.v1
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