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232081

CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1
Reaction #10855
8-[3-[N-[(E)-3-(6-acetamidopyridin-3-yl)acryloylglycyl]-N-methylamino]-2,6-dichlorobenzyloxy]-2methylquinoline
Ausbeute 53.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCOc2cc(/C=C/C(=O)O)cnc21
Reaction #46497
title compound
Ausbeute 94.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)/C=C/c1cnc2c(c1)OCCN2
Reaction #46498
title compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(Cc1cn(C)c2c(Cl)cccc12)C(=O)/C=C/c1ccc(NCC(=O)O)nc1
Reaction #46616
title compound
Ausbeute 100.4%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)CNc1ccc(/C=C/C(=O)N(C)Cc2cn(C)c3c(Cl)cccc23)cn1
Reaction #46617
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(Cc1cn(C)c2ccccc12)C(=O)/C=C/c1cnc2c(c1)CC(N)C(=O)N2
Reaction #46618
title compound
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #57369
solid
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1nc2c(c(-c3ccc(F)cc3)c1/C=C/[C@@H](O)C[C@@H](O)CC(=O)O)CCCN2S(C)(=O)=O
Reaction #57370
solid
Ausbeute 96.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2ccc(C3CCN(C(C)(C)C)CC3)cn2)c2ccccc21
Reaction #69990
4-(1′-(tert-butyl)-1′,2′,3′,4′,5′,6′-hexahydro-3,4′-bipyridinyl-6-yl)-3,4-dihydro-2H-quinoxaline-1-carboxylic acid tert-butyl ester
Ausbeute 37.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)/C=C/c1cnc2c(c1)CC1(CCN(C(=O)OC(C)(C)C)CC1)C(=O)N2
Reaction #170088
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCS(=O)(=O)C1CN(C(=O)/C=C/c2cnc3c(c2)CCC(=O)N3)C1
Reaction #170146
title compound
Ausbeute 19.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccsc1COC1CN(C(=O)/C=C/c2cnc3c(c2)CCC(=O)N3)C1
Reaction #170169
solid
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #170196
solid
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #170201
solid
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #170202
solid
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
C/C(=N/OCC(F)(F)F)C1CN(C(=O)/C=C/c2cnc3c(c2)CCC(=O)N3)C1
Reaction #170238
title product
Ausbeute 74.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1oc2ccccc2c1CN(C)C(=O)C=Cc1cnc2c(c1)CN(CCCN1CCOCC1)CC(=O)N2
Reaction #178269
DOI: 10.1039/C8SC04228D
CCOC(=O)C=Cc1ccc(N(C(=O)OC(C)(C)C)C2CCN(Cc3ccc(C(=O)c4ccccc4)cc3)C2)nc1
Reaction #180912
DOI: 10.1039/C8SC04228D
CCOc1c(CN(C)C(=O)C=Cc2cnc3c(c2)CNC(C)(C)C(=O)N3)cccc1OC(F)(F)F
Reaction #183533
DOI: 10.1039/C8SC04228D
O=C(C=Cc1ccc(NC2CCN(C(=O)c3ccc(Cl)cc3)C2)nc1)NOC1CCCCO1
Reaction #185787
DOI: 10.1039/C8SC04228D
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