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16545

N#Cc1cc(-c2ccc3c(c2)C2(CCCC2)C(=O)N3)ccc1F
Reaction #7110
title compound
Выход 10.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Nc2ccc(F)c(C#N)c2)CC1
Reaction #71630
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(Br)ccc1Oc1ccccc1-c1ccccc1
Reaction #74565
desired compound
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccncc1N1CCN(c2ccc(F)c(C#N)c2)C1=O
Reaction #167313
product
Выход 65.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cncn1-c1ccc(Br)cc1C#N
Reaction #175925
DOI: 10.1039/C8SC04228D
N#Cc1cc(C=O)ccc1F
Reaction #207896
DOI: 10.1039/C8SC04228D
CCOc1cc(N(C)C)c(C#N)cc1Br
Reaction #224641
DOI: 10.1039/C8SC04228D
CN1CCN(c2ccc(Br)cc2C#N)CC1
Reaction #245962
DOI: 10.1039/C8SC04228D
COc1ccc(CNc2ncnc3c2CN(c2ccc(Br)cc2C#N)CC3)cn1
Reaction #300185
DOI: 10.1039/C8SC04228D
C[Si](C)(C)C#Cc1ccc(F)c(C#N)c1
Reaction #327936
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(C#CC2CC2)ccc1F
Reaction #327945
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(-c2cnn(Cc3ccccc3)c2)ccc1F
Reaction #327958
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1Nc2ccc(-c3ccc(F)c(C#N)c3)cc2C(C)(C)O1
Reaction #365047
2-Fluoro-5-(2,4,4-trimethyl-1,4-dihydro-2H-3,1-benzoxazin-6-yl)benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)COc1ccc(Br)cc1C#N
Reaction #378341
DOI: 10.1039/C8SC04228D
N#Cc1cc(-c2cccc3[nH]ccc23)ccc1F
Reaction #379820
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(Nc2ccc(Br)cc2C#N)CC1
Reaction #401953
DOI: 10.1039/C8SC04228D
C[C@H](Oc1ccc(-c2ccc(F)c(C#N)c2)cc1)[C@H](O)CCc1cccnc1
Reaction #467181
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(Br)ccc1NCCN1CCOCC1
Reaction #467187
sub-titled compound
Выход 49.7%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1cc(Br)ccc1F
Reaction #467229
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(B(O)O)ccc1F
Reaction #467230
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
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