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N#CC1(c2ccc(N)cn2)CCC2(CC1)OCCO2

Reaction #1835693

titled compound

DOI: 10.6084/m9.figshare.5104873.v1

Cc1ccc(-n2ncc(C(=O)Nc3ccc(C4(C#N)CCC5(CC4)OCCO5)nc3)c2C)cc1

Reaction #1835814

titled compound

Ausbeute 2.6%DOI: 10.6084/m9.figshare.5104873.v1

Cc1ccc(-n2ncc(C(=O)Nc3ccc(C4(C#N)CCC(=O)CC4)nc3)c2C)cc1

Reaction #1835821

titled compound

Ausbeute 58.7%DOI: 10.6084/m9.figshare.5104873.v1

Cc1cc(NC(=O)c2cnn(-c3ncc(C(F)(F)F)cc3F)c2C)cnc1C1CCC(=O)CC1

Reaction #1835822

titled compound

Ausbeute 94.5%DOI: 10.6084/m9.figshare.5104873.v1

N#CC1(c2ccc(NC(=O)c3cncc(Br)c3)cn2)CCC2(CC1)OCCO2

Reaction #1835840

5-bromo-N-[6-(8-cyano-1,4-dioxaspiro[4.5]dec-8-yl)pyridin-3-yl]nicotinamide

Ausbeute 13.2%DOI: 10.6084/m9.figshare.5104873.v1

N#CC1(c2ccc(NC(=O)c3cncc(-c4ccc(F)cc4)c3)cn2)CCC2(CC1)OCCO2

Reaction #1835841

titled compound

Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)c1ccc(-n2cc(C(=O)Nc3ccc(C4(C#N)CCC(=O)CC4)nc3)cn2)cc1

Reaction #1835842

titled compound

Ausbeute 101.0%DOI: 10.6084/m9.figshare.5104873.v1