Substructure Search

478915

COCc1nc2ccccc2n1Cc1ccc2c(c1)COc1cc(F)ccc1/C2=C(\C)C#N
Reaction #956686
title compound
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1
C/C(C#N)=C1/c2ccc(Cn3c(C(C)C)nc4ccccc43)cc2COc2cc(F)ccc21
Reaction #956687
title compound
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1
C/C(C#N)=C1/c2ccc(Cn3c(C4CC4)nc4ccccc43)cc2COc2cc(F)ccc21
Reaction #956688
title compound
Yield 96.3%DOI: 10.6084/m9.figshare.5104873.v1
C/C(C#N)=C1/c2ccc(Cn3c(C4CCC4)nc4ccccc43)cc2COc2cc(F)ccc21
Reaction #956689
title compound
Yield 90.3%DOI: 10.6084/m9.figshare.5104873.v1
C/C(C#N)=C1/c2ccc(Cn3c(C4CCCC4)nc4ccccc43)cc2COc2cc(F)ccc21
Reaction #956690
title compound
Yield 95.3%DOI: 10.6084/m9.figshare.5104873.v1
C/C(C#N)=C1/c2ccc(Cn3c(CC4CC4)nc4ccccc43)cc2COc2cc(F)ccc21
Reaction #956691
title compound
Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2ccccc2n1Cc1ccc2c(c1)COc1cc(F)ccc1/C2=C(\C)C#N
Reaction #956692
title compound
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1
C/C(C#N)=C1/c2ccc(Cn3c(C(F)(F)F)nc4ccccc43)cc2COc2cc(F)ccc21
Reaction #956693
title compound
Yield 88.9%DOI: 10.6084/m9.figshare.5104873.v1
C/C(C#N)=C1/c2ccc(Cn3c(C4CC(F)(F)C4)nc4ccccc43)cc2COc2cc(F)ccc21
Reaction #956696
title compound
Yield 96.9%DOI: 10.6084/m9.figshare.5104873.v1
C/C(C#N)=C1/c2ccc(Cn3c(C4(C)CC4)nc4ccccc43)cc2COc2cc(F)ccc21
Reaction #956697
title compound
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1
C/C(C#N)=C1/c2ccc(Cn3c(-c4ccco4)nc4ccccc43)cc2COc2cc(F)ccc21
Reaction #956698
title compound
Yield 94.4%DOI: 10.6084/m9.figshare.5104873.v1
C/C(C#N)=C1/c2ccc(Cn3c(-c4ccccn4)nc4ccccc43)cc2COc2cc(F)ccc21
Reaction #956699
title compound
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1
COCc1nc2c(OC)cccc2n1Cc1ccc2c(c1)COc1cc(F)ccc1/C2=C(\C)C#N
Reaction #956702
(E)-2-(3-fluoro-8-{[4-methoxy-2-(methoxymethyl)-1H-benzo[d]imidazol-1-yl]methyl}dibenzo[b,e]oxepin-11(6H)-ylidene)propanenitrile
Yield 53.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2c(OC)cccc2n1Cc1ccc2c(c1)COc1cc(F)ccc1/C2=C(\C)C#N
Reaction #956705
title compound
Yield 54.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2c(CO)cccc2n1Cc1ccc2c(c1)COc1cc(F)ccc1/C2=C(\C)C#N
Reaction #956709
title compound
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1
COCc1nc2c(CO)cccc2n1Cc1ccc2c(c1)COc1cc(F)ccc1/C2=C(\C)C#N
Reaction #956712
title compound
Yield 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COCc1nc2c(Cl)cccc2n1Cc1ccc2c(c1)COc1cc(F)ccc1/C2=C(\C)C#N
Reaction #956714
title compound
Yield 90.3%DOI: 10.6084/m9.figshare.5104873.v1
COCc1nc2c(C(C)(C)O)cccc2n1Cc1ccc2c(c1)COc1cc(F)ccc1/C2=C(\C)C#N
Reaction #956715
title compound
Yield 99.6%DOI: 10.6084/m9.figshare.5104873.v1
C/C(C#N)=C1/c2ccc(Cn3c(C4CC4)nc4c(Cl)cccc43)cc2COc2cc(F)ccc21
Reaction #956719
title compound
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cnccc2n1Cc1ccc2c(c1)COc1cc(F)ccc1/C2=C(\C)C#N
Reaction #956720
title compound
Yield 14.0%DOI: 10.6084/m9.figshare.5104873.v1
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