Busqueda de Subestructura

716811

CC1(C)CC(=O)Nc2ccccc21
Reaction #40658
1a
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCNc2ccccc21
Reaction #40659
1b
Rendimiento 93.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CCCCCC1(Cc2ccncn2)C(=O)N(c2ccccc2)c2ccccc21
Reaction #64645
desired product
Rendimiento 68.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CCCCCC1(Cc2cnccn2)C(=O)N(c2ccccc2)c2ccccc21
Reaction #64647
desired product
Rendimiento 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCC1(Cc2cnccn2)C(=O)N(c2ccccc2)c2ccccc21
Reaction #64648
desired product
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)Nc2cc(-c3nc4ccccc4[nH]3)ccc21
Reaction #64676
title compound
Rendimiento 37.2%DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=O)CC(C)(C)c2ccc(C#N)cc21
Reaction #64677
4,4-dimethyl-1-ethyl-1,2,3,4-tetrahydro-2-oxo-7-quinolinecarbonitrile
Rendimiento 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)Nc2cc(Br)ccc21
Reaction #80723
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)Nc2cc(C#C[Si](C)(C)C)ccc21
Reaction #80724
title compound
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1C(=O)CC(C)(C)c2ccc(C#C[Si](C)(C)C)cc21
Reaction #80728
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cccc(OCCCN2CCC(c3noc4cc(F)ccc34)CC2)c1
Reaction #83885
3-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-aniline
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)Nc2ccccc21
Reaction #161223
4,4-dimethyl-3,4-dihydro-1H-quinolin-2-one
Rendimiento 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCNc2ccccc21
Reaction #161224
4,4-dimethyl-1,2,3,4-tetrahydro-quinoline
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1=N[C@@]2(c3cccc(NC(=O)c4ccc(F)cn4)c3)CN(c3ncc(F)cn3)C[C@H]2CS1)c1ccccc1
Reaction #164764
title compound
Rendimiento 41.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc(C(=O)Nc2cccc([C@]34CN(c5ncc(F)cn5)C[C@H]3CSC(NC(=O)c3ccccc3)=N4)c2)cn1
Reaction #164766
title compound
Rendimiento 92.4%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C(=O)Nc2cccc([C@]34CN(c5ncc(F)cn5)C[C@H]3CSC(NC(=O)c3ccccc3)=N4)c2)nc1
Reaction #164770
title compound
Rendimiento 92.9%DOI: 10.6084/m9.figshare.5104873.v1
NC1=NC2(c3cc(NC(=O)c4ccc(F)cn4)ccc3F)CN(c3ncc(F)cn3)CC2CS1
Reaction #164773
title compound
Rendimiento 186.9%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(c3cccc(NC(=O)c4ccc(F)cn4)c3)CN(c3ncc(F)cn3)C[C@H]2CS1
Reaction #164774
N-[3-[(4aR,7aS)-2-amino-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-7a-yl]phenyl]-5-fluoro-pyridine-2-carboxamide
Rendimiento 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc(C(=O)Nc2cccc([C@]34CN(c5ncc(F)cn5)C[C@H]3CSC(N)=N4)c2)cn1
Reaction #164775
N-[3-[(4aR,7aS)-2-amino-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-7a-yl]phenyl]-5-methoxy-pyrazine-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NC1=N[C@@]2(c3cc(NC(=O)c4ccc(F)cn4)ccc3F)CN(c3ncc(F)cn3)C[C@H]2CS1
Reaction #164776
title compound
Rendimiento 38.0%DOI: 10.6084/m9.figshare.5104873.v1
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