Recherche de Sous-structure

C=CC(=C)C

C#CC[C@@]1(O)CC[C@@H]2[C@@H]3CCC4=CC(=O)CCC4=C3[C@@H](c3ccc(C(C)=O)cc3)C[C@@]21C
Reaction #5434
title compound
Rendement 69.6%DOI: 10.6084/m9.figshare.5104873.v1
C=CC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #5641
title compound
Rendement 88.8%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C\C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #5642
title compound
Rendement 92.9%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C\C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #5644
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #42260
solid
Rendement 43.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #42261
solid
Rendement 13.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #42266
solid
Rendement 83.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #42267
solid
Rendement 39.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #45532
solid
Rendement 43.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #45533
solid
Rendement 13.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #45538
solid
Rendement 83.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #45539
solid
Rendement 39.0%DOI: 10.6084/m9.figshare.5104873.v1
N[C@H]1CC2=CNC=C3C=COCC1=C32
Reaction #53611
titled compound ( 31 )
Rendement 86.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #65627
title compound
Rendement 88.8%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C\C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #65628
title compound
Rendement 92.9%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C\C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #65630
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(C(=O)CCCN2CCC(C(O)(c3ccccc3)c3ccccc3)CC2)C=CC1CCO
Reaction #81618
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C=O)c1ccc(C(=O)CCCN2CCC(C(O)(c3ccccc3)c3ccccc3)CC2)cc1
Reaction #81619
4-[4-[4-(hydoxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl]-α,α-dimethylbenzeneacetaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)/C=C/CC(=O)O
Reaction #82447
trans-4-methyl-2,4-pentadienecarboxylic acid
Rendement 76.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(c2cccc(-c3ccccc3)c2)=C(c2ccc(Br)cc2)C(c2ccc(Br)cc2)=C1c1cccc(-c2ccccc2)c1
Reaction #85586
tetraarylcyclopentadienone
Rendement 53.1%DOI: 10.6084/m9.figshare.5104873.v1
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