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757486

COc1nc(/C(=C/[C@H]2CCC(=O)N2)c2ccc(OC3CCOCC3)c(Cl)c2)ccc1C1CC1
Reaction #157813
(5R)-5-[(E)-2-[3-chloro-4-(tetrahydro-2H-pyran-4-yloxy)phenyl]-2-(5-cyclopropyl-6-methoxypyridin-2-yl)ethenyl]pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC[C@H](/C=C(\c2ccc(O)c(Cl)c2)c2ccc(C3CC3)c(=O)[nH]2)N1
Reaction #157815
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(/C(=C/[C@H]2CCC(=O)N2)c2ccc(Cl)c(Cl)c2)ccc1C1CC1
Reaction #157861
(5R)-5-[(E)-2-(5-cyclopropyl-6-methoxypyridin-2-yl)-2-(3,4-dichlorophenyl)ethenyl]pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
Reaction #157862
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@@H]1/C=C/c1cccc(Cl)c1
Reaction #168579
tert-butyl (R)-2-[(E)-2-(3-chlorophenyl)vinyl]pyrrolidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Clc1cccc(/C=C/[C@H]2CCCN2)c1
Reaction #168580
(R)-2-[(E)-2-(3-chlorophenyl)vinyl]pyrrolidine
Выход 111.2%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cccc(/C=C/[C@H]2CCCN2c2ncnc3[nH]cnc23)c1
Reaction #168581
6-[(R)-2-((E)-2-(3-chlorophenyl)vinyl)pyrrolidin-1-yl]-9H-purine
Выход 16.5%DOI: 10.6084/m9.figshare.5104873.v1
CN1C2C=C(c3ccc(Cl)c(Cl)c3)CC1CC2
Reaction #195573
DOI: 10.1039/C8SC04228D
COC1=C(c2cc(Cl)cc(Cl)c2)C(=O)N2CCCC12Cc1ccc(C#N)cc1
Reaction #245605
DOI: 10.1039/C8SC04228D
CN1C2C=C(c3ccc(Cl)c(Cl)c3)CC1CC2
Reaction #1074764
title compound
Выход 53.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(C2=CC3CCC(C2)N3)cc1Cl
Reaction #1074765
title compound
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1
Reaction #1074767
off-white solid
Выход 22.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)CC(c2ccccc2)C1C=Cc1cccc(Cl)c1
Reaction #1231978
DOI: 10.1039/C8SC04228D
CN1C2C=C(c3ccc(Cl)c(Cl)c3)CC1CC2
Reaction #1644499
DOI: 10.1039/C8SC04228D
CN1C2C=C(c3ccc(Cl)c(Cl)c3)CC1CC2
Reaction #1958047
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1C2CCC1C(CO)=C(c1ccc(Cl)c(Cl)c1)C2
Reaction #2244552
DOI: 10.1039/C8SC04228D
CCC1=C(c2cc(Cl)cc(Cl)c2)C(=O)N2C[C@@H](O)C[C@@]12Cc1ccc(Br)cc1
Reaction #2310953
(6S, 7aS)-7a-(4-Bromobenzyl)-2-(3,5-dichlorophenyl)-1-ethyl-6-hydroxy-5,6,7,7a-tetrahydro-3H-pyrrolizin-3-one
Выход 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(c2cc(Cl)cc(Cl)c2)C(=O)N2CCCC12Cc1ccc(C#N)cc1
Reaction #2310954
4-{[6-(3,5-Dichlorophenyl)-7-methyl-5-oxo-2,3-dihydro-1H-pyrrolizin-7a(5H)-yl]methyl}benzonitrile
Выход 14.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(c2cc(Cl)cc(Cl)c2)C(=O)N2CCCC12Cc1ccc(C#N)cc1
Reaction #2310955
4-[6-(3,5-Dichloro-phenyl)-7-methoxy-5-oxo-2,3-dihydro-1H,5H-pyrrolizin-7 a-ylmethyl]-benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(c2cc(Cl)cc(Cl)c2)C(=O)N2CCCC12Cc1ccc(C#N)cc1
Reaction #2400541
DOI: 10.1039/C8SC04228D
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