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227011

[Li][c]1cccs1
Reaction #1465
lithiothiophene
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(/C(=C/c2ccc3c(c2)C(c2ccc(C)cc2)=CCC3(C)C)CC(OC)OC)cc1
Reaction #2702
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(-c2cccc3cc4c(cc23)C(c2ccc(C)nc2)=CCC4(C)C)cc1
Reaction #2709
Ethyl 4-[1-(6-methyl-pyrid-3-yl)-3,4-dihydro-4,4-dimethyl-anthracen-8-yl]-benzoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(/C(=C/c2ccc3c(c2)C(c2ccc(C)cc2)=CCC3(C)C)CC(OC)OC)cc1
Reaction #2721
product E
DOI: 10.6084/m9.figshare.5104873.v1
[Li][c]1cccs1
Reaction #52847
lithiothiophene
DOI: 10.6084/m9.figshare.5104873.v1
CC(=Cc1ccc(C(=O)O)cc1)c1ccc2c(c1)SCCC2(C)C
Reaction #65681
p-[2-(3,4-dihydro-4,4-dimethyl-2H-1-benzothiopyran-7-yl)propenyl]benzoic acid
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(/C(=C/CO)c2ccc(C(C)(C)C)cc2)ccc1Cl
Reaction #157708
title compound
Выход 101.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(/C(=C/CBr)c2ccc(C(C)(C)C)cc2)ccc1Cl
Reaction #157709
title compound
Выход 118.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(/C(=C/C(=O)O)c2ccc(C(C)(C)C)cc2)ccc1Cl
Reaction #157710
title compound
Выход 69.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(/C(=C/Br)c2ccc(C(C)(C)C)cc2)ccc1Cl
Reaction #157711
title compound
Выход 25.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(/C(=C/CC#N)c2ccc(C(C)(C)C)cc2)ccc1Cl
Reaction #157716
title compound
Выход 53.3%DOI: 10.6084/m9.figshare.5104873.v1
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)/[C](=C/[C@H]1CCC(=O)N1Cc1ccc(OC)cc1OC)c1ccc(C(C)(C)C)cc1
Reaction #157726
title compound
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(/C(=C/[C@H]2CCC(=O)N2)c2ccc(C(C)(C)C)cc2)ccc1Br
Reaction #157737
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COc2nc(/C(=C/[C@H]3CCC(=O)N3Cc3ccc(OC)cc3OC)c3ccc(C(C)(C)C)cc3)ccc2OC)cc1
Reaction #157821
(5R)-5-[(E)-2-(4-tert-butylphenyl)-2-{5-methoxy-6-[(4-methoxybenzyl)oxy]-pyridin-2-yl}ethenyl]-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(OC)c(=O)[nH]2)c(OC)c1
Reaction #157822
6-{(E)-1-(4-tert-butylphenyl)-2-[(2R)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidin-2-yl]ethenyl}-3-methoxypyridin-2(1H)-one
Выход 39.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(/C(=C/[C@H]2CCC(=O)N2)c2ccc(C(C)(C)C)cc2)[nH]c1=O
Reaction #157823
title compound
Выход 62.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COc2nc(/C(=C/[C@H]3CCC(=O)N3Cc3ccc(OC)cc3OC)c3ccc(C(C)(C)C)cc3)ccc2OC(F)F)cc1
Reaction #157824
(5R)-5-[(E)-2-(4-tert-butylphenyl)-2-{5-(difluoromethoxy)-6-[(4-methoxybenzyl)oxy]-pyridin-2-yl}ethenyl]-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(N)c(OC)n2)c(OC)c1
Reaction #157828
(5R)-5-[(E)-2-(5-amino-6-methoxypyridin-2-yl)-2-(4-tert-butylphenyl)ethenyl]-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(/C(=C/[C@H]2CCC(=O)N2)c2ccc(C(C)(C)C)cc2)ccc1N
Reaction #157829
(5R)-5-[(E)-2-(5-amino-6-methoxypyridin-2-yl)-2-(4-tert-butylphenyl)ethenyl]pyrrolidin-2-one
Выход 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(/C(=C\[C@H]2CCC(=O)N2)c2ccc(N)c(=O)[nH]2)cc1
Reaction #157830
title compound
Выход 44.0%DOI: 10.6084/m9.figshare.5104873.v1
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