部分構造検索

CC(C)(C)C

COc1ccc(C2(C(=O)O)CC2)cc1CO
Reaction #46189
1-(3-hydroxymethyl-4-methoxy-phenyl)-cyclopropanecarboxylic acid
収率 132.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCNCCc1ccc(CC(C)(C)C(=O)O)cc1
Reaction #76091
3-[4-(2-heptylamino-ethyl)-phenyl]-2,2-dimethyl-propionic acid
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
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(C(C)OC(=S)SC)c(OC)n2)c(OC)c1
Reaction #157836
O-[1-(6-{(E)-1-(4-tert-butylphenyl)-2-[(2R)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidin-2-yl]ethenyl}-2-methoxypyridin-3-yl)ethyl] S-methyl carbonodithioate
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(/C(=C/[C@H]2CCC(=O)N2Cc2ccc(OC)cc2OC)c2ccc(C(C)(C)C)cc2)nc1OC
Reaction #157837
(5R)-5-[(E)-2-(4-tert-butylphenyl)-2-(5-ethyl-6-methoxypyridin-2-yl)ethenyl]-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
収率 71.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(CCCCOS(C)(=O)=O)c(OC)n2)c(OC)c1
Reaction #157846
4-(6-{(E)-1-(4-tert-butylphenyl)-2-[(2R)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidin-2-yl]ethenyl}-2-methoxypyridin-3-yl)butyl methanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(CCCCN(C)C)c(OC)n2)c(OC)c1
Reaction #157847
(5R)-5-[(E)-2-(4-tert-butylphenyl)-2-{5-[4-(dimethylamino)butyl]-6-methoxypyridin-2-yl}ethenyl]-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(C)(C)C(=O)CN=[N+]=[N-])ccc1F
Reaction #171044
1-azido-3-(4-fluoro-3-methoxyphenyl)-3-methylbutan-2-one
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(C)(C)C(=O)CN)ccc1F.Cl
Reaction #171045
1-amino-3-(4-fluoro-3-methoxyphenyl)-3-methylbutan-2-one hydrochloride
収率 55.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(C)(C)CCC(=O)O)cc1C
Reaction #173249
DOI: 10.1039/C8SC04228D
CC(C)(C)c1ccccc1OC1CN(C(=O)CCC(=O)O)C1
Reaction #179955
DOI: 10.1039/C8SC04228D
CCOC(=O)C(=O)CC(C)(C)c1cccc(C)c1OC
Reaction #183737
DOI: 10.1039/C8SC04228D
COc1ccc(Br)cc1C(C)(C)CC(=O)C(=O)O
Reaction #186313
DOI: 10.1039/C8SC04228D
CN(CCO)C(=O)CC1CCN(C(=O)C2NC(CC(C)(C)C)C(C#N)(c3ccc(Cl)cc3F)C2c2cccc(Cl)c2F)CC1
Reaction #192114
DOI: 10.1039/C8SC04228D
CCOC(=O)C(O)(CC1(c2cccc(F)c2OC)CC1)C(F)(F)F
Reaction #195661
DOI: 10.1039/C8SC04228D
CCOCCn1c(NC2CCN(CCC3(c4ccc(Cl)c(Cl)c4)CCCN(C(=O)c4cc(OC)c(OC)c(OC)c4)C3)CC2)nc2ccccc21
Reaction #196540
DOI: 10.1039/C8SC04228D
CC(=O)Nc1cccc(C2CCN(CCCNC(=O)C(C)(c3ccccc3)c3ccccc3)CC2)c1
Reaction #204436
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C)(CC)c1cccc(OC)c1
Reaction #204542
DOI: 10.1039/C8SC04228D
CC(C)C(NC(=O)Cn1c(-c2ccccc2)ccc(NC(=O)NCc2ccccc2)c1=O)(O[SiH](C)C)C(C(C)(C)C)C(F)(F)F
Reaction #211463
DOI: 10.1039/C8SC04228D
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