部分構造検索

C=COC(C)=O

CCCCOC(=O)CCCCCSC1=C(OC(=O)CCC)C[C@@H](O)[C@@H]1/C=C/[C@@H](O)C[C@H](C)CCCC
Reaction #3126
butyl (11R,12S,13E,15S,17R)-9-butyryloxy-11,15-dihydroxy-17,20-dimethyl-7-thiaprosta-8,13-dienoate
収率 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@@H](/C=C/[C@@H]1C(SCCCCCC(=O)OC)=C(OC(=O)c2ccccc2)C[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C
Reaction #3127
methyl(11R,12S,13E,15S)-9-benzoyloxy-11,15-bis(tert-butyldimethylsiloxy)-7-thiaprosta-8,13-dienoate
収率 55.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H](O)/C=C/[C@@H]1C(SCCCCCC(=O)OC)=C(OC(=O)c2ccccc2)C[C@H]1O
Reaction #3128
methyl(11R,13E,15S)-9-benzoyloxy-11,15-dihydroxy-7-thiaprosta-8,13-dienoate
収率 88.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCSC1=C(OC(=O)CCC)C[C@@H](O)[C@@H]1/C=C/[C@@H](O)CCCCC
Reaction #3129
(11R,12S,13E,15S)-9-butyryloxy-11,15-dihydroxy-7-thiaprosta-8,13-diene
収率 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC[C@@H](C)C[C@H](O)/C=C/[C@@H]1C(SCCCCCC(=O)OC)=C(OC(=O)c2ccccc2)C[C@H]1O
Reaction #3130
methyl(11R,12S,13E,15S,17R)-9-benzoyloxy-11,15-dihydroxy-17,20-dimethyl-7-thiaprosta-8,13-dienoate
収率 28.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H](O)/C=C/[C@@H]1C(SCCCCCC(=O)OC)=C(OC(=O)[C@H](Cc2ccccc2)NC(=O)OCc2ccccc2)C[C@H]1O
Reaction #3131
methyl(11R,12S,13E,15S)-9-(N-benzyloxycarbonylphenylalanyloxy)-11,15-dihydroxy-7-thiaprosta-8,13-dienoate
収率 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@@H](/C=C/[C@@H]1C(SCCCCCC(N)=O)=C(OC(=O)CCC)C[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C
Reaction #3133
(11R,12S,13E,15S)-9-butyryloxy-11,15-bis(tert-butyldimethylsiloxy)-7-thiaprosta-8,13-dienamide
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H](O)/C=C/[C@@H]1C(SCCCCCC(N)=O)=C(OC(=O)CCC)C[C@H]1O
Reaction #3134
(11R,12S,13E,15S)-9-butyryloxy-11,15-dihydroxy-7-thiaprosta-8,13-dienamide
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(C(F)(F)F)ccc1C(=O)OC1=CC(=O)C2CCC1C2
Reaction #52572
2-methyl-6-trifluoromethylnicotinic acid 4-oxobicyclo[3.2.1]oct-2-en-2-yl ester
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #54890
ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC(=Cc1ccncc1)c1ccccc1)c1ccccc1
Reaction #70833
title compound
収率 62.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1n[nH]c2nc(-c3ccccc3)c(-c3ccncc3)c(-c3ccccc3)c12
Reaction #70846
title compound
収率 16.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1=C(c2c(C)cc(C)cc2C)C(=O)CC(C2CCOC2)C1
Reaction #71598
3-oxo-5-(tetrahydrofuran-3-yl)-2-(2,4,6-trimethylphenyl)cyclohex-1-enyl acetate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(CC)C(=O)OC1=C(c2ccc(C)cc2C)C(=O)CC(C)(C)C1
Reaction #75069
3-(2-ethylhexanoyloxy)-5,5-dimethyl-2-(2',4'-dimethylphenyl)-2-cyclohexenone
収率 51.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #75257
ester
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(OC)cc2c1C(OC(C)=O)=C(C)C2O
Reaction #75914
ethyl-(1-hydroxy-2-methyl-6-methoxy-indenyl) acetate
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(=O)OC2=CC(=O)CCC2)c(Cl)c1C1=NOC2OCCC12
Reaction #76422
3-Oxocyclohex-1-enyl 2-chloro-4-methylsulfonyl-3-(3a,4,5,6a-tetra-hydrofuro[3,2-d]isoxazol-3-yl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)c1ccc(C(=O)OC2=CC(=O)CCC2)c(Cl)c1C1=NOC2OCCC12
Reaction #76423
3-Oxocyclohex-1-enyl 2-chloro-4-ethylsulfonyl-3-(3a,4,5,6a-tetrahydrofuro[3,2-d]isoxazol-3-yl)-benzoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)O)c1cccc(C(=O)c2ccc3ccccc3c2)c1
Reaction #77920
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C#Cc2ccc3c(c2)C(C)(C)CC=C3OC(C)=O)cc1
Reaction #81665
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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