子结构搜索

16671

Cc1cc(F)c(N)cc1O
Reaction #7577
2-fluoro-5-hydroxy-4-methylaniline
收率 47.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(CO)c2ccccc2n1
Reaction #53540
2-methyl-4-hydroxymethylquinoline
收率 27.0%DOI: 10.6084/m9.figshare.5104873.v1
[Na][Na]
Reaction #71316
disodium
DOI: 10.6084/m9.figshare.5104873.v1
[Na][Na]
Reaction #71317
disodium
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCn2c(C(=O)c3ccccc3)ccc21
Reaction #82178
5-benzoyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCn2c(C(=O)c3ccccc3)ccc21
Reaction #82181
ketorolac methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #83160
ammonium jarosite
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(CO)c2ccccc2n1
Reaction #89711
4-hydroxymethyl-2-methyl quinoline
收率 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)S(=O)(=O)[C@H]1NC(=O)[C@@H]1CO
Reaction #93717
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1c2c(nc3ccc(O)cc13)-c1cc3c(c(=O)n1C2)COC(=O)[C@]3(O)CC
Reaction #216707
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(O)CC(C)(C)N1OC1CCCCC1
Reaction #220812
title compound
收率 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)CC(C)(C)N1OC1CCCCC1
Reaction #220813
title compound
收率 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(O)CC(C)(C)N1OC1CCCCC1
Reaction #220840
title compound
收率 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(S(C)=O)ccc1-c1nc2ncc(O)cc2[nH]1
Reaction #310540
2-(2-Methoxy-4-methylsulfinyl-phenyl)-6-hydroxy-1H-imidazo[4,5-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(C)(C)[C@H](O)C1OC1[C@@H]1[C@@H](C/C=C\CCCC(=O)OC)[C@H](Cl)C[C@H]1O
Reaction #317125
Methyl (5Z)-(9R,11R,13RS,14RS,15S)-9-chloro-11,15-dihydroxy-16,16-dimethyl-13,14-epoxy-5-prostenoate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(-c2ccc(O)cc2F)c(=O)n1C(F)F
Reaction #344529
1-(2-fluoro-4-hydroxyphenyl)-4-difluoromethyl-4,5-dihydro-3-methyl-1,2,4-triazol-5(1H)-one
收率 60.7%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)CC[C@H](N)C(=O)O
Reaction #355771
L-Glutamine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)c(N)cc1O
Reaction #366704
2-fluoro-5-hydroxy-4-methylaniline
收率 47.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2c(c1)CCC(CN1CCC(O)(c3ccccc3)CC1)C2=O
Reaction #415438
2-(4-phenyl-4-hydroxypiperidinomethyl)-6-amino-1-tetralone
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@@H]1O[C@@H]1c1ccc(Cl)cc1
Reaction #428975
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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