子结构搜索

COC(=O)CCO

COCC1(C(=O)OC(C)(C)C)CCc2ncc(NC(=O)OCc3ccccc3)c(=O)n21
Reaction #11079
intermediate 23a
收率 36.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC1(C(=O)O)CCc2ncc(NC(=O)OCc3ccccc3)c(=O)n21
Reaction #11080
intermediate 23b
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](O)CSCc1ccccc1
Reaction #43569
(R)-3-Benzylsulfanyl-2-hydroxy-propionic acid methyl ester
收率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCO.OCC(O)CO
Reaction #46026
Ethanol Glycerol
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)COC(C)(C)C
Reaction #55059
rac.-methyl 3-tert. butoxy-2-methylpropionate
收率 43.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(=O)N[C@@H]1C(=O)N(CCOCc2ccccc2)c2ccccc2-c2ccccc21
Reaction #59281
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(=O)N[C@@H]1C(=O)N(CCOC)c2ccccc2-c2ccccc21
Reaction #59296
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](O)CO[Si](C)(C)C(C)(C)C
Reaction #59831
title compound
收率 59.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C(=O)C=CC(C)Oc1ccc(Oc2ccc(Cl)cc2Cl)cc1)C(=O)OC
Reaction #63426
faint yellow crystalline desired compound
收率 79.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1C(=O)Nc2ccc(Cl)cc2CC1c1ccc(OC)cc1
Reaction #63800
title compound
收率 91.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(OCc1ccccc1)OCc1ccccc1
Reaction #64664
ethyl 3,3-dibenzyloxypropionate
收率 99.6%DOI: 10.6084/m9.figshare.5104873.v1
O=CCC(OCc1ccccc1)OCc1ccccc1
Reaction #64665
3,3-dibenzyloxypropanal
收率 94.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(=O)N(c2ccc3[nH]cnc3c2)C1c1ccc(N2CCC(F)(F)CC2)cc1
Reaction #70031
1-(1H-Benzo[d]imidazol-5-yl)-5-(4-(4,4-difluoropiperidin-1-yl)phenyl)-pyrrolidine-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(=O)N(c2ccc3[nH]cnc3c2)C1c1ccc(OCCCC(F)F)cc1
Reaction #70032
1-(1H-Benzo[d]imidazol-5-yl)-5-(4-(4,4-difluorobutoxy)phenyl)-pyrrolidine-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1ccc(C2C(=O)CC(=O)N2c2ccc3[nH]cnc3c2)cc1
Reaction #70033
1-(1H-Benzo[d]imidazol-5-yl)-5-(4-butoxyphenyl)-pyrrolidine-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(=O)N(c2ccc3[nH]cnc3c2)C1c1ccc(N2CCSCC2)cc1
Reaction #70034
1-(1H-Benzo[d]imidazol-5-yl)-5-(4-thiomorpholinophenyl)-pyrrolidine-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CO)NC(=O)c1ccc([N+](=O)[O-])c(OC)c1
Reaction #71872
title compound
收率 69.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CO)NC(=O)c1ccc([N+](=O)[O-])c(C)c1
Reaction #71908
title compound
收率 88.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1COC(=O)N1
Reaction #83114
(S)-4-carbomethoxy-2-oxazolidinone
收率 88.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](O)[C@H](NC(=O)[C@H](C)NC(=O)CN2CCOCC2)C(=O)O)cc1
Reaction #87085
(2S,3R)-3-hydroxy-3-(4-methoxyphenyl)-2-((S)-2-(2-morpholinoacetamido)propanamido)propanoic acid
收率 79.4%DOI: 10.6084/m9.figshare.5104873.v1
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