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5485

CC(C)OC(=O)Cn1c(=O)n(C)c(=O)n(-c2ccc(F)cc2Cl)c1=O
Reaction #1565
title product
収率 92.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(=O)Cn1c(=O)n(CC(=O)OC(C)C)c(=O)n(-c2cc(N=c3sc(=O)n4n3CCCC4)c(F)cc2Cl)c1=O
Reaction #1584
title product
収率 29.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)COc1ccc(CC(=O)OCc2ccccc2)cc1
Reaction #2321
tertiary butyl 4-(benzyloxycarbonylmethyl)phenoxyacetate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2c(NS(=O)(=O)c3ccc(C(C)(C)C)cc3)ncnc2OCCOc2ccc(OCC(=O)OC(C)(C)C)cc2)cc1
Reaction #2383
tert-butyl 4-{2-(6-(4-tert-butybenzenesulfonylamino)-5-(4-methylphenyl)pyrimidin-4-yloxy)ethoxy}phenoxyacetate
収率 92.7%DOI: 10.6084/m9.figshare.5104873.v1
COCCOCOc1c(C#N)ccc(C(Br)C(=O)OC(c2ccccc2)c2ccccc2)c1OCOCCOC
Reaction #2673
Diphenylmethyl [4-cyano-2,3-bis-[(2-methoxy-ethoxy]-methoxy]phenyl]-bromoacetate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Cn1c(=O)c(-c2c(Cl)cccc2Cl)cc2cnc(N)nc21
Reaction #3276
[2-amino-6-(2,6-dichlorophenyl)-7-oxo-7H-pyrido[2,3-d]pyrimidin-8-yl]-acetic acid tert-butyl ester
収率 30.1%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCC(=O)OC(C)(C)C
Reaction #7433
t-butyl-2-methacryloyloxyacetate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCC(=O)N(C(CC)C(=O)OC(C)(C)C)CC1
Reaction #7497
diester
収率 94.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CC(=O)OC(C)(C)C)CCOCC1
Reaction #9629
methyl 4-(2-tert-butoxy-2-oxoethyl)tetrahydro-2H-pyran-4-carboxylate
収率 56.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CC(=O)C[C@H](O)CO
Reaction #10224
(5S)-5,6-dihydroxy-3-oxohexanoic tert-butyl ester
収率 116.1%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)[C@@H](C(=O)Nc1ccccc1)C[C@@]2(C)CC(=O)OC(C)(C)C
Reaction #11097
intermediate 38a
収率 59.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(O)CN1CCCC1
Reaction #11342
desired acid
収率 97.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1COCC(=O)OC(C)(C)C
Reaction #11739
title compound
収率 65.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)COc1cc(Cl)ccc1OCC(=O)N1CCN(Cc2ccc(F)cc2)C[C@H]1CC(N)=O
Reaction #11803
title compound
収率 87.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C(Br)C(=O)c1cnc(NC(=O)C(C)(C)C)cn1
Reaction #40277
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)COc1ccc(Cl)cc1-c1ccc(C(=O)N2CCCC2)c(Cl)c1
Reaction #44367
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](OCc1ccccc1)[C@H]1COCC(=O)N1
Reaction #44648
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c2c(c(O)c(=O)n1CC(=O)OC(C)(C)C)C(=O)N(Cc1ccc(F)c(Cl)c1)CC2
Reaction #46281
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CNCCCCO
Reaction #46295
tert-Butyl[(4-hydroxybutyl)amino]acetate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](OC(=O)C(Br)c1ccccc1)c1ccccc1
Reaction #46637
title compound
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
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