Recherche de Sous-structure

O=C(O)[C@H](O)[C@@H](O)C(=O)O

COc1cccc([C@]2(O)CCCC[C@H]2CN(C)C)c1
Reaction #1393
(1S,2S)-2-dimethylaminomethyl-1-(3-methoxy-phenyl)-cyclohexanol
Rendement 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)Cc1ccc([C@H]2CC[C@H](OC(=O)Cc3ccc(Cl)cc3)CC2)cc1.O=C([O-])C(O)C(O)C(=O)[O-]
Reaction #1759
trans-O-(4-Chlorophenylacetyl)-4-(4-dimethylaminomethylphenyl)-cyclohexanol tartrate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H]1[C@@H](CC(=O)[O-])CC[C@H]1O
Reaction #2467
(1R,2S,3R)-3-hydroxy-2-pentyl-1-cyclopentaneacetate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc([C@]2(O)CCCC[C@H]2CN(C)C)c1
Reaction #2490
(1S, 2S)-2-dimethylaminomethyl-1-(3-methoxy-phenyl)-cyclohexanol
Rendement 99.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)C(=O)c2ccc(NC(C)=O)cc2)c1.O=C(O)C(O)C(O)C(=O)O
Reaction #2621
title compound
Rendement 75.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C1(CCCN(C)CCc2ccccc2)C=CC=CC1CC=O
Reaction #4085
2-[3-[(Phenylethyl)methylamino]-propyl]-2-isopropylphenylacetaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)c2cc(OCc3ccc(C=O)cc3)ccc21
Reaction #6607
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1cccnc1C=O
Reaction #7241
3-n-propoxypyridine-2-carboxaldehyde
Rendement 113.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@H](O)[C@@H](O)C(=O)O.OC1CN(CCCOCCc2ccc3sccc3c2)C1
Reaction #7549
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol L-tartrate
Rendement 91.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(-c2nn3c(c2-c2ccnc4cc(CCC(=O)N(C)C)ccc24)CCC3)n1
Reaction #8366
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(COc2ccc3c(-c4c(-c5ccccn5)nn5c4CCC5)ccnc3c2)C1
Reaction #8372
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc2c(c1O)Cc1cccc3c1[C@@H]2CNC3
Reaction #8808
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCc1nc(CO)co1
Reaction #9002
(4-hydroxymethyl-oxazol-2-ylmethyl)-carbamic acid tert-butyl ester
Rendement 28.4%DOI: 10.6084/m9.figshare.5104873.v1
OCc1ccc(-c2nc3ccccc3s2)cc1
Reaction #9069
title compound
Rendement 75.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #9075
alcohol
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)OC(C)(C)C)C[C@H]2Cc3ccc(CCCO)nc3N21
Reaction #12016
compound
Rendement 50.5%DOI: 10.6084/m9.figshare.5104873.v1
CN1C[C@H]2CCN(c3ccc(-c4ccc(-n5ncccc5=O)cc4)cc3)[C@H]2C1.O=C(O)[C@H](O)[C@@H](O)C(=O)O
Reaction #41236
title compound
Rendement 94.8%DOI: 10.6084/m9.figshare.5104873.v1
CN1C[C@H]2CCN(c3ccc(-c4ccc(-n5ncccc5=O)cc4)cc3)[C@H]2C1.O.O=C(O)[C@H](O)[C@@H](O)C(=O)O
Reaction #41263
2-{4′-[(3aR,6aR)-5-Methylhexahydropyrrolo[3,4-b]pyrrol-1(2H)-yl]-1,1′-biphenyl-4-yl}pyridazin-3(2H)-one L-tartrate salt monohydrate
DOI: 10.6084/m9.figshare.5104873.v1
CN1C[C@H]2CCN(c3ccc(-c4ccc(-n5ncccc5=O)cc4)cc3)[C@H]2C1.O.O=C(O)[C@H](O)[C@@H](O)C(=O)O
Reaction #41264
2-{4′-[(3aR,6aR)-5-Methylhexahydropyrrolo[3,4-b]pyrrol-1(2H)-yl]-1,1′-biphenyl-4-yl}pyridazin-3(2H)-one L-tartrate salt monohydrate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C[C@@H](OC(CC)CC)[C@H](NC(C)=O)[C@@H](N)C1.O=C(O)C(O)C(O)C(=O)O
Reaction #43885
oseltamivir tartrate
Rendement 97.6%DOI: 10.6084/m9.figshare.5104873.v1
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