Recherche de Sous-structure

3638

COc1cccc(C(=O)N(CCOC2CCCCO2)c2ccccc2OC)c1
Reaction #2558
title compound
Rendement 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C(=O)N(CCO)c2ccccc2OC)c1
Reaction #2559
title compound
Rendement 86.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](OCc1ccccc1)[C@@H](COC(CI)OCCC(C)(C)C)NC(=O)OC(C)(C)C
Reaction #48614
title compound
Rendement 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(C)=O)CO1.O=C(O)C(F)(F)F
Reaction #48753
title compound
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](O)[C@H]1CO[C@@H](OCCC(C)(C)C)CN1.O=C(O)C(F)(F)F
Reaction #48754
title compound
Rendement 98.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](O)[C@H]1CO[C@@H](OCC(C)(C)C)[C@H](C)N1.Cl
Reaction #48757
title compound
Rendement 45.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](O)[C@H]1CO[C@@H](OCC(C)(C)C)[C@H](C)N1.Cl
Reaction #48758
title compound
Rendement 65.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC(Cc2ccc(OC)cc2)N2C(=O)[C@H]([C@@H](C)OC(=O)OCc3ccccc3)[C@H]2C(C)(C)O)cc1
Reaction #49992
(3S,4S)-4-(1-hydroxy-1-methylethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinone
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(=O)CC[C@@H]1[C@@H](CC(=O)C(F)CCCC(=O)OC)[C@@H](OC2CCCCO2)C[C@H]1OC1CCCCO1
Reaction #50192
title compound ( 55 )
DOI: 10.6084/m9.figshare.5104873.v1
CSc1nnc2n1C=Cc1ccccc1C2C
Reaction #54784
11-methyl-3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine
DOI: 10.6084/m9.figshare.5104873.v1
CC(O)(C#CCCO)c1ccc(-c2ccc(Cl)cc2)cc1
Reaction #54991
2-(4'-chloro-4-biphenylyl)-3-hexyn-2,6-diol
DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)ON(C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)O[C@H]1CO[C@H]2OCC[C@H]21)S(=O)(=O)c1ccc(N)cc1
Reaction #57492
(3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl (1S,2R)-3-[[(4-aminophenyl)sulfonyl](1-ethylpropoxy)amino]-1-benzyl-2-hydroxypropylcarbamate
Rendement 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)ON(C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)O[C@H]1CO[C@H]2OCC[C@H]21)S(=O)(=O)c1cccc(N)c1
Reaction #57494
(3R,3aS,6aR)hexahydrofuro[2,3-b]furan-3-yl (1S,2R)-3-[[(3-aminophenyl)sulfonyl](1-ethylpropoxy)amino]-1-benzyl-2-hydroxypropylcarbamate
Rendement 67.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)COC(c2ccccc2-c2ccc(COC3CCCCO3)cc2)=N1
Reaction #81701
title compound
Rendement 53.0%DOI: 10.6084/m9.figshare.5104873.v1
OCCn1cc(-c2cncc(-c3ccnc(-c4ccccc4F)c3)n2)cn1
Reaction #171358
2-(4-{6-[2-(2-fluoro-phenyl)-pyridin-4-yl]-pyrazin-2-yl}-pyrazol-1-yl)-ethanol
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NCCN3CCS(=O)(=O)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O[C@H]7O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]7O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172893
desired product
Rendement 52.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(NS(=O)(=O)c2ccc3c(c2)OCO3)c(Oc2ccccc2OC)c(OCCOC2CCCCO2)c1
Reaction #174379
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(NS(=O)(=O)c2ccc(C(C)(C)C)cc2)c(Oc2cc(OC)ccc2Cl)c(OCCOC2CCCCO2)c1
Reaction #178977
DOI: 10.1039/C8SC04228D
O=C(NOCCO)c1ccc(F)c(F)c1Nc1ccc(C#CCOC2CCCCO2)cc1F
Reaction #183434
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(CCOCOCc2ccccc2)cc1)C(F)(F)F
Reaction #187243
DOI: 10.1039/C8SC04228D
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