بحث البنية الفرعية

537259

C[C@H]1[C@H](OCC(C)(C)C)OC[C@H]([C@@H](O)[C@@H](N)Cc2cccc(O)c2)N1C(=O)OC(C)(C)C
Reaction #48629
desired compound
المردود 104.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cccc(O)c1)[C@H](O)C1CO[C@@H](OCC(C)(C)C)[C@H](C)N1C(=O)OC(C)(C)C
Reaction #48630
desired compound
المردود 34.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1cccc(C[C@H](NC(C)=O)[C@H](O)[C@H]2CO[C@@H](OCC(C)(C)C)[C@H](C)N2C(=O)OC(C)(C)C)c1
Reaction #48631
title compound
المردود 102.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1cc(F)cc(C[C@H](NC(C)=O)[C@H](O)[C@H]2CO[C@@H](OCC(C)(C)C)[C@H](C)N2C(=O)OC(C)(C)C)c1
Reaction #48717
desired compound
المردود 47.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1[C@H](OCC(C)(C)C)OC[C@H](C(O)C(N)Cc2cc(F)cc(OCc3ccccc3)c2)N1C(=O)OC(C)(C)C
Reaction #48721
desired compound
المردود 77.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cc(O)cc(F)c1)[C@H](O)[C@H]1CO[C@@H](OCC(C)(C)C)[C@H](C)N1C(=O)OC(C)(C)C
Reaction #48722
desired compound
المردود 94.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cc(F)cc(OCC(C)C)c1)[C@H](O)[C@H]1CO[C@@H](OCC(C)(C)C)[C@H](C)N1C(=O)OC(C)(C)C
Reaction #48723
title compound
المردود 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1cc(F)cc(C[C@@H]([C@H](OCc2ccccc2)[C@H]2CO[C@@H](OCC(C)(C)CF)[C@H](C)N2C(=O)OC(C)(C)C)N(Cc2ccccc2)Cc2ccccc2)c1
Reaction #48735
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1cc(F)cc(C[C@H](NC(C)=O)[C@H](O)[C@H]2CO[C@@H](OCC(C)(C)CF)[C@H](C)N2C(=O)OC(C)(C)C)c1
Reaction #48736
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cccc(O)c1)[C@H](O)[C@H]1CO[C@@H](OCC(C)(C)C)[C@H](C)N1.O=C(O)C(F)(F)F
Reaction #48745
N-[(1S,2S)-2-[(3R,5S,6R)-6-(2,2-dimethyl-propoxy)-5-methyl-morpholin-3-yl]-2-hydroxy-1-(3-hydroxy-benzyl)-ethyl]-acetamide trifluoroacetate
DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1cc(F)cc(CC(NC(C)=O)C(O)C2COC(OCC(C)(CF)CF)C(C)N2C(=O)OC(C)(C)C)c1
Reaction #48761
5-[2-acetylamino-3-(3-fluoro-5-propoxy-phenyl)-1-hydroxy-propyl]-2-(3-fluoro-2-fluoromethyl-2-methyl-propoxy)-3-methyl-morpholine-4-carboxylic acid tert-butyl ester
المردود 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC(Cc1cc(F)cc(OCC(C)C)c1)C(O)C1COC(OCC(C)(C)C)C(C)N1C(=O)OC(C)(C)C
Reaction #208990
DOI: 10.1039/C8SC04228D
CC1C(OCC(C)(C)C)OCC(C(O)C(N)Cc2cc(F)cc(OCc3ccccc3)c2)N1C(=O)OC(C)(C)C
Reaction #225646
DOI: 10.1039/C8SC04228D
CCCOc1cc(F)cc(CC(NC(C)=O)C(O)C2COC(OCC(C)(C)CF)C(C)N2C(=O)OC(C)(C)C)c1
Reaction #908979
DOI: 10.1039/C8SC04228D
CC(=O)NC(Cc1cc(O)cc(F)c1)C(O)C1COC(OCC(C)(C)C)C(C)N1C(=O)OC(C)(C)C
Reaction #1232372
DOI: 10.1039/C8SC04228D
CCCOc1cc(F)cc(CC(NC(C)=O)C(O)C2COC(OCC(C)(CF)CF)C(C)N2C(=O)OC(C)(C)C)c1
Reaction #1305419
DOI: 10.1039/C8SC04228D
CC(=O)NC(Cc1cccc(O)c1)C(O)C1COC(OCC(C)(C)C)C(C)N1C(=O)OC(C)(C)C
Reaction #1320698
DOI: 10.1039/C8SC04228D
CCCOc1cc(F)cc(CC(NC(C)=O)C(O)C2COC(OCC(C)(C)C)C(C)N2C(=O)OC(C)(C)C)c1
Reaction #1656698
DOI: 10.1039/C8SC04228D
CCCCOc1cccc(CC(NC(C)=O)C(O)C2COC(OCC(C)(C)C)C(C)N2C(=O)OC(C)(C)C)c1
Reaction #2429681
DOI: 10.1039/C8SC04228D