Teilstruktursuche

803795

—
Reaction #40485
solid
DOI: 10.6084/m9.figshare.5104873.v1
CC(O)[C@H]1COC[C@@H](c2ccc(F)c(F)c2)N1C(=O)OCC1c2ccccc2-c2ccccc21
Reaction #44663
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(O)[C@H]1COC[C@@H](c2ccc(F)c(F)c2)N1
Reaction #44664
titled compound
Ausbeute 85.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1COC[C@@H](c2cc(F)c(F)c(F)c2)N1C(=O)OCc1ccccc1
Reaction #44666
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[C@H]1COC[C@@H](c2cc(F)c(F)c(F)c2)N1C(=O)OCc1ccccc1
Reaction #44667
titled compound
Ausbeute 91.4%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)CN1C(=O)OC(C)(C)C
Reaction #48615
title compound
Ausbeute 99.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](OCc1ccccc1)[C@H]1CO[C@H](OCCCC2CCCC2)CN1.O=C(O)C(F)(F)F
Reaction #48616
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)OC[C@H]1CN(C(=O)OC(C)(C)C)[C@@H]([C@@H](O)[C@@H](N)Cc2cc(F)cc(F)c2)CO1
Reaction #48621
desired compound
Ausbeute 100.2%DOI: 10.6084/m9.figshare.5104873.v1
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
Ausbeute 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
Ausbeute 34.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC[C@H]1CN(C(=O)OC(C)(C)C)[C@@H]([C@@H](O)[C@@H](N)Cc2cc(F)cc(F)c2)CO1
Reaction #48634
desired compound
Ausbeute 93.0%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](CCC(C)C)CN1C(=O)OC(C)(C)C
Reaction #48635
5-(S)-[2-(R)-Acetylamino-3-(3,5-difluorophenyl)-1-(R)-hydroxypropyl]-2-(S)-(3-methylbutyl)-morpholine-4-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CO[C@H]1CN(C(=O)OC(C)(C)C)[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(Cl)c2)[N+](=O)[O-])CO1
Reaction #48639
desired compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CO[C@H]1CN(C(=O)OC(C)(C)C)[C@@H]([C@@H](O)[C@@H](N)Cc2cc(F)cc(Cl)c2)CO1
Reaction #48640
desired compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cc(F)cc(Cl)c1)[C@H](O)[C@H]1CO[C@@H](OCC(C)(C)C)CN1C(=O)OC(C)(C)C
Reaction #48641
title compound
Ausbeute 45.5%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](CCC2CCCCC2)CN1C(=O)OC(C)(C)C
Reaction #48644
title compound
Ausbeute 37.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](CCC2CCCCC2)OC[C@@H]1[C@@H](O)[C@H](Cc1ccccc1)[N+](=O)[O-]
Reaction #48648
desired compound
Ausbeute 63.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](CCC2CCCCC2)OC[C@@H]1[C@@H](O)[C@@H](N)Cc1ccccc1
Reaction #48649
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1ccccc1)[C@H](O)[C@H]1CO[C@@H](CCC2CCCCC2)CN1C(=O)OC(C)(C)C
Reaction #48650
title compound
Ausbeute 54.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](CO)OC[C@@H]1[C@@H](O)[C@@H](N)Cc1cc(F)cc(F)c1
Reaction #48656
desired compound
Ausbeute 88.3%DOI: 10.6084/m9.figshare.5104873.v1
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