Ähnlichkeitssuche

322161

O=C(N[C@@H](Cc1ccccc1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)OCc1ccccc1
Reaction #80965
desired compound
Ausbeute 58.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCNC[C@@H](O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1
Reaction #81939
N[3(S)-benzyloxycarbonylamino-2(R)-hydroxy-4-phenylbutyl]N-isoamylamine
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCNC[C@@H](O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1
Reaction #82516
N[3(S)-benzyloxycarbonylamino-2(R)-hydroxy-4-phenylbutyl]N-isoamylamine
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(Cc1ccccc1)CC(O)C(Cc1ccccc1)NC(=O)OCc1ccccc1)OCc1ccccc1
Reaction #193187
DOI: 10.1039/C8SC04228D
O=C1NC(Cc2ccccc2)C(CO)O1
Reaction #197583
DOI: 10.1039/C8SC04228D
CC(C)CCC(CC(O)C(Cc1ccccc1)NC(=O)OCc1ccccc1)S(=O)(=O)c1ccccc1
Reaction #201775
DOI: 10.1039/C8SC04228D
O=C(NC(Cc1ccccc1)CC(O)C(Cc1ccccc1)NC(=O)OCc1ccccc1)OCc1ccccc1
Reaction #289355
DOI: 10.1039/C8SC04228D
CC(C)CCC(CC(O)C(Cc1ccccc1)NC(=O)c1cnc2ccccc2n1)S(=O)(=O)c1ccccc1
Reaction #395530
DOI: 10.1039/C8SC04228D
CC(C)CCNC[C@@H](O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1
Reaction #462152
N[3(S)-benzyloxycarbonylamino-2(R)-hydroxy-4-phenylbutyl]N-isoamylamine
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccccc1)[C@H]1CO1)OCc1ccccc1
Reaction #463168
N-benzyloxycarbonyl-3(S)-amino-1,2(S)-epoxy-4-phenylbutane
Ausbeute 86.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccccc1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)OCc1ccccc1
Reaction #520923
desired compound
Ausbeute 58.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccccc1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)OCc1ccccc1
Reaction #530288
desired compound
Ausbeute 58.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCNC[C@@H](O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1
Reaction #813084
N[3(S)-benzyloxycarbonylamino-2(R)-hydroxy-4-phenylbutyl]N-isoamylamine
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccccc1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)OCc1ccccc1
Reaction #829304
desired compound
Ausbeute 58.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccccc1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)OCc1ccccc1
Reaction #831932
desired compound
Ausbeute 58.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccccc1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)OCc1ccccc1
Reaction #937703
desired compound
Ausbeute 58.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(Cc2ccccc2)C(CO)O1
Reaction #1019548
DOI: 10.1039/C8SC04228D
O=C(N[C@@H](Cc1ccccc1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)OCc1ccccc1
Reaction #1062722
desired compound
Ausbeute 58.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccccc1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)OCc1ccccc1
Reaction #1063252
desired compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCNC[C@@H](O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1
Reaction #1063299
N[3(S)-benzyloxycarbonylamino-2(R)-hydroxy-4-phenylbutyl]N-isoamylamine
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
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