Teilstruktursuche

510056

CC(CO)CCCC(C)C1C(=O)CC2C3CC=C4CC(O)CCC4(C)C3CCC21C
Reaction #231108
DOI: 10.1039/C8SC04228D
C[C@H](CCC[C@@H](C)[C@H]1C(=O)C[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)CN1C(=O)c2ccccc2C1=O
Reaction #414951
compound ( 5 )
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CCC[C@@H](C)[C@H]1C(=O)C[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)CN1C(=O)c2ccccc2C1=O
Reaction #414952
(25R)-16-oxo-26-phthalimidocholesterol
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CO)CCC[C@@H](C)[C@H]1C(=O)C[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #414955
(25R)-16-oxo-26-hydroxycholesterol
Ausbeute 62.9%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CO)CCC[C@@H](C)[C@H]1[C@@H](O)C[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #414956
(25R)-16β, 26-dihydroxycholesterol
Ausbeute 160.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OCC(C)CCCC(C)C2C(=O)CC3C4CC=C5CC(O)CCC5(C)C4CCC32C)cc1
Reaction #2242919
DOI: 10.1039/C8SC04228D