cholesterol

CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@](O)(C(=O)OCCl)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1502
3-(Chloromethoxycarbonyl) Cholesterol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #66034
H+
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@H](N=[N+]=[N-])CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92529
3α-azidocholest-5-ene
收率 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)CCC1CO1
Reaction #304176
Glycidyl cholesterol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)CCC1CO1
Reaction #304177
glycidyl-cholesterol
收率 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](OS(C)(=O)=O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #306478
product
收率 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CCCCCCCC/C=C\CCCCCCCC(=O)[O-].[Na+]
Reaction #310878
sodium oleate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_10
CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCCCC
Reaction #317783
cetyl stearate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@H]1C[C@H](N)[C@@H](O)[C@H](C)O1.Cl
Reaction #336416
Epirubicin HCl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
—
Reaction #356890
hydrogenated phosphatidylcholines
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](Br)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #366009
Cholesteryl Bromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CCCCCCCC/C=C\CCCCCCCC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4CC[C@H]([C@H](C)CCCC(C)C)[C@@]4(C)CC[C@@H]32)C1
Reaction #448877
cholesteryl oleate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
N[C@H](C(=O)O)[C@H](O)c1ccc(O)c(O)c1
Reaction #495239
DOPS
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](Br)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #516884
Cholesteryl Bromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3C=CC4=CC(=O)C=C[C@]4(C)[C@H]3CC[C@]12C
Reaction #531591
1,4,6-cholestatrien-3 one
收率 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_04
CC(CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)CC(=O)CBr
Reaction #556360
Bromoacetyl-Cholesterol
收率 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CCc1cccc(CC)c1N(COC)C(=O)CCl
Reaction #568462
Alachlor
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_08
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](OC(=O)c5cc([N+](=O)[O-])cc([N+](=O)[O-])c5)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #598914
(3-β)-cholest-5-en-3-yl 3,5-dinitrobenzoate
收率 56.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](OS(C)(=O)=O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #639192
product
收率 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C.Cc1cc2c(s1)Nc1ccccc1N=C2N1CCN(C)CC1
Reaction #651876
Olanzapine Cholesterol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
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