D3

CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2C3=CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #155358
7-DHC
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=C1CC[C@H](O)C/C1=C\C=C1/CCC[C@@]2(C)C1CC[C@@H]2[C@H](C)CCCC(C)C
Reaction #324165
trans-vitamin D3
Ausbeute 61.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_06
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4CC(N5C(=O)c6ccccc6C5=O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #353188
3-phthalimidocholestane
Ausbeute 81.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4CC(N5C(=O)c6ccccc6C5=O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #444029
3-phthalimidocholestane
Ausbeute 81.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4CC(N5C(=O)c6ccccc6C5=O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #704355
3-phthalimidocholestane
Ausbeute 81.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4CC(N5C(=O)c6ccccc6C5=O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #949593
3-phthalimidocholestane
Ausbeute 81.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_02
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4CC(N5C(=O)c6ccccc6C5=O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1051210
3-phthalimidocholestane
Ausbeute 81.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_06
CC1=C(/C=C\C2=CCC[C@]3(C)[C@@H]([C@H](C)CCCC(C)C)CC[C@@H]23)C[C@@H](O)CC1
Reaction #1164561
previtamin D3
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_08
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4CC(N5C(=O)c6ccccc6C5=O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1376271
3-phthalimidocholestane
Ausbeute 81.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_05
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4CC(N5C(=O)c6ccccc6C5=O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1503054
3-phthalimidocholestane
Ausbeute 81.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_06
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4CC(N5C(=O)c6ccccc6C5=O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1507727
3-phthalimidocholestane
Ausbeute 81.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_06
C=C1CC[C@H](O)C/C1=C/C=C1\CCC[C@]2(C)[C@@H]([C@H](C)/C=C/[C@H](C)C(C)C)CC[C@@H]12
Reaction #1533982
Vitamin D2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_02
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4CC(N5C(=O)c6ccccc6C5=O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1672688
3-phthalimidocholestane
Ausbeute 81.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_08
COc1ccc(COCc2ccc(OC)cc2)cc1
Reaction #1675160
p-methoxybenzyl ether
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_06
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](OC(=O)c5ccccc5)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1808485
3β-Benzoyloxy-5α-Cholestane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_04
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1808710
5α-cholestan-3-one
Ausbeute 89.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_04
CC[Si](CC)(CC)OC1CC[C@@]2(C)C(=CC=C3[C@@H]4CC[C@H]([C@@H](C)CCCC(C)C)[C@@]4(C)CC[C@@H]32)C1
Reaction #1934287
title compound
Ausbeute 87.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_02
COCOC1CC[C@@]2(C)C(=CC=C3[C@@H]4CC[C@H]([C@H](C)CCCC(C)C)[C@@]4(C)CC[C@@H]32)C1
Reaction #1934288
title compound
Ausbeute 85.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_02
COCOC1CC[C@@]2(C)C(=CC=C3[C@@H]4CC[C@H]([C@@H](C)CCCC(C)C)[C@@]4(C)CC[C@@H]32)C1
Reaction #1934303
(S)-3-methoxymethoxy-5,7-cholestadiene
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_02
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4CC(N5C(=O)c6ccccc6C5=O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #2021488
3-phthalimidocholestane
Ausbeute 81.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_05
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