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CC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4CC[C@H]([C@H](C)CCC(=O)C(C)C)[C@@]4(C)CC[C@@H]32)C1
Reaction #3186
3β-acetoxy-24-oxo-5-cholestene
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC/C=C\CC[C@@H](C[C@@H]1OC(=O)[C@H]1CCCCCC)OC(=O)[C@H](CC(C)C)NC=O
Reaction #6160
N-formyl-L-leucine (S,Z)-1-[[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl]methyl]-4-dodecenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC(c2ccccc2)C(CO)NC(=O)CCCCCNC(=O)OC2CCC3(C)C(=CCC4C3CCC3(C)C(C(C)CCCC(C)C)CCC43)C2)c2ccc(OC)cc2)cc1
Reaction #49186
crude product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCC1CCCCCCCCCCC1)C1=C(O)CSC1=O
Reaction #65586
white solid
Выход 33.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC/C=C\CCCCCCCCCC(CO)CCCCCCCC/C=C\CCCCCCCC
Reaction #82859
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@H](N)CC[C@]4(C)[C@H]3CC[C@]12C.O=C(O)CC(O)(CC(=O)O)C(=O)O
Reaction #92532
3α-aminocholest-5-ene citrate
Выход 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2C3=C[C@@H](NCCCNCCCCN)[C@@]4(O)C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92660
Dendrogenin B
Выход 58.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #92667
solid
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2C3=C[C@@H](NCCCN)[C@@]4(O)C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92668
5α-Hydroxy-6β-(3-aminopropylamino)-cholest-7-en-3β-ol
Выход 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN[C@@H]1C=C2[C@@H]3CC[C@H]([C@H](C)CCCC(C)C)[C@@]3(C)CC[C@@H]2[C@@]2(C)CC[C@H](O)C[C@]12O
Reaction #92669
5α-Hydroxy-6β-(3-propylamino)-cholest-7-en-3β-ol
Выход 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCC=CC1CC(=O)NC1=O
Reaction #93456
eicosenyl succinimide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1CC2=CCC3C4CCC(C(C)CCC=O)C4(C)CCC3C2(C)C(OC(C)=O)C1
Reaction #174830
DOI: 10.1039/C8SC04228D
CC(=O)OC1CCC2C(=CC(C)C3C2CCC2(C)C(O)CCC32)C1
Reaction #183087
DOI: 10.1039/C8SC04228D
C=CCC(O)CCCCCCCCCCCCCCCCC
Reaction #213172
DOI: 10.1039/C8SC04228D
CC(=O)O[C@H]1C[C@H](O)CC2=CC[C@H]3[C@@H]4CC[C@H]([C@H](C)CCCC(C)C)[C@@]4(C)CC[C@@H]3[C@]21C
Reaction #213852
1α-acetoxycholesterol
Выход 107.8%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #215382
oil
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCC1CCCCCCCCCCC1)C1=C(O)CSC1=O
Reaction #216717
white solid
Выход 33.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCCC(C)C1CCC2C3CC=C4CC(OC(=O)NCC(=O)ON5C(=O)CCC5=O)CCC4(C)C3CCC12C
Reaction #225873
DOI: 10.1039/C8SC04228D
CCCCC(=O)OC1(C(=O)COC(C)=O)CCC2C3CC(C)C4=CC(=O)CCC4(C)C3C(O)CC21C
Reaction #236714
DOI: 10.1039/C8SC04228D
[Na+]
Reaction #241056
DOI: 10.1039/C8SC04228D
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