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CCCCCCCCC=CCCCCCCCC

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

Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1

—

Reaction #4256

heterocyclic compound

DOI: 10.6084/m9.figshare.5104873.v1

Reaction #5232

Octadec-9-enoyl chloride

Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1

—

Reaction #7423

final solution

DOI: 10.6084/m9.figshare.5104873.v1

$CCCCCCCC/C=C\CCCCCCCC(=O)OCC$

Reaction #42009

ethyl oleate

Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1

$CCCCCCCC/C=C\CCCCCCCC(=O)OCC$

Reaction #42010

ethyl oleate

Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1

$CCCCCCCC/C=C\CCCCCCCC(=O)OCCCCC$

Reaction #42011

pentyl oleate

Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1

$CCCCCCCC/C=C\CCCCCCCC(=O)NCC(=O)O$

Reaction #53625

N-Oleoyl glycine

DOI: 10.6084/m9.figshare.5104873.v1

$CCCCCCCC/C=C\CCCCCCCCOCC(CN(C)C)OCCCCCCCC/C=C\CCCCCCCC$

Reaction #82857

title compound

Ausbeute 72.6%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

$CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCC/C=C\CCCCCCCC.CCCCCCCC/C=C\CCCCCCCCOCC(C[N+](C)(C)C)OCCCCCCCC/C=C\CCCCCCCC.[Cl-]$

Reaction #82860

DOTMA DOPC

DOI: 10.6084/m9.figshare.5104873.v1

$CCCCCCCC/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCC/C=C\CCCCCCCC.CCCCCCCC/C=C\CCCCCCCCOCC(C[N+](C)(C)C)OCCCCCCCC/C=C\CCCCCCCC.[Cl-]$

Reaction #82861

DOTMA DOPC

DOI: 10.6084/m9.figshare.5104873.v1

—

Reaction #82863

DOTMA

DOI: 10.6084/m9.figshare.5104873.v1