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303668

$C/C(=C\[C@H]1CC[C@H](O[Si](C)(C)C(C)(C)C)CC1)C(O)CCCc1ccccc1$

Reaction #978

alcohol

DOI: 10.6084/m9.figshare.5104873.v1

Reaction #1109

4-[4-(3-Cyclohexylpropylidene)cyclohexylamino]-3-ethoxy-2-methylpyridine

Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1

$CCCCCCCC/C=C\CCCCCCCCNC(=O)OC(CCCO)COC/C=C(\C)CCC=C(C)C$

Reaction #5350

(Z)-9-octadecenylcarbamic acid (E)-1-[[(3,7-dimethyl-2,6-octadienyl)oxy]methyl]-4-hydroxybutyl ester

Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)CCCCCC[C@H]1C2OCCOC2C[C@@H]1CCC(=O)CCC=C(C)C

Reaction #55563

9-ethylenedioxy-15-keto-19-methyl-prost-18-enoic acid, methyl ester

Ausbeute 88.2%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #55564

9-ethylenedioxy-15-keto-19-methyl-prost-18-enoic acid, methyl ester

Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1

CCCCC[C@@H](/C=C/[C@@H]1[C@@H](Cc2cccc(OCc3ccccc3)c2)[C@@H](COS(=O)(=O)c2ccc(C)cc2)C[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C

Reaction #67889

((1S,2S,3R,4R)-2-(3-(benzyloxy)benzyl)-4-(tert-butyldimethylsilyoxy)-3-((S,E)-3-(tert-butyldimethylsilyoxy)oct-1-enyl)cyclopentyl)methyl 4-methylbenzenesulfonate

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

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

Reaction #82862

DOPG DOPC

DOI: 10.6084/m9.figshare.5104873.v1

$CCNC(=O)CCC/C=C\C[C@@H]1[C@@H](/C=C/[C@@H](O)CCc2ccccc2)[C@H](O)C[C@@H]1O.NC(CO)(CO)CO$

Reaction #90845

Bimatoprost Tromethamine

DOI: 10.6084/m9.figshare.5104873.v1

CC(C)CCC(=O)[C@@]1(O)C(O)=C(C(=O)CC(C)C)C(=O)[C@@H]1CCC(C)C

Reaction #160560

(+)-KDT-500

DOI: 10.6084/m9.figshare.5104873.v1

C=CC=CC(C)C(O)C(C)C(CCC(C)CC(C)C(O[Si](C)(C)C(C)(C)C)C(C)C=CC(CC(O[Si](C)(C)C(C)(C)C)C(C)C=CC=CC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C

Reaction #182322

DOI: 10.1039/C8SC04228D

CC(C)=CCCC(=O)CCC1CC2OCCOC2C1CCCCCCC(=O)O

Reaction #211114

DOI: 10.1039/C8SC04228D

—

Reaction #215383

syrup

Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)OC(=O)NC1CCCCCC=CC2CC2(C(=O)NS(=O)(=O)C2CC2)NC(=O)C2CC(OC(=O)c3ccc4c(c3)OCO4)CN2C1=O

Reaction #241374

DOI: 10.1039/C8SC04228D

C=C(C)OC(=O)OC1C(C)=CC2C(C(C)C)CCC(C)C2(O)C1OC(=O)C1CC2(O)c3cccc(Cl)c3N(C)OC2N1

Reaction #248949

DOI: 10.1039/C8SC04228D

CCC(O[Si](CC)(CC)CC)C(C)C1OC1CC(C)(C=CC=C(C)C1OC(=O)CC(O[Si](CC)(CC)CC)CCC(C)C(O)C=CC1C)O[Si](CC)(CC)CC

Reaction #257813

DOI: 10.1039/C8SC04228D

Reaction #263046

DOI: 10.1039/C8SC04228D

CCCCCC(O)C=CC1C=C(Cl)C(=O)C1=Cc1cccc(OC(C)C(=O)OC)c1

Reaction #263880

DOI: 10.1039/C8SC04228D

CCCCCCCCCCC1C(O)CC(O)C1CC=CCCCCCC(=O)OC(C)C

Reaction #271702

DOI: 10.1039/C8SC04228D

CCCCC(C)CC(C=CC1C(SCCCCCC(=O)OC)=C(C(=O)OC)CC1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C

Reaction #271927

DOI: 10.1039/C8SC04228D

CCCCCC(O)C=CC1C=C(S(C)=O)C(=O)C1C(O)CCCCCC(=O)OC

Reaction #273895

DOI: 10.1039/C8SC04228D

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