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C=CC(C)CCO

CC(=O)OCC(=O)[C@@]1(O[Si](C)(C)C)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O[Si](C)(C)C)C[C@@]21C
Reaction #42650
title compound
Ausbeute 103.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC(=O)[C@@]1(O)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O[Si](C)(C)C)C[C@@]21C
Reaction #42651
title compound
Ausbeute 73.9%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](NC(=O)O[C@]1(C(=O)CO)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@@]21C)c1ccccc1
Reaction #42655
(11β,16β)-9-fluoro-11,21-dihydroxy-16-methyl-3,20-dioxopregna-1,4-dien-17-yl (1R)-1-phenylethylcarbamate
Ausbeute 57.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCNC(=O)O[C@]1(C(=O)CO)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@@]21C
Reaction #42656
title compound
Ausbeute 60.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(O)C1CCCCCC=C1Br
Reaction #74254
17
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(O)C1C#CCCCCC1
Reaction #74255
cyclooct-1-yn-3-glycolic acid
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(=O)O[C@]1(C(=O)C(O)OC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)C)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@@]21C
Reaction #81347
(2S)-2-((1,1-dimethylethoxycarbonyl)-amino)-3-methyl-butyric acid [11β,21-dihydroxy-3,20-dioxo-9-fluoro-16β-methyl-17-valeroyloxy-pregna -1,4-dien-21-yl] ester
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(CC(=O)O)c1ccc(Cl)c(Cl)c1
Reaction #195806
DOI: 10.1039/C8SC04228D
C=C(COC1CC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(O)CC2(C)C1(O)C(=O)CCl)c1ccccc1
Reaction #199533
DOI: 10.1039/C8SC04228D
C=C(COC1CC2C3CCC4=CC(=O)CCC4(C)C3(F)C(O)CC2(C)C1(O)C(=O)CO)c1ccccc1
Reaction #200009
DOI: 10.1039/C8SC04228D
CCCNC(=O)OC1(C(=O)CO)C(C)CC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(O)CC21C
Reaction #203830
DOI: 10.1039/C8SC04228D
CC12C=CC(=O)C=C1C(F)CC1C3CC4CN(Cc5ccccc5)CC4(C(=O)SC4CCOC4=O)C3(C)CC(O)C12F
Reaction #207496
DOI: 10.1039/C8SC04228D
CC(=O)OC1CC2(C)C(=O)CCC2C2CCC3=CC(=O)C=CC3(C)C12F
Reaction #212457
DOI: 10.1039/C8SC04228D
CCCCCC(C=CC1C(OC2CCCCO2)CC2OC(C(Br)CCCC(=O)OC)CC21)OC1CCCCO1
Reaction #213779
DOI: 10.1039/C8SC04228D
COC(=O)OC1CC2=CC=C3C4CCC(C(C)CS(=O)c5ccccc5)C4(C)CCC3C2(C)C(OC(=O)OC)C1
Reaction #222886
DOI: 10.1039/C8SC04228D
CCSC1=CCC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(OC(C)=O)CC12C
Reaction #224915
DOI: 10.1039/C8SC04228D
CCSC1(SC)CCC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(OC(C)=O)CC21C
Reaction #226821
DOI: 10.1039/C8SC04228D
CC1CC2C3CCC4=CC(=O)CCC4(C)C3(F)C(O)CC2(C)C1(O)C(=O)CO
Reaction #254862
DOI: 10.1039/C8SC04228D
COC(=O)C(O)C1CCCCCC=C1Br
Reaction #266216
DOI: 10.1039/C8SC04228D
C=CC1CC1(NC(=O)C1CC(Oc2nccc3cc(OC)ccc23)CN1C(=O)C(NC(=O)OC(C)(C)C)C1CCCCC1)C(=O)OC
Reaction #281236
DOI: 10.1039/C8SC04228D
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