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C=CC1CCC2OC2C1

CC(=O)OCC(=O)C1=CCC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(O)CC12C
Reaction #266232
DOI: 10.1039/C8SC04228D
C=C(C)[C@H]1CC[C@@](C)(O)[C@H](N[C@@H](C)C2CCCCC2)C1
Reaction #366672
(1R,2R,4S)-2-((1S)-1-cyclohexylethylamino)-1-methyl-4-(1-methylethenyl) cyclohexanol
Ausbeute 33.7%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@H]1CC[C@@](C)(O)[C@H](NC23CC4CC(CC(C4)C2)C3)C1
Reaction #366673
(1R,2R,4S)-2-(1-adamantylamino)-1-methyl-4-(1-methylethenyl)cyclohexanol
Ausbeute 39.8%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@](C)(O)[C@@H](n2ccnc2)C1
Reaction #366674
(+)-(1S,2S,4R)-2-(1-Imidazolyl)-1-methyl-4-(1-methylethenyl)cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1=C2C3OC3C3C(CCC4(C)C(=O)CCC34)C2(C)C=CC1=O
Reaction #401035
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](O[C@@H]1C[C@H](O)C[C@H]2O[C@]21C)(c1ccccc1)c1ccccc1
Reaction #475918
title compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@H]1C[C@@H]2O[C@]2(C)[C@H](O[Si](C)(C)C(C)(C)C)C1
Reaction #475925
titled compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@H]1CC(=O)[C@]2(C)O[C@@H]2C1
Reaction #475936
(1R,4R,6R)-4-Isopropenyl-1-methyl-7-oxabicyclo[4.1.0]heptan-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@]12O[C@H]1[C@@H]1O[C@]13[C@]1(O[C@H]1C[C@H]1C4=C(CC[C@@]13C)C(=O)OC4)[C@H]2F
Reaction #583489
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C=CC1CCC(O)C(OC(=O)CCCCCCC(=O)OC2CC(C=C)CCC2O)C1
Reaction #642972
Bis(2-hydroxy-5-vinyl-cyclohexyl)Suberate
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C1CCC2(C)OC2C1
Reaction #736302
Limonene Oxide
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #790436
13
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)OC1CC(CC)CCC1OC(=O)CCC(=O)O
Reaction #1018586
4-((2-(acryloyloxy)-4-ethylcyclohexyl)oxy)-4-oxobutanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=CC1CCC(O)C(O)C1
Reaction #1094808
1,2-dihydroxy-4-vinylcyclohexane
DOI: 10.6084/m9.figshare.5104873.v1
CO[Si](CCC1CCC2OC2C1)(OC)OC
Reaction #1307109
DOI: 10.1039/C8SC04228D
CC(=O)NC1=C2C(F)C(O)C3C(CCC4(C)C(=O)CCC34)C2(C)C=CC1=O
Reaction #1310120
DOI: 10.1039/C8SC04228D
CC1([C@H]2CC=C3[C@@H]4CC5OC56C[C@@H](O)CC[C@]6(C)[C@H]4C[C@@H](O)[C@@]32C)OCCO1
Reaction #1461964
3β,12β-Dihydroxy-5,6-epoxy-20,20-ethylenedioxypregn-14-ene
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@]12O[C@H]1[C@@H]1O[C@]13[C@]1(O[C@H]1C[C@H]1C4=C(CC[C@@]13C)C(=O)OC4)[C@@H]2O.O=C([O-])CCC(=O)[O-]
Reaction #1463901
triptolide succinate
Ausbeute 136.2%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@](C)(O)[C@@H](Sc2ccccc2)C1
Reaction #1475992
thioether
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C1CCC(C)(O)C(N2CCOCC2)C1
Reaction #1519695
product
Ausbeute 49.5%DOI: 10.6084/m9.figshare.5104873.v1
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