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36198

CC1(C)COC(COCc2ccccc2)OC1
Reaction #59843
title compound
Ausbeute 96.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)COC(CO)OC1
Reaction #59844
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(CO)OCC2(CO1)OCCO2
Reaction #59865
title compound
Ausbeute 90.3%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(COCC2OCCCO2)cc1
Reaction #59919
title compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(COC(=O)c2ccccc2)OCCCO1
Reaction #59938
title compound
Ausbeute 66.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC1(CO)OCCCO1)c1ccccc1
Reaction #59942
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC1(CF)OCCCO1)c1ccccc1
Reaction #59943
title compound
Ausbeute 46.4%DOI: 10.6084/m9.figshare.5104873.v1
OCC1(CF)OCCCO1
Reaction #59944
title compound
Ausbeute 89.3%DOI: 10.6084/m9.figshare.5104873.v1
FC1(F)COC(COCc2ccccc2)OC1
Reaction #59948
title compound
Ausbeute 42.8%DOI: 10.6084/m9.figshare.5104873.v1
OCC1OCC(F)(F)CO1
Reaction #59949
title compound
Ausbeute 97.4%DOI: 10.6084/m9.figshare.5104873.v1
OCC1OCC2(CC2)CO1
Reaction #59989
title compound
Ausbeute 68.7%DOI: 10.6084/m9.figshare.5104873.v1
FC1(F)COC(COCc2ccccc2)OC1
Reaction #224888
DOI: 10.1039/C8SC04228D
OCC1OCC2(CC2)CO1
Reaction #260790
DOI: 10.1039/C8SC04228D
CC1(CO)OCC2(CO1)OCCO2
Reaction #382397
DOI: 10.1039/C8SC04228D
OCC1OCC(F)(F)CO1
Reaction #408162
DOI: 10.1039/C8SC04228D
c1ccc(COCC2OCC(OCc3ccccc3)CO2)cc1
Reaction #894141
DOI: 10.1039/C8SC04228D
OCC1(CF)OCCCO1
Reaction #894846
DOI: 10.1039/C8SC04228D
CCCCCC1CCC([C@H]2CO[C@H](COCc3ccccc3)OC2)CC1
Reaction #1503306
trans-2-benzyloxymethyl-5- (4-pentylcyclohexyl)-1,3-dioxane
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC1CCC([C@H]2CO[C@H](CO)OC2)CC1
Reaction #1503307
trans-[5-(4-pentylcyclohexyl)-1,3-dioxan-2-yl]methanol
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)COC(COCc2ccccc2)OC1
Reaction #1732683
title compound
Ausbeute 96.6%DOI: 10.6084/m9.figshare.5104873.v1
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