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1281320

CCCC(CCC)C(=O)OCCC(=O)OC1COC(c2ccccc2)OC1
Reaction #70093
solid
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(CCC)C(=O)OCCC(=O)OC(CO)CO
Reaction #70094
clear oil
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1COc2c(N3CCN(C)CC3)c(F)cc3c(=O)c(C(=O)OC(CO)CO)cn1c23
Reaction #70098
yellow gum
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)OC1COC(c2ccccc2)OC1
Reaction #70099
2-phenyl-1,3-dioxan-5-yl carbonochloridate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCC(=O)OC(CO)CO)Oc1ccccc1
Reaction #70105
1,3-dihydroxypropan-2-yl phenyl succinate
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)c2cc(OC3COC(c4ccccc4)OC3)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Reaction #89982
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)c2cc(OC(CO)CO)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Reaction #89983
title compound
Ausbeute 66.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(C2OCC(OCc3ccccc3)CO2)c1
Reaction #175400
DOI: 10.1039/C8SC04228D
CCCC(CCC)C(=O)OCCC(=O)OC(CO)CO
Reaction #180404
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCNc1ccc(CCC(=O)OC(CO)CO)cc1
Reaction #186030
DOI: 10.1039/C8SC04228D
OC1COC(c2ccccc2)OC1
Reaction #198249
DOI: 10.1039/C8SC04228D
Cc1cccc(C2OCC(O)CO2)c1
Reaction #199633
DOI: 10.1039/C8SC04228D
COCc1c(C(=O)OC(CO)CO)ncc2[nH]c3ccc(OCc4ccccc4)cc3c12
Reaction #201066
DOI: 10.1039/C8SC04228D
c1ccc(COC2COC(c3ccccc3)OC2)cc1
Reaction #232906
DOI: 10.1039/C8SC04228D
OC1COC(c2ccc(Cl)cc2)OC1
Reaction #257934
DOI: 10.1039/C8SC04228D
CC(C)Oc1cc(OC(CO)CO)ccc1OC(=O)c1ccccc1
Reaction #278718
DOI: 10.1039/C8SC04228D
COC(CO)COCc1ccccc1
Reaction #283216
DOI: 10.1039/C8SC04228D
CCOc1ccccc1C1OCC(O)CO1
Reaction #290864
DOI: 10.1039/C8SC04228D
[N-]=[N+]=NC1COC(c2ccccc2)OC1
Reaction #295522
DOI: 10.1039/C8SC04228D
OC1COC(c2ccccc2)OC1
Reaction #322876
desired title compound
Ausbeute 21.1%DOI: 10.6084/m9.figshare.5104873.v1
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