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OCc1ccc2c(c1)OCO2

COC(=O)c1cc(Cl)c2c(c1Cl)OC(c1ccccc1)(c1ccccc1)O2
Reaction #299855
DOI: 10.1039/C8SC04228D
COc1cc(C(=O)O)c(-c2c(C(=O)O)cc(OC)c3c2OCO3)c(OC)c1OC
Reaction #319029
2',3'-methylenedioxy-2,3,4,4'-tetramethoxy-1,1'-biphenyl-6,6'-dicarboxylic acid
Ausbeute 92.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1c(OC)cc(C(=O)O)c(-c2c(C(=O)O)cc(OC)c3c2OCO3)c1OCC
Reaction #319030
2,3-diethoxy-4,4'-dimethoxy-2',3'-methylenedioxy-1,1'-biphenyl-6,6'-dicarboxylic acid
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1c(OC)c(OC)cc(C(=O)O)c1-c1c(C(=O)O)cc(OC)c2c1OCO2
Reaction #319031
2-ethoxy-2',3'-methylenedioxy-3,4,4'-trimethoxy-1,1'-biphenyl-6,6'-dicarboxylic acid
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #321528
yellow solid
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #321529
light orange solid
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2c(C(C)(O)c3ccc4c(c3)OCO4)nc(N)nc2s1
Reaction #324578
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
OCc1ccc2c(c1)OC(F)(F)O2
Reaction #329311
(2,2-difluoro-1,3-benzodioxol-5-yl)-methanol
DOI: 10.6084/m9.figshare.5104873.v1
FC1(F)Oc2ccc(CCl)cc2O1
Reaction #329312
5-chloromethyl-2,2-difluoro-1,3-benzodioxole
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)O)c(-c2c(C(=O)O)cc(OC)c3c2OCO3)c(OC)c1OC
Reaction #345336
2',3'-methylenedioxy-2,3,4,4'-tetramethoxy-1,1'-biphenyl-6,6'-dicarboxylic acid
Ausbeute 92.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1c(OC)cc(C(=O)O)c(-c2c(C(=O)O)cc(OC)c3c2OCO3)c1OCC
Reaction #345337
2,3-diethoxy-4,4'-dimethoxy-2',3'-methylenedioxy-1,1'-biphenyl-6,6'-dicarboxylic acid
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1c(OC)c(OC)cc(C(=O)O)c1-c1c(C(=O)O)cc(OC)c2c1OCO2
Reaction #345338
2-ethoxy-2',3'-methylenedioxy-3,4,4'-trimethoxy-1,1'-biphenyl-6,6'-dicarboxylic acid
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
C(=COCc1ccc2c(c1)OCO2)CCCCCCCC1CO1
Reaction #354546
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CSCCCCCCCCCCCCOCc1ccc2c(c1)OCO2
Reaction #354547
13-thiatetradecyl piperonyl ether
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(O)(c2ccc3c(c2)OCO3)CC1
Reaction #360909
product
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
c1cc2c(cc1C1CO1)OCO2
Reaction #361268
3,4-methylenedioxyphenyloxirane
Ausbeute 91.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(O)(c2ccc3c(c2)OCO3)CC1
Reaction #362075
product
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Oc1c(Cl)cc(Cn2c(=O)n(C(=O)OCC)c3ccccc32)cc1Cl)c1ccc2c(c1)OCO2
Reaction #362118
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Oc1ccc(CBr)cc1)c1ccc2c(c1)OCO2
Reaction #362126
title compound
Ausbeute 109.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Oc1ccc(Cn2c(=O)n(C(=O)OCC)c3ccccc32)cc1)c1ccc2c(c1)OCO2
Reaction #362127
title compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
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