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24662

CCCCC1=C(Br)c2cc3c(cc2C1)OCO3
Reaction #62987
2-n-butyl-3-bromo-5,6-methylenedioxyindene
Ausbeute 68.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1=C(N(CC)CC)c2cc3c(cc2C1)OCO3
Reaction #62991
2-n-butyl-3-diethylamino-5,6-methylenedioxyindene
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Br)c1cc2c(cc1Cl)OCO2
Reaction #192298
DOI: 10.1039/C8SC04228D
CC(C)CCOCCCCCCOCCCCCCOCc1ccc2c(c1)OCO2
Reaction #208679
DOI: 10.1039/C8SC04228D
Clc1cc2c(cc1CBr)OCO2
Reaction #220366
powder
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)N(C2C3CC4CC(C3)CC2C4)N1Cc1ccc2c(c1)OCO2
Reaction #229973
DOI: 10.1039/C8SC04228D
O=C(O)C(Br)c1ccc2c(c1)OCO2
Reaction #276996
DOI: 10.1039/C8SC04228D
CCOC(=O)c1ccc(Cc2ccc3c(c2)OCO3)o1
Reaction #349391
Ethyl 5-(3,4-methylenedioxybenzyl)-2-furoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Br)c1ccc2c(c1)OCO2
Reaction #362109
methyl 2-bromo-2-(3,4-methylenedioxyphenyl)acetate
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(CO)cc(Cl)c1OC(C(=O)OC)c1ccc2c(c1)OCO2
Reaction #362114
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(Cn2c(=O)n(C(=O)OCC)c3ccccc32)ccc1OC(C(=O)OCC)c1ccc2c(c1)OCO2
Reaction #362123
title compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(c1ccc2c(c1)OCO2)c1cn(C)c2cc(CO)ccc12
Reaction #388262
DOI: 10.1039/C8SC04228D
Cn1cc(C(C(=O)O)c2ccc3c(c2)OCO3)c2ccc(C(=O)OCc3ccccc3)cc21
Reaction #409269
subtitle compound
Ausbeute 60.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(Br)c1ccc2c(c1)OCO2
Reaction #409275
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(C(C(=O)O)c2ccc3c(c2)OCO3)c2cc(Br)ccc21
Reaction #456522
subtitle compound
Ausbeute 79.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Br)c1ccc2c(c1)OCO2
Reaction #468503
Methyl 2-(1,3-benzodioxol-5-yl)-2-bromoacetate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(c1ccc2c(c1)OCO2)c1cn(C)c2cc(CO)ccc12
Reaction #468504
subtitle compound
Ausbeute 77.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(c1ccc2c(c1)OCO2)c1cn(C)c2ccc(Br)cc12
Reaction #468508
subtitle compound
Ausbeute 76.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(c1cc(OC)c2c(c1)OCO2)c1c[nH]c2cc(Br)ccc12
Reaction #468511
subtitle compound
Ausbeute 88.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Br)c1cc2c(cc1Cl)OCO2
Reaction #468513
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
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