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NC1(c2ccc(-c3c(-c4ccccc4)oc4c(C(=O)O)cccc4c3=O)cc2)CCC1
Reaction #181932
DOI: 10.1039/C8SC04228D
Cc1c(-c2ccccc2)oc2c(C(=O)NCC(C)N3CCCCC3)cccc2c1=O
Reaction #192414
DOI: 10.1039/C8SC04228D
Cc1c(-c2ccccc2)oc2c(C(=O)O)cccc2c1=O
Reaction #205211
DOI: 10.1039/C8SC04228D
CCN(CC)CCNC(=O)c1cccc2c(=O)c(C)c(-c3cccc(Cl)c3)oc12
Reaction #231129
DOI: 10.1039/C8SC04228D
COC(=O)c1cccc2c(=O)c(C)c(-c3ccccc3)oc12
Reaction #291803
DOI: 10.1039/C8SC04228D
Cc1c(-c2ccccc2)oc2c(C(=O)OCC3CO3)cccc2c1=O
Reaction #552163
2,3-epoxypropyl 3-methylflavone-8-carboxylate
Ausbeute 75.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(-c2oc3c(C(=O)NCCCN4CCCCC4)cccc3c(=O)c2C)c1
Reaction #906929
DOI: 10.1039/C8SC04228D
Cc1c(-c2ccccc2)oc2c(C(=O)OCCCBr)cccc2c1=O
Reaction #916713
DOI: 10.1039/C8SC04228D
Cc1c(-c2ccccc2)oc2c(C(=O)O)cccc2c1=O
Reaction #1044072
DOI: 10.1039/C8SC04228D
Cc1c(-c2ccccc2)oc2c(C(=O)O)cc(Cl)cc2c1=O
Reaction #1067167
white powder
Ausbeute 90.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)cc2c(=O)c(C)c(-c3ccccc3)oc12
Reaction #1067168
white crystal
Ausbeute 90.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(Cl)cc2c(=O)c(C)c(-c3ccccc3)oc12
Reaction #1067169
white crystals
Ausbeute 89.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)oc2c(C(=O)OCCN3CCCCC3)cc(Cl)cc2c1=O
Reaction #1067170
white crystals
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)oc2c(C(=O)OCCN3CCOCC3)cc(Cl)cc2c1=O
Reaction #1067171
morpholinoethyl 6-chloro-3-methylflavone-8-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc2c(=O)c(C)c(-c3ccccc3)oc12
Reaction #1067172
white needle-like
Ausbeute 82.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)oc2c(C(=O)O)cccc2c1=O
Reaction #1067173
3-methylflavone-8-carboxylic acid
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)oc2c(C(=O)O)cccc2c1=O
Reaction #1067174
3-methylflavone-8-carboxylic acid
Ausbeute 97.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc2c(=O)c(-c3ccc(C4(NC(=O)OC(C)(C)C)CCC4)cc3)c(-c3ccccc3)oc12
Reaction #1124587
title compound
Ausbeute 200.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1(c2ccc(-c3c(-c4ccccc4)oc4c(C(=O)O)cccc4c3=O)cc2)CCC1
Reaction #1124588
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1(c2ccc(-c3c(-c4ccccc4)oc4c(C(=O)O)cccc4c3=O)cc2)CCC1
Reaction #1124589
title compound
Ausbeute 69.4%DOI: 10.6084/m9.figshare.5104873.v1
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