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335869

CCCCC(C(=O)OCC)C(=O)C(=O)OCC
Reaction #486169
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(C(=O)C(=O)OCC)C(=O)c1ccccc1
Reaction #544539
product ( 172 )
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(C(=O)OCC)C(=O)C(=O)OCC
Reaction #699617
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(C(=O)OCC)=C(Nc1ccccc1)C(=O)OCC
Reaction #754702
DOI: 10.1039/C8SC04228D
CCCCC(C(=O)OCC)=C(Nc1ccccc1)C(=O)OCC
Reaction #1197294
expected product
Ausbeute 45.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)N(CCc2c[nH]c3ccccc23)CCC1
Reaction #1208661
DOI: 10.1039/C8SC04228D
CCOC(=O)c1nn(-c2cccnc2)c(-c2ccccc2)c1C
Reaction #1524394
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C(F)C(=O)c1ccccc1
Reaction #1524396
3-Fluoro-4-phenyl-2,4-dioxobutanoic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1c(-c2ccccc2)nn(-c2ccccn2)c1O
Reaction #1555140
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(C(=O)OCC)=C(Nc1ccccc1)C(=O)OCC
Reaction #1690114
expected product
Ausbeute 45.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(C(=O)OCC)=C(Nc1ccc(C(=O)OC)cc1)C(=O)OCC
Reaction #1690128
expected product
Ausbeute 100.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(C(=O)C(=O)OCC)C(=O)c1ccccc1
Reaction #1730373
product ( 172 )
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)N(CCc2c[nH]c3ccccc23)CCC1
Reaction #1992597
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1c(-c2ccccc2)nn(-c2ccccn2)c1O
Reaction #1999126
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(C(=O)OCC)=C(Nc1ccccc1)C(=O)OCC
Reaction #2347996
expected product
Ausbeute 45.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C(F)C(=O)c1ccccc1
Reaction #2411559
DOI: 10.1039/C8SC04228D
CCCCC(C(=O)C(=O)OCC)C(=O)c1ccccc1
Reaction #2431063
DOI: 10.1039/C8SC04228D