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116099

COC(=O)c1cc(-c2ccc(OCc3ccccc3)cc2OC)cc(C(=O)OC)n1
Reaction #5646
diester
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(-c2ccc(O)cc2OC)cc(C(=O)OC)n1
Reaction #5647
phenol
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cc(C(=O)O)nc(C(=O)O)c2)c(OC)c1
Reaction #5649
SiO2
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)nc(C(=O)O)c1
Reaction #67916
4,6-dimethyl-2-pyridinecarboxylic acid
Выход 122.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(-c2ccnc(Cl)c2)cc(C)n1
Reaction #178323
DOI: 10.1039/C8SC04228D
Cc1cc(-c2cc(F)cc(F)c2)cc(C(=O)Nc2ncc(F)s2)n1
Reaction #183183
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc(-c2c(OC)cc(OC)cc2OC)cc(C(=O)OCC)n1
Reaction #199895
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc(-c2cncnc2)cc(C)n1
Reaction #229599
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(C)nc(C(=O)O)c1
Reaction #247069
DOI: 10.1039/C8SC04228D
Cc1cc(-c2cc(F)cc(F)c2)cc(C(=O)Nc2ccnc(C#N)c2)n1
Reaction #253723
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc(C)cc(-c2ccc(NC(=O)OCc3ccccc3)cc2)n1
Reaction #259917
DOI: 10.1039/C8SC04228D
Cc1ccc(NC(=O)c2cc(-c3cc(F)cc(F)c3)cc(C)n2)nc1
Reaction #276311
DOI: 10.1039/C8SC04228D
CC(=O)c1c(-c2cccc([N+](=O)[O-])c2)cc(C(=O)NCCN2CCOCC2)nc1C
Reaction #278867
DOI: 10.1039/C8SC04228D
Cc1cc(-c2ccnc(Cl)c2)cc(C(=O)Nc2ccc(Cl)cn2)n1
Reaction #284187
DOI: 10.1039/C8SC04228D
COCc1csc(NC(=O)c2cc(-c3cc(F)cc(F)c3)cc(C)n2)n1
Reaction #284880
DOI: 10.1039/C8SC04228D
Cc1cc(-c2cncc(F)c2)cc(C(=O)Nc2ccc(Cl)cn2)n1
Reaction #285113
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(C(=O)O)cc(C)n1
Reaction #287348
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc(-c2c(OC)cc(OC)cc2OC)cc(CO)n1
Reaction #292970
DOI: 10.1039/C8SC04228D
CCCCc1cc(C(=O)Nc2nnn[nH]2)nc(-c2ccc([N+](=O)[O-])cc2)c1
Reaction #299484
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(C(=O)OC)c2c(n1)C(=O)C1(OCCO1)c1cc(C(=O)OC)[nH]c1-2
Reaction #305083
Trimethyl 5′-oxo-1′,5′-dihydrospiro[[1,3]dioxolane-2,4′-pyrrolo[2,3-f]quinoline]-2′,7′,9′-tricarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
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