Recherche de Sous-structure

1306848

COC(=O)c1cc(-c2ccc(OCc3ccccc3)cc2OC)cc(C(=O)OC)n1
Reaction #5646
diester
Rendement 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(-c2ccc(O)cc2OC)cc(C(=O)OC)n1
Reaction #5647
phenol
Rendement 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
O=C(OCCl)OCc1cccc(COC(=O)OCCl)n1
Reaction #63261
2,6-bis(chloromethyloxy-carbonyloxymethyl)pyridine
Rendement 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)O.CNC(=O)O.OCc1cccc(CO)n1
Reaction #63262
title compound
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2cccc(CO)n2)OCCO1
Reaction #71062
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2cccc(COS(C)(=O)=O)n2)OCCO1
Reaction #71063
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2cccc(Cn3ncc([N+](=O)[O-])n3)n2)OCCO1
Reaction #71064
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(OCCCC(C)(C)SSC)cc(C(=O)OCC)n1
Reaction #86283
diethyl 4-(4-methyl-4-(methyldisulfanyl)pentyloxy)pyridine-2,6-dicarboxylate
Rendement 52.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(COS(C)(=O)=O)n1
Reaction #185866
DOI: 10.1039/C8SC04228D
COC(=O)c1cccc(CNCc2ccc(F)cc2)n1
Reaction #198489
DOI: 10.1039/C8SC04228D
COC(=O)CCOCCOCCOCCOCCNC(=O)CSC(C)(C)CN(C)CCOc1cc(CO)nc(CO)c1
Reaction #199887
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc(-c2c(OC)cc(OC)cc2OC)cc(C(=O)OCC)n1
Reaction #199895
DOI: 10.1039/C8SC04228D
COC(=O)c1cccc(COc2ccc(-c3cc4c(ncn4C)c(C#N)n3)cc2C(F)(F)F)n1
Reaction #210451
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc(OC)cc(C(=O)OCC)n1
Reaction #213761
DOI: 10.1039/C8SC04228D
BrCc1cccc(COC(c2ccccc2)(c2ccccc2)c2ccccc2)n1
Reaction #231961
DOI: 10.1039/C8SC04228D
CC1(c2cccc(Cn3cc([N+](=O)[O-])cn3)n2)OCCO1
Reaction #232574
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(Br)cc(C(=O)O)n1
Reaction #234024
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cccc(CO)n1
Reaction #234128
DOI: 10.1039/C8SC04228D
O=S(=O)(Nc1ncc(Cl)nc1OCc1cccc(CO)n1)c1cccc(Cl)c1Cl
Reaction #250264
DOI: 10.1039/C8SC04228D
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