Tetraethyl methylenebisphosphonate

CCCCNC(=O)CC(P(=O)(OCC)OCC)P(=O)(OCC)OCC
Reaction #2068
title compound
المردود 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOP(=O)(C=Cc1nc(-c2ccccc2)oc1COc1ccc(OCc2nc(-c3ccccc3)oc2C)cc1)OCC
Reaction #187298
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOP(=O)(C=Cc1cn(CCO)nc1OCc1ccc(OCc2nc(-c3ccco3)oc2C)c(OC)c1)OCC
Reaction #211145
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOP(=O)(C=Cc1cn(-c2ccccc2)nc1N(C)Cc1ccc(OCc2nc(-c3ccco3)oc2C)c(OC)c1)OCC
Reaction #223019
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOP(=O)(C=Cc1cn(-c2ccccc2)nc1OCc1ccc(OCc2nc(-c3ccco3)oc2C)c(OC)c1)OCC
Reaction #227374
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)c1ccc(-c2nc(COc3ccc(COc4nn(-c5ccccc5)cc4C=CP(=O)(OCC)OCC)cc3OC)c(C)o2)o1
Reaction #228155
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOP(=O)(C=Cc1cn(-c2ccccc2)nc1OCc1ccc(OCc2nc(-c3cccnc3)oc2C)c(OC)c1)OCC
Reaction #235909
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOP(=O)(OCC)C(Cc1cnsn1)P(=O)(OCC)OCC
Reaction #239277
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)c1cn2c(C=CP(=O)(OCC)OCC)cccc2n1
Reaction #246167
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOP(=O)(C=Cc1cn(-c2ccccc2)nc1OCc1ccc(OCc2nc(-c3ccccc3C(=O)OC)oc2C)c(OC)c1)OCC
Reaction #246512
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOP(=O)(C=Cc1cc(-n2c(=O)cc(C(F)(F)F)n(C)c2=O)ccc1Cl)OCC
Reaction #266771
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOP(=O)(C=Cc1cn(-c2ccccc2)nc1OCc1ccc(OCc2nc(-c3ccccc3)oc2C)c(OC)c1)OCC
Reaction #269809
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOP(=O)(C=Cc1cn(CC)nc1OCc1ccc(OCc2nc(-c3ccco3)oc2C)c(OC)c1)OCC
Reaction #277507
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOP(=O)(C=Cc1cn(-c2ccccc2)nc1OCc1ccc(OCc2cn(-c3ccccn3)nc2C)c(OC)c1)OCC
Reaction #282760
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOP(=O)(OCC)C(Cc1nccn1Cc1ccccc1)P(=O)(OCC)OCC
Reaction #284212
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOP(=O)(C=Cc1cnc(-c2ccccc2)nc1OCc1ccc(OCc2nc(-c3ccco3)oc2C)c(OC)c1)OCC
Reaction #293916
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)C1CCN(c2nc(COc3ccc(COc4nn(-c5ccccc5)cc4C=CP(=O)(OCC)OCC)cc3OC)c(C)s2)CC1
Reaction #299447
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCCCc1ccc(C2CCC(C=CP(=O)(OCC)OCC)(NC(=O)OC(C)(C)C)C2)cc1
Reaction #379338
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOP(=O)(OCC)C(C(=CC(=O)OC)C(=O)OC)P(=O)(OCC)OCC
Reaction #379809
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)C1C(CP(=O)(OCC)OCC)=CCN1C(=O)OCC
Reaction #432513
ethyl 1-ethoxycarbonyl-3-(diethylphosphonomethyl)-2,5-dihydropyrrole-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_10
الصفحة 1التالي