trimethyl phosphite

CCOC(=O)c1ccc(CP(=O)(OC)OC)c(C(F)(F)F)c1
Reaction #42035
objective compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)C(CC=CCP(=O)(OC)OC)CC(C)=CCc1c(O)c2c(c(C)c1OC)COC2=O
Reaction #61234
product
Yield 88.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1c(C)c2c(c(O)c1CC=C(C)CP(=O)(OC)OC)C(=O)OC2
Reaction #61251
desired product
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCC(=CCc1c(O)c2c(c(C)c1OC)COC2=O)CP(=O)(O)O
Reaction #61273
product
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COC(=O)C(CC=CCP(=O)(OC)OC)CC(C)=CCc1c(O)c2c(c(C)c1OC)COC2=O
Reaction #61898
product
Yield 88.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1c(C)c2c(c(O)c1CC=C(C)CP(=O)(OC)OC)C(=O)OC2
Reaction #61915
desired product
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCC(=CCc1c(O)c2c(c(C)c1OC)COC2=O)CP(=O)(O)O
Reaction #61934
product
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCC(=CCc1c(O)c2c(c(C)c1CC)COC2=O)CP(=O)(O)O
Reaction #61951
product
Yield 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COP(=O)(CCC(CCP(=O)(OC)OC)c1c2nc(cc3ccc([nH]3)c(-c3ccc(OCC(=O)OC(C)(C)C)cc3)c3nc(cc4ccc1[nH]4)C=C3)C=C2)OC
Reaction #68814
solid
Yield 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cc(CP(=O)(OC)OC)cc(C)c1O
Reaction #77201
dimethyl (4-hydroxy-3-methoxy-5-methylbenzyl)phosphonate
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COC(=O)c1ccn2c(F)c(-c3ccccc3)nc2c1
Reaction #88407
title compound
Yield 86.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C=C1C[C@@H]2[C@H](CC[C@@]3(C)[C@H]2CC(=C)[C@]3(O)C(C)=O)[C@@]2(C)CCC(=O)C=C12
Reaction #93686
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
C=C(CP(=O)(OC)OC)CP(=O)(OC)OC
Reaction #95547
title compound
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
COP(=O)(Cc1ccc(-c2nc3ccccc3s2)nc1)OC
Reaction #175655
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COP(=O)(Cc1ccc([N+](=O)[O-])s1)OC
Reaction #182039
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(CC=CCP(=O)(OC)OC)CC(C)=CCc1c(O)c2c(c(C)c1OC)COC2=O
Reaction #187219
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COP(=O)(Cc1ccc2ccccc2c1)OC
Reaction #190540
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCCCCCCCCCP(=O)(OC)OC
Reaction #191487
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COP1OC(C)CC(C)O1
Reaction #194625
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COP(=O)(OC)C(=O)OC1CCCCC1
Reaction #237867
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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