bromotrimethylsilane

CCCCCC(N)CC(P(=O)([O-])[O-])P(=O)([O-])O.[NH4+].[NH4+].[NH4+]
Reaction #2073
3-aminooctane-1,1-bisphosphonic acid, triammonium salt
Ausbeute 419.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOCn1cnc2c1c(=O)n(CCCCP(=O)([O-])[O-])c(=O)n2C.[NH4+].[NH4+]
Reaction #2117
Diammonium [4-(7-ethoxymethyl-3-methylxanthin-1-yl)butyl]phosphonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=P(O)(O)C(Cn1ccnc1)S(=O)(=O)O
Reaction #2787
2-(1-imidazolyl)-1-phosphonoethanesulfonic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1ncnc2c1ncn2OCCOCP(=O)(O)O
Reaction #6356
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Nc1nc(Cl)c2ncn(OCCOCP(=O)(O)O)c2n1
Reaction #6359
title compound
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Nc1ncnc2c1ncn2OC[C@@H](CO)OCP(=O)(O)O
Reaction #6364
(R)-9-[3-Hydroxy-2-(phosphonomethoxy)propoxy]adenine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Nc1nc2c(ncn2OC[C@H](CO)OCP(=O)(O)O)c(=O)[nH]1
Reaction #6367
title compound
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Nc1ncnc2c1ncn2OC[C@H](CO)OCP(=O)(O)O
Reaction #6370
title compound
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
—
Reaction #6434
5.001
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
c1ncc2cn[nH]c2n1
Reaction #53248
pyrazolo[3,4-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1c(C)c2c(c(O)c1CC=C(C)C=CP(=O)(O)O)C(=O)OC2
Reaction #61226
[5-(4-Hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dihydro-isobenzofuran-5-yl)-3-methyl-penta-1,3-dienyl]-phosphonic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1c(C)c2c(c(O)c1CCOCP(=O)(O)O)C(=O)OC2
Reaction #61249
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1c(C)c2c(c(O)c1CC=C(C)CP(=O)(O)O)C(=O)OC2
Reaction #61252
product
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1c(C)c2c(c(O)c1CC=C(C)CNCCP(=O)(O)O)C(=O)OC2
Reaction #61255
product
Ausbeute 36.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1c(C)c2c(c(O)c1CC=C(C)CN(CCP(=O)(O)O)S(C)(=O)=O)C(=O)OC2
Reaction #61257
desired product
Ausbeute 73.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1c(C)c2c(c(O)c1CC=C(C)CN(CCP(=O)(O)O)C(C)=O)C(=O)OC2
Reaction #61259
product
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1c(C)c2c(c(O)c1CC=C(C)CN(CCP(=O)(O)O)Cc1ccccc1)C(=O)OC2
Reaction #61261
product
Ausbeute 96.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1c(C)c2c(c(O)c1CC=C(C)CN(C=O)CCP(=O)(O)O)C(=O)OC2
Reaction #61263
product
Ausbeute 50.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1c(C)c2c(c(O)c1CC=C(C)CNCP(=O)(O)O)C(=O)OC2
Reaction #61264
product
Ausbeute 39.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1c(C)c2c(c(O)c1CC=C(C)CC(C#N)P(=O)(O)O)C(=O)OC2
Reaction #61267
desired product
Ausbeute 60.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
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