Organic compounds -- part of the class 532-570 series – Organic compounds – Phosphorus esters
Patent
1993-09-09
1995-05-30
Lee, Mary C.
Organic compounds -- part of the class 532-570 series
Organic compounds
Phosphorus esters
C07F 909
Patent
active
054203287
ABSTRACT:
Phsophonate esters can be synthesized in high yields by condensations of alcohols with methyl phosphonates followed by selective demethylation. The reaction is general, relativly insensitive to steric constraints of hindered phosphonic acids, and can also be carried out on a solid support to synthesize large collections of compounds to screen for pharmacological activity.
REFERENCES:
patent: 5143854 (1992-09-01), Pirrung et al.
patent: 5183810 (1993-02-01), Greenlee et al
Gilmore et al., 1974, J. Pharm. Sci. 63: 965-966 New compounds: Monoesters of a-Aminobenzylphosphonic Acid.
Loibner and Zbiral, 1976, Helvetica Chimica Acta 59 (6): 2100-2113 Reaktionen mit phosphororganischen Verbindungen.XLI[1]') Neuartige synthetische Aspekte des systems Triphenylphoshin-Azodicarbonsaureester-Hydroxyverbindung.
Kurihara et al., 1976, Tetrahedron Ltrs. 28: 2455-2458 Synthesis of lactones and cycloalkanes. Cyclization of w-hydroxy acids and ethyl a-cyano-w-hydroxycarboxylates.
Wasielewski et al., 1976, J. Rocz. Chem. 50: 1613-1620 Aminophosphonic acids, part VIII. application of trichloroacetonitrile for preparation of a-aminophosphonic acid monoesters.
Balthazor and Flores, 1980, J. Org. Chem. 45: 529-531 Dipolar Cycloadditions of an Acetylenic phosphinate.
Mitsunobu, 1981, Synthesis pp. 1-28 The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products.
Vargas et al., 1984, Biochim. Biophys. Acta 796: 123-128 Inhibition of Platelet phosphatidylinositol synthetase by an analog of CDP-Diacylglycerol.
Karanewsky and Badia, 1986, Tetrahedron Ltrs. 27 (16): 1751-1754 Synthesis of phosphonic monoesters from phosphonous.
Hoffmann, Jul. 1986, Communications: Synthesis, pp. 557-559 A convenient synthesis of alkyl Hydrogen 1-(Benzyloxycarbonylamino)-alkanephosphonates.
Pollack et al., 19 Dec. 1986, Science 234: 1570-1573 Selective Chemical Catalysis by an Antibody.
Tramontano et al., 19 Dec. 1986, Science 234: 1566-1570 Catalytic Antibodies.
Blackburn et al., 1987, Nucl. Acids Res. 15: 6991-7004 Synthesis and resistance to enzymic hydrolysis of stereochemically-defined phosphonate and thiophosphate analogues of P1,P4-bis (5'-adenosyl)-tetraphosphate.
Norbeck et al., 1987, J. Org. Chem. 52: 2174-2179 Synthesis of an Isoteric Phosphonate Analogue of Cytidine 5'-Monophospho--3-deoxy-D-manno-2-octulosonic Acid.
Jacobs et al., 1 Apr. 1987, J. Amer. Chem. Soc. 109: 2174-2176 Catalytic Antibodies.
Biller et al., Oct. 1988, J. Medicinal Chemistry 31 (10): 1869-1871 Isoprenoid (Phosphinylmethyl) phosphonates as inhibitors of squalene synthetase.
Bartlett et al., 1990, J. Org. Chem. 55 (26): 6268-6274 Potent Inhibitions of Pepsin and Penicillopepsin by Phosphorus-Containing Peptide Analogues.
Kaplan et al., 1991, Biochemistry 30 (33): 8165-8170 Synthesis and Evaluation of an Inhibitor of Carboxypeptidase A with a Ki Value in the Femtomolar Range.
Morgan et al., 1991, J. Am. Chem. Soc. 113 (1): 297-307 Differential binding energy: a detailed evaluation of the influence of hydrogen-bonding and hydrophobic groups on the inhibition of thermolysin by phosphorus-containing inhibitors.
Kimura et al., 1979, Bull. Chem. Soc. Japan 52(4): 1191-1196 Studies on nucleosides and nucleotides. VII. Preparation of pyrimidine nucleoside 5'-Phosphonates and.
Affymax Technologies N.V.
Ambrose Michael G.
Kaster Kevin
Lee Mary C.
Norviel Vern
LandOfFree
Methods for the synthesis of phosphonate esters does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Methods for the synthesis of phosphonate esters, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Methods for the synthesis of phosphonate esters will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-363566