Zobrazeno 1 - 10
of 95
pro vyhledávání: '"Thomas D. Inch"'
Publikováno v:
Pure and Applied Chemistry. 74:2323-2352
This document was prepared as a report from IUPAC to the Organisation for the Prohibition of Chemical Weapons (OPCW) to provide an evaluation of scientific and technological advances in the chemical sciences relevant to the Chemical Weapons Conventio
Autor:
Thomas D. Inch
Publikováno v:
Ciba Foundation Symposium 57-Phosphorus in the Enviroment: Its Chemistry and Biochemistry
Organophosphorus anticholinesterase compounds may be derivatives of phosphoric acid or of a phosphonic acid. The phosphonic acid derivatives are usually more reactive and more toxic than the phosphoric acid derivatives. Examples are given to show tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::540c4dd0e25b4cc46b74d8354258962c
https://doi.org/10.1002/9780470720387.ch8
https://doi.org/10.1002/9780470720387.ch8
Publikováno v:
Biochemical Journal. 155:1-4
6,7 -Dideoxy-α-D-gluco-heptose 7-phosphonic acid, the isosteric phosphonate analogue of glucose 6-phosphate, was synthesized in six steps from the readily available precursor benzyl 4,6-O-benzylidene-α-D-glucopyranoside. The analogue is a substrate
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :639-643
1,3,2-Oxazaphospholidine-2-thiones derived from (+)-norephedrine react with alkoxide to give a product of kinetic control, formed by endocyclic P–O cleavage with inversion of configuration, and one of thermodynamic control, formed by endocyclic P
Publikováno v:
Tetrahedron Letters. 20:5051-5054
Tetra-O-benzyl-α-D-glucopyranosyl bromide in dichloromethane reacts stereospecifically with solutions of phenols in aqueous sodium or potassium hydroxide, in the presence of phase transfer catalysts, to give good yields of tetra-O-benzyl aryl-β-D-g
Publikováno v:
Phosphorus and Sulfur and the Related Elements. 10:229-232
Added lithium cation has no effect on the stereochemical outcome of the displacement of chloride or p-nitrophenoxide from phosphorus in acyclic and some cyclic molecules. In other cyclic systems th...
Publikováno v:
Tetrahedron. 41:4909-4917
With R-(+) ethyl (or methyl) S-methyl methylphosphonothioate and (+)-pinacolyl alkoxide competitive and highly stereoselective displacements of O-alkyl and S-methyl occur, both reactions being with inversion of configuration. With the enantiomeric S-
Autor:
C. Richard Hall, Thomas D. Inch
Publikováno v:
Tetrahedron. 36:2059-2095
The stereochemistry of endocyclic and exocyclic bond forming and breaking processes in 5- and 6-membered cyclic phosphorus esters is summarised and comparisons are made with analogous reactions in acyclic phosphorus esters. The factors that determine
Publikováno v:
Tetrahedron Letters. 20:3557-3560
The reaction provides a new phosphonylation procedure for simple alcohols. Results obtained in inert solvents are consistent with the intermediacy of a phosphorus hemiacetal.
Autor:
D. G. Upshall, M. C. French, David J. Sellers, C. R. Hall, Thomas D. Inch, Andrew P. Smith, J. M. Harrison, P. Watts
Publikováno v:
Pesticide Biochemistry and Physiology. 24:53-60
R (+)-Ethyl S -propyl methylphosphonothioate is bioactivated both in vivo and when perfused through isolated liver to give a product which is much more active as an inhibitor of acetylcholinesterase than the parent compound. The bioactivation does no