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pro vyhledávání: '"Gerard P. Moss"'
Autor:
Michel Vert, Jiazhong Chen, Andrey Yerin, Karl-Heinz Hellwich, Roger C. Hiorns, Richard Jones, Graeme Moad, Gerard P. Moss
Publikováno v:
Pure and Applied Chemistry. 94:559-571
A number of human activities require that certain complex molecules, referred to as active species (drugs, dyes, peptides, proteins, genes, radioactive labels, etc.), be combined with substrates, often a macromolecule, to form temporary or permanent
Publikováno v:
Pure and Applied Chemistry. 93:243-252
According to the 1994 IUBMB-IUPAC Joint Commission on Biochemical Nomenclature (JCBN) on chemical and biochemical reactions, two categories of thermodynamics, based on different concepts and different formalisms, are established: (i) chemical thermod
Autor:
Amélia P. Rauter, Marcus Ennis, Ida Schomburg, Bernardo J. Herold, Gerard P. Moss, Derek Horton, Karl-Heinz Hellwich
Publikováno v:
Pure and Applied Chemistry. 90:1429-1486
Flavonoid structures, found in nature or obtained by synthesis, may be very complex. These Recommendations provide a guide for flavonoid aglycone names. This will also allow the construction of the names for their polyglycosylated species with clarit
Autor:
Ulf Göransson, Pramodkumar D. Jadhav, Jianheng Shen, Ning-Hua Tan, Gerard P. Moss, Youn Young Shim, Martin J. T. Reaney, David J. Craik
Publikováno v:
Peptide Science. 106:917-924
In 2015, an International Union of Pure and Applied Chemistry (IUPAC) Task Group was formed to develop nomenclature recommendations for homodetic cyclic peptides produced from ribosomal precursors. Delegates of the 2015 International Conference on Ci
Autor:
Gerard P. Moss, Jonathan P. Waltho, G. Michael Blackburn, Nigel G. J. Richards, Jacqueline Cherfils, Nicholas H. Williams, Alfred Wittinghofer
Publikováno v:
Blackburn, G M, Cherfils, J, Moss, G P, Richards, N G J, Waltho, J P, Williams, N H & Wittinghofer, A 2017, ' How to name atoms in phosphates, polyphosphates, their derivatives and mimics, and transition state analogues for enzyme-catalysed phosphoryl transfer reactions (IUPAC Recommendations 2016) ', Pure and Applied Chemistry, vol. 89, no. 5, pp. 653-675 . https://doi.org/10.1515/pac-2016-0202
Procedures are proposed for the naming of individual atoms, P, O, F, N, and S in phosphate esters, amidates, thiophosphates, polyphosphates, their mimics, and analogues of transition states for enzyme-catalyzed phosphoryl transfer reactions. Their pu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c420608b2654f5bc3e0d6f862e80b96
Autor:
Gerard P. Moss, Henri A. Favre, A. D. McNaught, Karl-Heinz Hellwich, Warren H. Powell, P. M. Giles
Publikováno v:
Pure and Applied Chemistry. 76:1283-1292
Since publication of "Revised Section F: Natural products and related compounds" in Pure Appl.Chem. 71, 587-643 (1999), a number of errors have been detected. Further consideration of some sections now requires some extensions or further explanation.
Publikováno v:
Pure and Applied Chemistry. 74:629-695
Fullerenes are a new allotrope of carbon characterized by a closed-cage structure consisting of an even number of three-coordinate carbon atoms devoid of hydrogen atoms. This class was originally limited to closed-cage structures with 12 isolated fiv
Autor:
Gerard P. Moss
Publikováno v:
Pure and Applied Chemistry. 72:1493-1523
Lignans and neolignans are a large group of natural products characterized by the coupling of two C6C3 units. For nomenclature purposes the C6C3 unit is treated as propylbenzene and numbered from 1 to 6 in the ring, starting from the propyl group, an
Publikováno v:
Pure and Applied Chemistry. 71:1327-1330
Among the names and structures used as examples in the 1993 Guide to IUPAC Nomenclature of Organic Compounds some errors appear, several of which are likely to be quickly obvious and untroublesome. To reduce the possibility of confusion among users o
Publikováno v:
Tetrahedron Letters. 37:2877-2880
3,8-Dioxatricyclo[3.2.1.0 2,4 ]octane derivatives are readily prepared by the Diels Alder reaction of furan followed by epoxidation. The oxygen atoms are cis to each other and when treated with Lewis acids such as BF 3 rearrange stereospecifically to