Zobrazeno 1 - 10
of 465
pro vyhledávání: '"Derek Horton"'
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:
Derek Horton
Publikováno v:
Carbohydrate Research. 403:3-7
The article traces the history of the journal Carbohydrate Research from its debut in 1964 and its subsequent evolution to the present day, viewed from the perspective of one of the founding editors who served as a receiving editor until 2005. The co
Autor:
David C. Baker, Derek Horton
Advances in Carbohydrate Chemistry and Biochemistry, part of a long running serial that began in 1945, provides critical and informative articles written by research specialists that integrate the industrial, analytical, and technological aspects of
Autor:
Derek Horton, John H. Lauterbach
Publikováno v:
The Journal of Organic Chemistry. 83:1686-1686
Autor:
Scott M. Vejcik, Derek Horton
Publikováno v:
Carbohydrate Research. 342:806-818
Acetylated d -pentose diethyl dithioacetals were coupled by way of 1-bromo-1-ethylthio derivatives with 2,4-bis(trimethylsilyl)thymine to afford diastereomeric pairs of acyclic-sugar nucleoside analogues bearing a thymin-1-yl and an ethylthio group a
Autor:
Derek Horton, Michael S. Alexander
Publikováno v:
Carbohydrate Research. 342:31-43
1,6-Anhydro-4-deoxy-4-diazo-2,3-O-isopropylidene-β- d -lyxo-hexopyranose (4) is a stable crystalline compound readily accessible by an improved synthetic procedure. It has been used as a model for evaluating the reactivity of the diazo group, when n
Autor:
Anakshi Khare, Derek Horton
Publikováno v:
Carbohydrate Research. 341:2631-2640
The methyl beta-glycoside of the title sugar, obtained from 2-deoxy-2-fluoro-beta-D-glucopyranose tetraacetate by a sequence with detailed characterization of all intermediates, was converted by acetolysis-bromination into 3,4-di-O-acetyl-2,6-dideoxy
Autor:
Derek Horton
Since its inception in 1945, this serial has provided critical and informative articles written by research specialists that integrate industrial, analytical, and technological aspects of biochemistry, organic chemistry, and instrumentation methodolo
Publikováno v:
Carbohydrate Research. 334:195-205
Based on a literature precedent, preparation of methyl 4-azido-3,4,6-trideoxy-3-fluoro-alpha-D-mannopyranoside (18) was attempted via fluorination of methyl 4-azido-2-O-benzyl-4,6-dideoxy-alpha-D-altropyranoside with diethylaminosulfur trifluoride (D