Zobrazeno 1 - 10
of 53
pro vyhledávání: '"J. W. McFarland"'
Publikováno v:
Ecosphere, Vol 10, Iss 8, Pp n/a-n/a (2019)
Abstract Along the coastal fringe of the Yukon–Kuskokwim River Delta in southwestern Alaska, geese maintain grazing lawns dominated by a rhizomatous sedge that, when ungrazed, transitions to a taller, less palatable growth form that is taxonomicall
Externí odkaz:
https://doaj.org/article/3e7c78e0bbb14d35ace75e4859ff678a
Autor:
C. W. HEDBERG, F. J. ANGULO, K. E. WHITE, C. W. LANGKOP, W. L. SCHELL, M. G. STOBIERSKI, A. SCHUCHAT, J. M. BESSER, S. DIETRICH, L. HELSEL, P. M. GRIFFIN, J. W. McFARLAND, M. T. OSTERHOLM, null THE INVESTIGATION TEAM
Publikováno v:
Epidemiology and Infection. 122:385-393
Laboratory-based surveillance of salmonella isolates serotyped at four state health departments (Illinois, Michigan, Minnesota and Wisconsin) led to the identification of multistate outbreaks of salmonella infections during 1990 (176 cases of S. javi
Publikováno v:
Journal of Heterocyclic Chemistry. 32:1747-1750
Formylation of 2,2′,5′,2′-terfuran (1) with N-methylformanilide and phosphorus oxychloride gave 5-formyl-2,2′,5′,2′-terfuran (2) and 5,5′-diformyl-2,2′5′,2′-terfuran (3). Reduction of 2 and 3 afforded 5-hydroxymethyl-2,2′,5′,2
Publikováno v:
Archives of physical medicine and rehabilitation. 27
Publikováno v:
ChemInform. 27
Formylation of 2,2′,5′,2′-terfuran (1) with N-methylformanilide and phosphorus oxychloride gave 5-formyl-2,2′,5′,2′-terfuran (2) and 5,5′-diformyl-2,2′5′,2′-terfuran (3). Reduction of 2 and 3 afforded 5-hydroxymethyl-2,2′,5′,2
Autor:
L. Field, J. W. McFarland
Publikováno v:
Organic Syntheses
p-Toluenesulfonic anhydride reactant: 190 g. (1.0 mole) of p-toluenesulfonic acid monohydrate solvent: 400 ml. of ethylene chloride product: p-toluenesulfonic anhydride Keywords: elimination, dehydration; capillary, sealed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f647aff86fd0a656c797739bdfbdcf7
https://doi.org/10.1002/0471264180.os036.33
https://doi.org/10.1002/0471264180.os036.33
Publikováno v:
Lancet (London, England). 342(8863)
Akademický článek
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Publikováno v:
Journal of Heterocyclic Chemistry. 17:273-276
4-Toluenesulfonyl isocyanate (I) reacted with 2-aminoethanol and 3-amino-l-propanol to give 2:1 isocyanate/amino alcohol addition products. 1-Amino-2-propanol and I gave 1:1 and 2:1 adducts while 2-amino-2-methyl-l-propanol afforded only a 1:1 adduct
Publikováno v:
Journal of Heterocyclic Chemistry. 25:1431-1434
4-Toluenesulfonyl isocyanate cyclized with 1,2-epoxy-3-phenoxypropane and 2,3-epoxypropyl 4-methoxyphenyl ether, respectively, to give 3-(4-toluenesulfonyl)-5-phenoxymethylene-2-oxazolidone (I) and 3-(4-toluenesulfonyl)-5-(4-methoxyphenoxymethylene)-