Zobrazeno 1 - 10
of 95
pro vyhledávání: '"Dieter Wege"'
Publikováno v:
ChemistrySelect. 1:5339-5346
1,1-Dimethylcycloprop[e]azulene and 1,1-dimethylcycloprop[f]azulene derivatives were prepared through a short synthesis from thiophene-1,1-dioxides using a Houk-Leaver azulene synthesis. The strain caused by the fusion of the cyclopropane ring had no
Autor:
Lorraine A. Malaspina, Allan H. White, Dieter Wege, Michael B. Tolmie, Brian W. Skelton, Simon Grabowsky
Publikováno v:
Structural Chemistry.
Autor:
Lorraine A. Malaspina, Simon Grabowsky, Michael B. Tolmie, Brian W. Skelton, Dieter Wege, Allan H. White
Publikováno v:
Malaspina, Lorraine A.; White, Allan H.; Wege, Dieter; Tolmie, Michael B.; Skelton, Brian W.; Grabowsky, Simon (2017). Tautomerism in acyl-pyrazolones and in a novel photolysis product—importance and impact of the accurate localization of hydrogen atoms in crystal structures. Structural chemistry, 28(5), pp. 1343-1357. Springer 10.1007/s11224-017-1005-0
Acyl-pyrazolones exist in four different tautomeric forms (two keto and two enol) in crystal structures. Routine crystal structure refinements using an independent atom model and routine isolated-molecule calculations fail in locating the mobile hydr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f95d3a3c8cecf8e2d4d5359f6dcaddf
https://boris.unibe.ch/138430/1/046_Malaspina2017_StructChem.pdf
https://boris.unibe.ch/138430/1/046_Malaspina2017_StructChem.pdf
Publikováno v:
Tetrahedron. 65:4569-4577
The title natural product 1 , which possesses a new ring skeleton, has been synthesised by a sequence in which the key steps involve a tandem intramolecular Diels–Alder/reverse Diels–Alder reaction sequence. Thus 3-(2-furyl)-1,4-dimethoxynaphthal
Autor:
Dieter Wege, Riskiono Slamet
Publikováno v:
Tetrahedron. 63:12621-12628
Flash vacuum pyrolysis (fvp) of a number of substrates, prepared by hydrogenating adducts derived from dimethoxy- or ethylenedioxy-substituted benzynes and furan, affords isobenzofurandiones through retro-Diels–Alder expulsion of ethylene and C–O
Publikováno v:
European Journal of Organic Chemistry. 2007:1184-1195
This paper describes synthetic approaches to potential precursors to cyclopropazulenes, a novel class of nonbenzenoid cycloproparenes. The acid-catalysed transannular aldol reaction of 1,10-dibromobicyclo[8.1.0]undecane-3,8-dione (10) gives a single
Autor:
Matthew J. Piggott, Dieter Wege
Publikováno v:
Tetrahedron. 62:3550-3556
The synthesis of the title compound, which shares its skeleton with a number of biologically active natural products, is described. The key steps are construction of a 3,4-disubstituted furan by a tandem Diels–Alder-retro-Diels–Alder reaction of
Publikováno v:
Biochemical Pharmacology. 65:1215-1226
The aim of this investigation was to determine the mechanism of action of the nitrosophenylpyridine derivative of nifedipine ("nitrosonifedipine", NN) on Fe(II) transport into erythrocytes. Nifedipine is rapidly degraded to NN by daylight. We used ra
Autor:
Dieter Wege
Publikováno v:
European Journal of Organic Chemistry. 2001:849-862
Publikováno v:
ChemInform. 26
Alkylation of 2-furylmethanethiol (28) with propargyl chloride gave the thioether (22) which on methoxycarbonylation afforded the acetylenic ester (30). On heating, this material underwent an intramolecular Diels -Alder reaction to give the tricyclic