Zobrazeno 1 - 10 of 22 pro vyhledávání: '"J. W. Ziller"'
1
ChemInform Abstract: Synthesis and Reactivity of 1,2-Dioxolanes from β,γ-Epoxy Ketones
Autor: J. W. Ziller, Chunhua Hu, K. A. Woerpel, Curtis J. Rieder, Andrew M. Thomas, Wynne V. Kandur, Kathleen J. Richert
Publikováno v: ChemInform. 45
A single step acid-catalyzed addition of H2O2 to β,γ-epoxy ketones is developed to synthesize hydroperoxy-substituted 1,2-dioxolanes as mixture of diastereomers.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1fa527ba6025972d15742afc00d19db4
https://doi.org/10.1002/chin.201441133
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2
Synthesis and reactivity of 1,2-dioxolanes from β,γ-epoxy ketones
Autor: Kathleen J. Richert, Chunhua Hu, J. W. Ziller, K. A. Woerpel, Andrew M. Thomas, Wynne V. Kandur, Curtis J. Rieder
Publikováno v: Organic letters. 16(10)
Five-membered ring peroxides were prepared in one step in 31–86% yield from readily accessible β,γ-epoxy ketones and H2O2. The reaction proceeded via a tetrahydrofuran, which was converted to the thermodynamically favored 1,2-dioxolane. The produ
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1698f0f3b68c926cfe5751bfb224ffc3
https://pubmed.ncbi.nlm.nih.gov/24779430
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4
ChemInform Abstract: (1Z,3Z)-1,4-Diphenyl-1,4-bis(3-chlorophenylmethylthio)buta-1,3-diene
Autor: J. W. Ziller, F. Freeman, Hengyao Lu
Publikováno v: ChemInform. 27
The crystal structure of the title compound, C 30 H 24 Cl 2 S 2 , (I), is described and compared with that of (1Z,3Z)-1,4-diphenyl-1,4-bis(p-tolylmethylthio)buta-1,3-diene, (II). The 1,3-butadiene moiety in compound (I) has a planar s-trans conformat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::87271858473d71bb5456da6ba00e0958
https://doi.org/10.1002/chin.199638030
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7
ChemInform Abstract: Relative and Absolute Configuration of Aloperine
Autor: Q. Zhang, A. D. Brosius, J. W. Ziller
Publikováno v: ChemInform. 29
The relative and absolute configuration of the title compound, (6R,7R,9R,11S)-16,17-didehydro-9-de-2-piperidinylormosanine, C15H24N2, has been elucidated. Two X-ray structures, one of the free base of the alkaloid and the second of its dihydrochlorid
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::937d473f8fab713411d64a2d7c8c05b2
https://doi.org/10.1002/chin.199807029
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