Výsledky vyhledávání - "ALLAN H. WHITE"

Akademický článek

Ilmu Kimia Tanaman Lauraceae Indonesia: VI. Kriptokaryon dari Cryptocarya Laevigata BL. (Lauraceae)

Autor: Sjamsul Arifin Achmad, Effendi Effendi, Emilio L. Ghisalberti, Euis Holisotan Hakim, Lia Dewi Juliawaty, Lukman Makmur, Allan H. White

Publikováno v: Journal of Mathematical and Fundamental Sciences, Vol 24, Iss 2/3 (2019)

Ekstraksi kulit akar dan kulit barang tanaman Cryptocarya laevigata Bl. (Lauraceae) dengan n-heksan menghasilkan suatu calkon yang diidentifikasi sebagai kriptokaryon (I). Struktur senyawa ini ditetapkan berdasarkan data spektroskopi dan analisis Kri

Externí odkaz: https://doaj.org/article/f55ce7b8d6c94827a3a4f0310dece7e2

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Akademický článek

Synthesis and X-ray Structural Studies of a Substituted 2,3,4,5-Tetrahydro-1H-3-benzazonine and a 1,2,3,5-Tetrahydro-4,3-benzoxazonine

Autor: Timothy S. Bailey, John B. Bremner, Brian W. Skelton, Allan H. White

Publikováno v: Molecules, Vol 20, Iss 1, Pp 487-502 (2014)

Using a common 1-(1-phenylethenyl)-1,2,3,4-tetrahydroisoquinoline precursor to the required ylide or N-oxide intermediate, the Stevens [2,3] and analogous Meisenheimer [2,3] sigmatropic rearrangements have been applied to afford concise syntheses of

Externí odkaz: https://doaj.org/article/eeeb0fe6f4354857a68bf77ec42b9895

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Akademický článek

Synthesis and Structural Characterization of 1-[2-(5-Nitro-1H-indol-2-yl)phenyl]methylpyridinium Chloride

Autor: John B. Bremner, Siritron Samosorn, Brian W. Skelton, Allan H. White

Publikováno v: Molecules, Vol 16, Iss 9, Pp 7627-7633 (2011)

In the course of studies on hybrid antibacterials incorporating 2-aryl-5-nitro-1H-indole moieties as potential bacterial NorA efflux pump inhibitors, the compound 1-[2-(5-nitro-1H-indol-2-yl)phenyl]methylpyridinium chloride (2) was synthesized and st

Externí odkaz: https://doaj.org/article/004921cd8e914c47a07135a8ec30d680

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Uranyl complexes of p-t-butylcalix[8]arene as H-bond acceptors—subtle effects of the donors

Autor: Mark I. Ogden, Alexandre N. Sobolev, Allan H. White, Jack Harrowfield

Publikováno v: Journal of Inclusion Phenomena and Macrocyclic Chemistry. 101:217-225

Leaving a mixture of excess N,N,N′,N′-tetramethyl-1,4-butanediamine (Me4BDA) with p-t-butylcalix[8]arene (L) and [(UO2)(dmso)5](ClO4)2 in a 1:2 ratio in acetonitrile solution to stand for an extended period resulted in the deposition of a mixture

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::13018268c7d9d8deab0dd49381c28d48
https://doi.org/10.1007/s10847-021-01075-5

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Synthesis and structural characterisation of some 1:1:2 complexes of silver(I) compounds with triphenylpnictides and 'ethylenediamine', [(Ph3E)(N-en)Ag(N-en-N')2Ag(N-en)(EPh3)]2+(X−)2

Autor: null Effendy, Fabio Marchetti, Corrado Di Nicola, Claudio Pettinari, Riccardo Pettinari, Brian W. Skelton, Alessia Tombesi, Allan H. White

Publikováno v: Inorganica Chimica Acta (Testo stamp.) 534 (2022): 120825-1–120825-8. doi:10.1016/j.ica.2022.120825
info:cnr-pdr/source/autori:Effendy; Marchetti F.; Di Nicola C.; Pettinari C.; Pettinari R.; Skelton B.W.; Tombesi A.; White A.H./titolo:Synthesis and structural characterisation of some 1:1:2 complexes of silver(I) compounds with triphenylpnictides and "ethylenediamine", [(Ph3E)(N-en)Ag(N-en-N')2Ag(N-en)(EPh3)]2+(X-)2/doi:10.1016%2Fj.ica.2022.120825/rivista:Inorganica Chimica Acta (Testo stamp.)/anno:2022/pagina_da:120825-1/pagina_a:120825-8/intervallo_pagine:120825-1–120825-8/volume:534

Colourless crystalline adducts obtained by the crystallization of various silver(I) compounds in 1:1 M proportions with EPh3 (E = P, As, Sb) from 1,2-diaminoethane (ethylenediamine) (en ? H2N(CH2)2NH2) have been structurally characterized by room tem

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd2c018c4cb3cbcad394bafb440ad0ec
https://hdl.handle.net/11581/457336

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Synthesis and structural characterization of some 1:1 adducts of silver(I) salts with (hindered) PR3 bases (R = phenyl, o-tolyl, cyclohexyl)

Autor: null Effendy, Corrado Di Nicola, Peter C. Healy, Fabio Marchetti, Claudio Pettinari, Brian W. Skelton, Alessia Tombesi, Allan H. White

Publikováno v: Inorganica Chimica Acta. 536:120895

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b132c473149f056e43b3f165598551f1
https://doi.org/10.1016/j.ica.2022.120895

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Synthesis and structural characterisation of four 1:1:2 ionic/mononuclear complexes of Ag(I) and Cu(I) salts with tertiary organophosphine and 1,2-diamines

Autor: null Effendy, Fabio Marchetti, Robert D. Hart, Claudio Pettinari, Brian W. Skelton, Alessia Tombesi, Allan H. White

Publikováno v: Inorganica Chimica Acta. 536:120882

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::04b7906028e13275ac84359ee2576578
https://doi.org/10.1016/j.ica.2022.120882

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Synthesis and structural characterisation of some mononuclear 1:1:1 complexes of coinage metal(I) compounds with tertiary phosphines (arsines) and 1,2-diamines, [MX(EPh3)(N,N'-1,2-diamine)]

Autor: Brian W. Skelton, Allan H. White, Riccardo Pettinari, Corrado Di Nicola, Robert D. Hart, Effendy, Claudio Pettinari, Fabio Marchetti

Publikováno v: Inorganica Chimica Acta (Testo stamp.) 517 (2021). doi:10.1016/j.ica.2020.120185
info:cnr-pdr/source/autori:Di Nicola C.; Effendy; Hart R.D.; Marchetti F.; Pettinari C.; Pettinari R.; Skelton B.W.; White A.H./titolo:Synthesis and structural characterisation of some mononuclear 1:1:1 complexes of coinage metal(I) compounds with tertiary phosphines (arsines) and 1,2-diamines, [MX(EPh3)(N,N'-1,2-diamine)]/doi:10.1016%2Fj.ica.2020.120185/rivista:Inorganica Chimica Acta (Testo stamp.)/anno:2021/pagina_da:/pagina_a:/intervallo_pagine:/volume:517

Crystallization of adducts of simple copper(I) and silver(I) salts (MX) with triphenylphosphine from 'N,N,N′,N'-tetramethylethylenediamine', 'tmeda', has yielded adducts of 1:1:1 MX:PPh3:tmeda stoichiometry, all of which have been characterized by

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2172b4e44eacf8cff0842d3c0832078
https://publications.cnr.it/doc/443644

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