Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Lynne Horsburgh"'
Autor:
Mark R. J. Elsegood, Shahzad Riaz, Simon J. Teat, Lynne Horsburgh, Thomas G. Warwick, Mark Edgar, George W. Weaver
Publikováno v:
Crystal Growth & Design. 19:5237-5248
The effect of varying the chain length on the solid state conformation and packing of 6,12-dialkoxy- and 6,12-dialkylsulfanyl-benzo[1,2-b:4,5-b’]bis[b]benzothiophenes has been studied. The compounds were prepared by SNAr reaction of 6,12-difluorben
Publikováno v:
ChemistrySelect. 2:759-768
Reaction of LiOR (R=t-Bu, Ph) with the acids 2,2/-Ph2C(X)(CO2H), X=OH (benzH), NH2 (dpgH) was investigated. For benzH, one equivalent LiOt-Bu in THF afforded [Li(benz)]2⋅2THF (1⋅2THF), which adopts a 1D chain structure. If acetonitrile is used (m
Autor:
Mark R. J. Elsegood, Carl Redshaw, Jung-Hee Do, Xing Feng, Tahmina Akther, Takehiko Yamato, Lynne Horsburgh, Chuan-Zeng Wang
Publikováno v:
Tetrahedron. 73:307-312
In this work, four stable dithieno[3,2-b:2',3'-d]thiophene-based π-extended molecules were designed and synthesized via a Pd-catalysed Sonogashira coupling reaction. The structures of these symmetrical compounds, including dithieno[3,2-b:2',3'-d]thi
Autor:
Xing Feng, Hirotsugu Tomiyasu, Lynne Horsburgh, Carl Redshaw, Mark R. J. Elsegood, Xian-Fu Wei, Simon J. Teat, Jian-Yong Hu, Takehiko Yamato
Publikováno v:
The Journal of Organic Chemistry. 80:10973-10978
This article presents a novel asymmetrical functionalization strategy for the construction of dipolar molecules via efficient regioselective functionalization along the Z-axis of pyrene at both the 1,3- and 6,8-positions. Three asymmetrically substit
Autor:
Jian-Yong Hu, Carl Redshaw, Takehiko Yamato, Hirotsugu Tomiyasu, Xing Feng, Mark R. J. Elsegood, Zhu Tao, Lynne Horsburgh, Simon J. Teat, Xian-Fu Wei
Publikováno v:
RSC Advances. 5:8835-8848
The present work probes the bromination mechanism of 2-tert-butylpyrene (1), which regioselectively affords mono-, di-, tri- and tetra-bromopyrenes, by theoretical calculation and detailed experimental methods. The bromine atom may be directed to the
Publikováno v:
Crystal Growth & Design. 14:270-277
Solvothermal reactions of the lower-rim functionalized diacid calix[4]arene 25,27-bis(methoxycarboxylic, acid)-26,28-dihydroxy-4-tert-butylcalix[4]arene, (LH2) with Zn(NO3)2·6H2O and the dipyridyl ligands 4,4′-bipyridyl (4,4′-bipy), 12-di(4-pyri
Autor:
Vladimír Kryštof, Mark R. J. Elsegood, Simon J. Teat, Mariam Mojally, Mark Edgar, George W. Weaver, Lynne Horsburgh, Paul D. Lucas, Fatemeh Zeinali, Thomas G. Warwick, Avninder S. Bhambra
The file attached to this record is the author's final peer reviewed version. The Publisher's final version can be found by following the DOI link. A small library of twelve, structurally diverse, fluoroaryl benzimidazoles was prepared using a simple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d853fc090d09a3e9c713b19fe3d9eff
https://doi.org/10.1016/j.jfluchem.2016.06.009
https://doi.org/10.1016/j.jfluchem.2016.06.009
Autor:
Lynne Horsburgh, William Clegg, Alan Robertson, Fiona M. Mackenzie, Robert E. Mulvey, Stephen T. Liddle
Publikováno v:
Journal of the Chemical Society, Dalton Transactions. :1225-1231
A family of crystalline lithium anilide solvates, [{PhN(H)Li·(pyr)2}2] 1, [{PhN(H)Li·(4-Me-pyr)2}2] 2 and [{PhN(H)Li}4·(4-But-pyr)6] 3 has been synthesised by reacting the aromatic primary amide with two molar equivalents of the appropriate pyridi
Autor:
D.Vaughan Griffiths, Mark R. J. Elsegood, Dominic A. Davies, John R. Miller, Laila S. Ahmed, Lynne Horsburgh, Nigel Wheatley, Jonathan R. Dilworth, William Clegg
Publikováno v:
Polyhedron. 18:593-600
Novel substituted benzenethiols can be easily prepared via aryl thiocyanates or arylbromides. Reaction of [(Ph3P)AuCl] with the sterically-non demanding benzenethiols HSC6H4NMe2-p and HSC6H4NMe3+-p and with the sterically-demanding benzenethiols HSCM
Autor:
Michael J. Ross, William Clegg, Robert E. Mulvey, RenéB. Rowlings, Victoria Wilson, Lynne Horsburgh
Publikováno v:
Polyhedron. 17:1923-1930
Three new magnesium diamide complexes have been prepared by treating the diamine precursors N,N'-diphenylethylenediamine or N,N'-dibenzylethylenediamine with the commercial reagent dibutyl-magnesium in the presence of a donor solvent (THF or HMPA). T