Year |
Citation |
Score |
2016 |
Wilkinson FL, Mahmoud A, Jones AM, Wilkinson J, Romero M, Duarte J, Alexander MY. 204 Glycomimetics; A Novel Class of Drugs to Protect Against Free Fatty Acid-Induced Endothelial Dysfunction Heart. 102. DOI: 10.1136/Heartjnl-2016-309890.204 |
0.33 |
|
2016 |
Wilkinson FL, Mahmoud AM, Jones A, Wilkinson JA, Romero M, Duarte J, Alexander MY. A new class of glycomimetic drugs to prevent free fatty acid-induced endothelial dysfunction Cardiovascular Research. 111. DOI: 10.1093/Cvr/Cvw149 |
0.335 |
|
2016 |
Killoran PM, Rossington SB, Wilkinson JA, Hadfield JA. Expanding the scope of the Babler–Dauben oxidation: 1,3-oxidative transposition of secondary allylic alcohols Tetrahedron Letters. 57: 3954-3957. DOI: 10.1016/J.Tetlet.2016.07.076 |
0.302 |
|
2015 |
Mahmoud AM, Wilkinson FL, Jones AM, Wilkinson JA, Romero M, Duarte J, Alexander MY. 43 A novel role for small molecule glycomimetics in the protection against lipid-induced endothelial dysfunction Heart. 101. DOI: 10.1136/Heartjnl-2015-308734.43 |
0.33 |
|
2015 |
Gooch LM, Rossington SB, Wilkinson JA. Asymmetric synthesis of diarylmethane derivatives by dynamic kinetic resolution Tetrahedron Letters. 56: 4025-4027. DOI: 10.1016/J.Tetlet.2015.05.006 |
0.342 |
|
2013 |
Slabu I, Rossington SB, Killoran PM, Hirst N, Wilkinson JA. Total synthesis of (±)-mimosifoliol by lateral lithiation Tetrahedron Letters. 54: 1489-1490. DOI: 10.1016/J.Tetlet.2013.01.040 |
0.353 |
|
2010 |
Lagoutte R, Wilkinson JA. A novel one-step method for the reductive allylation of esters and the first total synthesis of (±)-erythrococcamide B Tetrahedron Letters. 51: 6942-6944. DOI: 10.1016/J.Tetlet.2010.10.159 |
0.34 |
|
2008 |
Wilkinson JA, Raiber EA, Ducki S. New stabilising groups for lateral lithiation of ortho-cresol derivatives and a new route to 2-substituted chromans Tetrahedron. 64: 6329-6333. DOI: 10.1016/J.Tet.2008.04.093 |
0.358 |
|
2007 |
Wilkinson JA, Rossington SB, Coe NA, Hirst N, McGown AT, Leonard J, Hussain N. Synthesis and evaluation of 2'-substituted fendiline analogues as antileukemics Letters in Drug Design and Discovery. 4: 246-248. DOI: 10.2174/157018007784620068 |
0.325 |
|
2007 |
Wilkinson JA, Ardes-Guisot N, Ducki S, Leonard J. Novel methods for the synthesis of 5-substituted-3-carboxy-2,5- and 4,5-dihydrothiophenes and 5-substituted 2- and 3-sulfolenes Tetrahedron. 63: 1065-1073. DOI: 10.1016/J.Tet.2006.11.061 |
0.392 |
|
2006 |
Wilkinson JA, Rossington SB, Ducki S, Leonard J, Hussain N. Asymmetric alkylation of diarylmethane derivatives Tetrahedron. 62: 1833-1844. DOI: 10.1016/J.Tet.2005.11.044 |
0.401 |
|
2005 |
Wilkinson JA, Ardes-Guisot N, Ducki S, Leonard J. Towards the total synthesis of tangutorine by intramolecular Diels-Alder reaction Tetrahedron Letters. 46: 8053-8056. DOI: 10.1016/J.Tetlet.2005.09.058 |
0.357 |
|
2004 |
Wilkinson JA, Rossington SB, Leonard J, Hussain N. Asymmetric alkylation of diarylmethane derivatives. Improved results using methoxyethoxy substituent Tetrahedron Letters. 45: 5481-5483. DOI: 10.1016/J.Tetlet.2004.05.058 |
0.409 |
|
2004 |
Wilkinson JA, Rossington SB, Leonard J, Hussein N. Asymmetric alkylation of diphenylmethane derivatives using (-)-sparteine Tetrahedron Letters. 45: 1191-1193. DOI: 10.1016/J.Tetlet.2003.11.138 |
0.391 |
|
2004 |
Wilkinson JA, Rossington SB, Ducki S, Leonard J, Hussain N. Asymmetric alkylation of N-pivaloyl-o-benzylaniline Tetrahedron Asymmetry. 15: 3011-3013. DOI: 10.1016/J.Tetasy.2004.08.020 |
0.336 |
|
1995 |
Muxworthy JP, Wilkinson JA, Procter G. Stereoselective cycloadditions of chiral acyl-nitroso compounds; palladium(0) catalyzed allylic displacement with concomitant loss of the chiral auxiliary Tetrahedron Letters. 36: 7541-7544. DOI: 10.1016/0040-4039(95)01527-2 |
0.399 |
|
1995 |
Muxworthy JP, Wilkinson JA, Procter G. Stereoselective cycloadditions of chiral acyl-nitroso compounds; unexpected formation of an oxazolidinone Tetrahedron Letters. 36: 7539-7540. DOI: 10.1016/0040-4039(95)01526-4 |
0.386 |
|
1995 |
Muxworthy JP, Wilkinson JA, Procter G. Stereoselective cycloadditions of chiral acyl-nitroso compounds; hydrolytic reactions of a clyclopentadiene adduct Tetrahedron Letters. 36: 7535-7538. DOI: 10.1016/0040-4039(95)01525-6 |
0.38 |
|
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