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Organic Letters|February 10, 2007
Conjugate addition of 2- and 4-pyridylcuprates: an expeditious asymmetric synthesis of natural (-)-evoninic acidAlan C Spivey, Lena Shukla, Judy F HaylerOrganic Letters|November 17, 2010
"One-pot" tandem C-H borylation/1,4-conjugate addition/reduction sequenceHazmi Tajuddin, Lena Shukla, Aoife C Maxwell, et al.Dalton Transactions (Cambridge, England : 2003)|July 15, 2004
Early-late, mixed-metal compounds supported by amidophosphine ligandsQ Folashade Mokuolu, Paul A Duckmanton, Peter B Hitchcock, et al.Journal of Medicinal Chemistry|July 9, 2013
Discovery of potent, isoform-selective inhibitors of histone deacetylase containing chiral heterocyclic capping groups and a N-(2-aminophenyl)benzamide binding unitCharles M Marson, Christopher J Matthews, Elena Yiannaki, et al.European Journal of Medicinal Chemistry|March 19, 2016
2,8-Diazaspiro[4.5]decan-8-yl)pyrimidin-4-amine potent CCR4 antagonists capable of inducing receptor endocytosisLena Shukla, Laura A Ajram, Malcolm Begg, et al.Organic & Biomolecular Chemistry|August 14, 2014
Iridium-catalyzed C-H borylation of pyridinesScott A Sadler, Hazmi Tajuddin, Ibraheem A I Mkhalid, et al.Bioorganic & Medicinal Chemistry Letters|September 12, 2020
Structure-based optimisation of orally active & reversible MetAP-2 inhibitors maintaining a tight 'molecular budget'David J Hirst, Martin Brandt, Gordon Bruton, et al.Pageof 1