Gregory R. Dake, Ph.D.
|Chemistry||University of British Columbia, Vancouver, Vancouver, BC, Canada|
Area:Synthetic Organic and Organometallic
Google:"Greg Dake UBC"
Mean distance: 7.16
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|Serin SC, Dake GR, Gates DP. (2016) Phosphaalkene-oxazoline copolymers with styrene as chiral ligands for rhodium(i). Dalton Transactions (Cambridge, England : 2003)|
|Castillo-Contreras EB, Dake GR. (2014) DMAP promoted tandem addition reactions forming substituted tetrahydroxanthones Organic Letters. 16: 1642-1645|
|Serin SC, Patrick BO, Dake GR, et al. (2014) Reaction of an enantiomerically pure phosphaalkene-oxazoline with MeM nucleophiles (M = Li and MgBr): Stereoselectivity and noninnocence of the P-mesityl substituent Organometallics. 33: 7215-7222|
|Castillo-Contreras EB, Stahl AM, Dake GR. (2014) Annulated isoxazoles via [3 + 2] cycloaddition of alkenyl bromides and oximoyl chlorides and Ag(I) promoted elimination Journal of Organic Chemistry. 79: 7250-7255|
|Vilin YY, Nunez JJ, Kim RY, et al. (2013) Paradoxical activation of an inwardly rectifying potassium channel mutant by spermine: "(B)locking" open the bundle crossing gate Molecular Pharmacology. 84: 572-581|
|Sala-Rabanal M, Li DC, Dake GR, et al. (2013) Polyamine transport by the polyspecific organic cation transporters OCT1, OCT2, and OCT3. Molecular Pharmaceutics. 10: 1450-8|
|Loosley BC, Andersen RJ, Dake GR. (2013) Total synthesis of cladoniamide G. Organic Letters. 15: 1152-4|
|Dugal-Tessier J, Serin SC, Castillo-Contreras EB, et al. (2012) Enantiomerically pure phosphaalkene-oxazolines (PhAk-Ox): synthesis, scope and copolymerization with styrene. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 6349-59|
|Dake GR. (2012) Enamides and related functional groups as nucleophilic components in ring-forming processes catalyzed by electrophilic metal salts Synlett. 23: 814-824|
|Dugal-Tessier J, Conrad ED, Dake GR, et al. (2012) Phosphaalkenes Phosphorus(Iii) Ligands in Homogeneous Catalysis: Design and Synthesis. 321-341|