Hasan Palandoken, Ph.D. - Publications

Affiliations: 
2006 University of California, Davis, Davis, CA 

7 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Bellinghiere AT, Doherty EE, Pistel WL, Browne JE, Palandoken H. A facile synthesis of O-[(3-methyloxetan-3-yl)-methyl]hydroxylamine Organic Preparations and Procedures International. 47: 232-235. DOI: 10.1080/00304948.2015.1025624  0.92
2014 Ewan HS, Muli CS, Touba S, Bellinghiere AT, Veitschegger AM, Smith TB, Pistel WL, Jewell WT, Rowe RK, Hagen JP, Palandoken H. Synthesis of sugar oxime ether surfactants Tetrahedron Letters. 4962-4965. DOI: 10.1016/j.tetlet.2014.07.036  0.92
2010 Harley W, Floyd C, Dunn T, Zhang XD, Chen TY, Hegde M, Palandoken H, Nantz MH, Leon L, Carraway KL, Lyeth B, Gorin FA. Dual inhibition of sodium-mediated proton and calcium efflux triggers non-apoptotic cell death in malignant gliomas. Brain Research. 1363: 159-69. PMID 20869350 DOI: 10.1016/j.brainres.2010.09.059  0.92
2005 Palandoken H, By K, Hegde M, Harley WR, Gorin FA, Nantz MH. Amiloride peptide conjugates: prodrugs for sodium-proton exchange inhibition. The Journal of Pharmacology and Experimental Therapeutics. 312: 961-7. PMID 15509720 DOI: 10.1124/jpet.104.076984  0.92
2005 Palandoken H, Bocian CM, McCombs MR, Nantz MH. A facile synthesis of (tert-alkoxy)amines Tetrahedron Letters. 46: 6667-6669. DOI: 10.1016/j.tetlet.2005.07.149  0.92
1999 Palandoken H, Wyatt JK, Hitchcock SR, Olmstead MM, Nantz MH. Reductive dehydroxy coupling of 2-(hydroxymethyl)indenes to prepare ethano-bridged bis(2-indenyl) ansa-titanocenes Journal of Organometallic Chemistry. 579: 338-347.  0.92
1996 Palandoken H, McMillen WT, Nantz MH. An improved synthesis of 2-(hydroxymethyl)indene Organic Preparations and Procedures International. 28: 702-704.  0.92
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