Dr. Frank Edward Mcdonald M.D.
Physiatrist (Physical Medicine) | Pediatric Rehabilitation Medicine
3301 Swiss Ave Dallas TX, 75204About
Dr. Frank Mcdonald is a physiatrist practicing in Dallas, TX. Dr. Mcdonald is a medical doctor specializing in physical medicine and rehabilitation. As a physiatrist, Dr. Mcdonald focuses on a patients ability to function, and can treat multiple conditions that affect the brain, nerves, spine, bones, muscles, joints, ligaments and tendons. Dr. Mcdonald can diagnose and treat pain that is a result of injury, disease or a disabling condition. Physiatrists often lead a team of physical therapists, occupational therapists and physicians in a patients treatment or prevention plan.
Board Certification
PediatricsAmerican Board of PediatricsABP
Physical Medicine and RehabilitationAmerican Board of Physical Medicine and RehabilitationABPMR- Pediatric Rehabilitation Medicine
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Concise, regioselective synthesis of the ABC tristetrahydropyran of thyrsiferol and venustatriol.
- Synthesis of monodisperse oligo-p-phenylenes via rhodium-catalyzed alkyne cyclotrimerization.
- Stereoselective synthesis of vancosamine and saccharosamine glycals via tungsten-catalyzed alkynol cycloisomerization.
- Computational studies of tungsten-catalyzed endo-selective cycloisomerization of 4-pentyn-1-ol.
- Endo-oxacyclizations of polyepoxides: biomimetic synthesis of fused polycyclic ethers.
- Stereoselective synthesis of a family of alternating polyols from six-carbon epoxyalkynol modules.
- Stereoselective synthesis of L-oliose trisaccharide via iterative alkynol cycloisomerization and acid-catalyzed glycosylation.
- Biomimetic synthesis of fused polypyrans: oxacyclization stereo- and regioselectivity is a function of the nucleophile.
- Organolanthanide-catalyzed intramolecular hydroamination/cyclization/bicyclization of sterically encumbered substrates. Scope, selectivity, and catalyst thermal stability for amine-tethered unactivated 1,2-disubstituted alkenes.
- Total synthesis of the polyene-polyol macrolide RK-397, featuring cross-couplings of alkynylepoxide modules.
- Stereoselective synthesis of d-desosamine and related glycals via tungsten-catalyzed alkynol cycloisomerization.
- Synthesis of seven-membered ring glycals via endo-selective alkynol cycloisomerization.
- Alkene substituents for selective activation of endo-regioselective polyepoxide oxacyclizations.
- Biomimetic synthesis of trans,syn,trans-fused polyoxepanes: remarkable substituent effects on the endo-regioselective oxacyclization of polyepoxides.
- 1-Deoxy-5-hydroxysphingolipids as new anticancer principles: an efficient procedure for stereoselective syntheses of 2-amino-3,5-diols.
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