

{"id":12,"date":"2020-08-10T13:30:27","date_gmt":"2020-08-10T17:30:27","guid":{"rendered":"https:\/\/sites.temple.edu\/facultyviscoustemplate\/?page_id=12"},"modified":"2025-03-02T11:53:29","modified_gmt":"2025-03-02T16:53:29","slug":"curriculum-vitae","status":"publish","type":"page","link":"https:\/\/sites.temple.edu\/daltongroup\/curriculum-vitae\/","title":{"rendered":"Curriculum Vitae"},"content":{"rendered":"<h4>David Robert Dalton<\/h4>\n<p><a href=\"https:\/\/sites.temple.edu\/daltongroup\/files\/2022\/12\/dalton6cor.-1.gif\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-173 size-full\" src=\"https:\/\/sites.temple.edu\/daltongroup\/files\/2022\/12\/dalton6cor.-1.gif\" alt=\"\" width=\"157\" height=\"208\"><\/a><\/p>\n<h6><strong>EDUCATION and POSITIONS HELD:<\/strong><\/h6>\n<hr>\n<p><a href=\"http:\/\/northwestern.edu\/\">Northwestern University<\/a>, Evanston, IL, B.A. (with Honors), <b>1957<\/b>.<\/p>\n<p><a href=\"http:\/\/ucla.edu\/\"> University of California<\/a>, Los Angeles, CA, Ph.D., <b>1962<\/b>.<\/p>\n<p><b>1962-1964 <\/b> Research Chemist, Monsanto Research Corporation Dayton Laboratories. A division of the <a href=\"http:\/\/www.monsanto.com\/\">Monsanto Company<\/a> (acquired by <a href=\"https:\/\/www.bayer.com\/en\/\">Bayer <\/a> in 2018).<\/p>\n<p><b>1964-1965 <\/b> Instructor and <a href=\"http:\/\/www.nih.gov\/\"> National Institutes of Health<\/a>, Postdoctoral Fellow, <a href=\"http:\/\/www.osu.edu\/\">The Ohio State University<\/a>, Columbus, Ohio<\/p>\n<p><b>1965 <\/b> &#8211; present, <a href=\"http:\/\/www.temple.edu\"> Temple University <\/a>, Philadelphia, PA.<\/p>\n<h6><strong>VISITING PROFESSORSHIPS:<\/strong><\/h6>\n<hr>\n<p><b>1972-1973<\/b> <a href=\"http:\/\/www.technion.ac.il\/\">Israel Institute of Technology (Technion), <\/a> Haifa, Israel<\/p>\n<p><b>1976-1977<\/b> <a href=\"http:\/\/www.yale.edu\/\">Yale University<\/a>, New Haven, Connecticut<\/p>\n<p><b>1988-1989<\/b> <a href=\"http:\/\/www.brynmawr.edu\/\">Bryn Mawr College<\/a>, Bryn Mawr, Pennsylvania<\/p>\n<p><b>1992<\/b> Visiting Master Teacher in Residence, <a href=\"http:\/\/www.clemson.edu\/\"> Clemson University,<\/a> Clemson, South Carolina.<\/p>\n<hr>\n<p><strong>NAME SPECIAL AWARDS RECEIVED FOR TEACHING EXCELLENCE:<\/strong><\/p>\n<hr>\n<ul>\n<li>The Christian R. and Mary F. Lindback Foundation Award for Distinguished Teaching, <a href=\"http:\/\/www.temple.edu\/\">Temple University<\/a>, <b>1975 <\/b>.<\/li>\n<li style=\"text-align: left\">The College of Arts and Sciences Alumni Award for Excellence in Teaching, <a href=\"http:\/\/www.temple.edu\/\">TempleUniversity<\/a>, <b>1986<\/b>.<\/li>\n<li style=\"text-align: left\"><a href=\"http:\/\/www.theaic.org\">American Institute of Chemists<\/a>, Philadelphia Area, Scroll Awardee, May, <b>1989<\/b>.<\/li>\n<li style=\"text-align: left\">Visiting Master Teacher in Residence,<a href=\"http:\/\/www.clemson.edu\/\"> Clemson University<\/a>, Clemson, S.C., <b>1994<\/b>.<\/li>\n<li style=\"text-align: left\">The Great Teacher Award, <a href=\"http:\/\/www.temple.edu\">Temple University<\/a>, <b>1997<\/b>.<\/li>\n<li style=\"text-align: left\"><a href=\"http:\/\/phillyacs.org\">The Philadelphia Section<\/a> of the <a href=\"http:\/\/www.acs.org\">American Chemical Society<\/a> Award (Sponsored by <a href=\"http:\/\/www.merck.com\"> Merck,<\/a> Inc.) for &#8220;Excellence in Teaching Undergraduate Chemical Science,&#8221; <b>2003<\/b><\/li>\n<li style=\"text-align: left\">Honors Professor of the Year, <b>2005<\/b>. Voted by the students of the <a href=\"http:\/\/www.temple.edu\/honors\/\"> Temple University Honors Program <\/a>.<\/li>\n<\/ul>\n<h5>PUBLICATIONS:<\/h5>\n<hr>\n<p><strong>BOOKS PUBLISHED OR IN PRESS:<\/strong><\/p>\n<hr>\n<ul>\n<li>D. R. Dalton, <i>The Alkaloids: The Fundamental Chemistry &#8211; A Biogenetic Approach<\/i>.<a href=\"http:\/\/www.dekker.com\/\"> M. Dekker, Inc.<\/a>, New York (<b>1979<\/b>).<\/li>\n<li>M. T. Yip and D. R. Dalton, <i>Organic Chemistry in The Laboratory<\/i>. D. van Nostrand Company, New York, (<b>1979<\/b>).<\/li>\n<li>Dalton, David R. <i> Foundations of Organic Chemistry: Unity and Diversity of Structures, Pathways, and Reactions<\/i>,<a href=\"https:\/\/www.wiley.com\"> Wiley-VCH Publishers <\/a>, New York (<b>2011<\/b>). ISBN 978-0-470-47908-7.<\/li>\n<li>Dalton, David R. <i>The Chemistry of Wine<\/i>. <a href=\"https:\/\/global.oup.com\/academic\/product\/the-chemistry-of-wine-9780190687199?q=Dalton%20Chemistry%20of%20Wine&amp;lang=en&amp;cc=us\"> Oxford University Press <\/a>, New York (<b>2017<\/b>), ISBN 978-0-19-068719-9.<\/li>\n<li>Dalton, David R. <i> Foundations of Organic Chemistry: Unity and Diversity of Structures, Pathways, and Reactions<\/i>, 2nd edition. <a href=\"https:\/\/www.wiley.com\"> Wiley-VCH Publishers<\/a>, New York (<b>2020<\/b>). Print ISBN: 978-1-119-65642-5 and eBook ISBN: 978-1-119-65643-2.<\/li>\n<\/ul>\n<hr>\n<p><strong>RESEARCH ARTICLES PUBLISHED OR IN PRESS:<\/strong><\/p>\n<hr>\n<ul>\n<li>Summerbell, R.K.; Berlingame, A.L.; Dalton, D.R.; Dalton, C.K. &#8220;The Dimethyl-<i>p<\/i>-dioxanes and the 2,5-Dibutyl-<i>p<\/i>-dioxanes,&#8221; <a href=\"http:\/\/pubs.acs.org\/journals\/joceah\/index.html\"><i>J. Org. Chem. <\/i><\/a><b>1962 <\/b>, <i>27<\/i>, 4365 (doi:10.1021\/jo01059a055).<\/li>\n<li>Dalton, D.R.; Cava, M.P.; Buck, K.T. &#8220;Hindered Rotation in l-Benzyl-1,2,3,4-tetrahydro-6,7-dimethoxyisoquinolines&#8221;,<a href=\"http:\/\/oxford.elsevier.com\/tis\/\"> <i>Tetrahedron Lett.<\/i><\/a> <b>1965<\/b>, <i>6<\/i> 2687 (10.1016\/S0040-4039(01)99526-7).<\/li>\n<li>Cava, M.P.; Wilkins, Jr., C.K.; Dalton, D.R.; Bessho, K. &#8220;A New Isoquinuclidine Synthesis. A New Route to <i>dl<\/i>-Dioscorone&#8221;, <a href=\"http:\/\/pubs.acs.org\/journals\/joceah\/index.html\"><i>J. Org. Chem.<\/i><\/a> <b>1965<\/b>, <i>30<\/i>, 3772 (doi:10.1021\/jo01022a042).<\/li>\n<li>Shamma, M.; Dudock, B.S.; Cava, M.P.; Rao, K.V.; Dalton, D.R.; DeJongh, D.C.; Schraeder, S.R. &#8220;Revised Structures of Hernandezine and Thalsimine. Mass Spectrometry of a Bisbenzylisoquinoline Alkaloid&#8221;,<a href=\"http:\/\/www.rsc.org\/is\/journals\/current\/chemcomm\/cccpub.htm\"> <i> Chemical Communications<\/i><\/a> <b>1966<\/b>, 7 (doi:10.1039\/C19660000007).<\/li>\n<li>Cava, M.P.; Dalton, D.R. &#8220;An Improved Synthesis of <i>dl<\/i>-Anonaine&#8221;,<a href=\"http:\/\/pubs.acs.org\/journals\/joceah\/index.html\"> <i>J. Org. Chem. <\/i><\/a><b>1966,<\/b> <i>31<\/i>, 1281 (doi:10.1021\/jo01342a507).<\/li>\n<li>Dalton, D.R.; Hendrickson, J.B.; Jones, D.G. &#8220;An Improved Procedure for the Preparation of Bromohydrins&#8221;, <a href=\"http:\/\/www.rsc.org\/is\/journals\/current\/chemcomm\/cccpub.htm\"><i>Chemical Communications <\/i><\/a><b>1966<\/b>, 591 (doi:10.1039\/C19660000591).<\/li>\n<li>Fraenkel, G.; Cava, M.P.; Dalton, D.R. &#8220;Hindered Rotation in l-Benzyl-1,2,3,4-tetrahydro-6,7-dimethoxyisoquinolines&#8221;,<a href=\"http:\/\/pubs.acs.org\/journals\/jacsat\/index.html\"> <i>J. Am. Chem. Soc.<\/i><\/a><b> 1967<\/b>,<i> 89<\/i>, 329 (doi:10.1021\/ja00978a027).<\/li>\n<li> Dalton. D.R.; Jones, D.G. &#8220;Halohydrin Formation in Dimethyl Sulfoxide&#8221;,<a href=\"http:\/\/oxford.elsevier.com\/tis\/\"> <i> Tetrahedron Lett.<\/i><\/a><b> 1967<\/b>, <i>8<\/i>, 2857 (doi:10.1016\/S0040-4039(00)90878-5).<\/li>\n<li>Dalton, D.R.; Liebman, S.A.; Waldman, H.; Sheinson, R.S.&#8221;ESR Detection of the Diphenylmethyl Radical&#8221;,<a href=\"http:\/\/oxford.elsevier.com\/tis\/\"> <i>Tetrahedron Lett.<\/i><\/a><b> 1968<\/b>, <i>9<\/i>, 145 (doi:1016\/S0040-4039(00)75576-6).<\/li>\n<li>Dalton, D.R.; Dutta, V.P.; Jones, D.G. &#8220;Bromohydrin Formation in Dimethyl Sulfoxide&#8221;,<a href=\"http:\/\/pubs.acs.org\/journals\/jacsat\/index.html\"> <i> J. Am. Chem. Soc.<\/i><\/a> <b>1968<\/b>, <i>90<\/i>, 5498 (doi:10.1021\/ja01022a030).<\/li>\n<li>Dalton, D.R.; Liebman, S.A. &#8220;Electron Spin Resonance Studies On Neutral Hydrocarbon Radicals&#8221;,<a href=\"http:\/\/pubs.acs.org\/journals\/jacsat\/index.html\"> <i>J. Am. Chem. Soc.<\/i><\/a> <b>1969<\/b>, <i>91<\/i>, 1194 (doi:10.1021\/ja01033a027).<\/li>\n<li>Dalton, D.R.; Liebman, S.A. &#8220;Thermal and Photolytic Decomposition of Diarylmethylenetriphenylphosphazines and Diaryldiazomethanes&#8221;,<a href=\"http:\/\/oxford.elsevier.com\/tis\">Tetrahedron<\/a><b> 1969 <\/b>,<i>25<\/i>, 3321 (doi:10.1016\/S0040-4020(01)82865-9).<\/li>\n<li>Hendrickson, J.B.; Alder, R.W.; Dalton, D.R.; Hey, D.G. &#8220;Some Approaches to Total Synthesis of Lycorine&#8221;,<a href=\"http:\/\/pubs.acs.org\/journals\/joceah\/index.html\"> <i>J. Org. Chem.<\/i> <\/a> <b>1969<\/b>, <i>34<\/i>, 2667 (doi:10.1021\/jo01261a040).<\/li>\n<li>Dalton, D.R.; Ramey, K.C.; Gisler, Jr., H.J.; Lendvay, L.J.; Abraham, A. &#8220;Hindered Rotation in Substituted 1,2,3,4-Tetrahydro-6,7-dimethyoxyisoquinolines&#8221;,<a href=\"http:\/\/pubs.acs.org\/journals\/jacsat\/index.html\"> <\/a><b>1969<\/b>, <i>91<\/i>, 6367 (doi: 10.1021\/ja01051a031.<\/li>\n<li>Charleston, B.S.; Dalton, C.K.; Washburne, S.S.; Dalton, D.R; Schraeder, S.R. &#8220;Chemistry of the Vinyl Cation &#8211; The Addition of DC1 to Allene&#8221;,<a href=\"http:\/\/oxford.elsevier.com\/tis\">Tetrahedron Lett.<\/a> <b>1969<\/b>, <i>10<\/i>, 5147 (doi:10.1016\/S0040-4039(01)88908-5).<\/li>\n<li>Dalton, D.R.;Smith, Jr., R.C.; Jones, D.G. &#8220;Bromoformate Formation in Dimethylformamide&#8221;, <a href=\"http:\/\/oxford.elsevier.com\/tis\">Tetrahedron<\/a><b> 1970<\/b>, <i>26<\/i>, 575 (doi:10.1016\/S0040-4020(01)97850-0).<\/li>\n<li>Dalton, D.R.; Liebman, S.A. &#8220;Electron Spin Resonance Studies on Neutral Hydrocarbon Radicals &#8211; Substituent and Isotope Effects&#8221;,<a href=\"http:\/\/oxford.elsevier.com\/tis\">Tetrahedron<\/a> <b>1970<\/b>, <i>26<\/i>, 3265 (doi:10.1016\/S0040-4020(01)92905-9).<\/li>\n<li>Dalton, D.R.; Dutta, V.P. &#8220;Bromohydrin Formation in Aqueous Dimethyl Sulphoxide; Electronic and Steric Effects&#8221;,<a href=\"http:\/\/www.rsc.org\/\"> <i>J. Chem. Soc. (B)<\/i><\/a> <b>1971<\/b>, 85 (doi:10.1039\/J29710000085).<\/li>\n<li>Dalton, D.R.; Miller, S.I.; Dalton, C.K.; J.K. Crelling, J.K.; &#8220;The Synthesis of Nitrobenzyl)-4-hydroxy-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline. Synthesis of 1-Substituted-4-oxygenated-1,2,3,4-tetrahydroisoquinolines&#8221;,<a href=\"http:\/\/oxford.elsevier.com\/tis\"> Tetrahedron Lett. <\/a><b> 1971<\/b>, <i>12<\/i>, 575 (doi:10.1016\/S0040-4039(01)96500-1).<\/li>\n<li>Dalton, D.R.; Rodebaugh, R.K.; Jefford, C.W. &#8220;Bromohydrin Formation in Dimethyl Sulfoxide. V. The Reaction of Norbornene&#8221;,<a href=\"http:\/\/pubs.acs.org\/journals\/joceah\/index.html\"> <i>J. Org. Chem.<\/i><\/a><b> 1972<\/b>,<i> 37<\/i>, 362 (doi:10.1021\/jo00968a006).<\/li>\n<li>Dalton, D.R.; Davis, R.M. &#8220;Bromohydrin Formation in Dimethyl Sulfoxide. The Reaction of Conjugated Dienes&#8221;,<a href=\"http:\/\/oxford.elsevier.com\/tis\">Tetrahedron Lett.<\/a> <b>1972<\/b>, <i>13<\/i>, 1057 (doi:10.1016\/S0040-4039(01)84507-X).<\/li>\n<li>Dalton, D.R.; Abraham, A.A. &#8220;The Synthesis of Aporphine Alkaloids III. Steric Effects in the Pschorr Cyclization&#8221;,<a href=\"http:\/\/www.rsc.org\/\"> <i> Synthetic Communications<\/i><\/a><b> 1972<\/b>, <i>2<\/i>, 303 (doi:10.1080\/00397917208061985).<\/li>\n<li>Dalton, D.R.; Foley, H.G.; Trueblood, K.N.; Murphy, M.R.. &#8220;Unusual Nitrones&#8221;<a href=\"http:\/\/oxford.elsevier.com\/tis\"> Tetrahedron Lett.<\/a><b> 1973<\/b>, <i>14<\/i>, 779 (doi:10.1016\/S0040-4039(01)95710-7).<\/li>\n<li>Liebman, S.A.;Dalton, D.R.;Knudsen, T.;Underwood, G. &#8220;Stereochemistry of the Diphenylmethyl Radical&#8221;, <i>J. Mag. Res.<\/i><b> 1973<\/b>,<i> 10<\/i>, 85 (doi:10.1016\/0022-2364(73)90238-2).<\/li>\n<li>Foley, H.G.; Dalton, D.R. &#8220;A Convenient, Neutral Conversion of Aldoximes to Nitriles at Low Temperature&#8221;,<a href=\"http:\/\/www.rsc.org\/is\/journals\/current\/chemcomm\/cccpub.htm\"> <i> Chemical Communications<\/i><\/a> <b>1973<\/b>,<i>17<\/i>, 628 (doi:10.1039\/C39730000628).<\/li>\n<li>Dalton, D.R.; Foley, H.G. &#8220;O-Carbamoyl Oximes&#8221;,<a href=\"http:\/\/pubs.acs.org\/journals\/joceah\/index.html\"> <i>J. Org. Chem.<\/i> <\/a><b> 1973<\/b>, <i>38<\/i>, 4200 (doi:10.1021\/jo00963a022).<\/li>\n<li>Foley, H.G.; Dalton, D.R. &#8220;A General, Neutral Beckmann Rearrangement of Ketoximes. The Isolation of an Intermediate&#8221;, <a href=\"http:\/\/www.rsc.org\/\"> <i> Synthetic Communications<\/i><\/a><b> 1974<\/b><i> 4<\/i>, 251 (doi:10.1080\/00397917408062082).<\/li>\n<li>Amar, F.; Dalton, D.R.; Eisman, G.; Haugh, M.J. &#8220;The Uncatalyzed Gas Phase Hydrochlorination of Alkenes I. Propene and Isobutylene&#8221;, <a href=\"http:\/\/oxford.elsevier.com\/tis\">Tetrahedron Lett.<\/a> <b>1974<\/b>, <i>15<\/i>, 3033 (doi:10.1016\/S0040-4039(01)91814-3).<\/li>\n<li>Amar, F.; Dalton, D.R.; Eisman, G.; Haugh, M.J. &#8220;The Uncatalyzed Gas Phase Hydrochlorination of Alkenes II. Allene&#8221;, <a href=\"http:\/\/oxford.elsevier.com\/tis\">Tetrahedron Lett.<\/a> <b>1974<\/b>,<i>15<\/i>, 3037 (doi:10.1016\/S0040-4039(01)91815-5).<\/li>\n<li>Haugh, M.J.; Dalton, D.R. &#8220;The Gas Phase Addition of Hydrogen Chloride to Propylene&#8221;, <a href=\"http:\/\/pubs.acs.org\/journals\/jacsat\/index.html\"> <i> J. Am. Chem. Soc.<\/i><\/a> <b>1975 <\/b>, <i>97<\/i>, 5674 (doi:10.1021\/ja00853a005).<\/li>\n<li>Krow, G.; Damodaran, M.; Michner, M.; Miller, S.I.; Dalton, D.R. &#8220;Nonsymmetric 9-Phenanthrylamines. An Improved Synthetic Procedure to a Useful Synthon&#8221;, <i>Synthetic Communications<\/i> <b>1976<\/b>, <i>6<\/i>, 261 (doi:10.1080\/00397917608063520).<\/li>\n<li>Scott, A.I.; Kang, J.; Dalton, D.R.; Chang, S.K. &#8220;Mechanism of Action of Coenzyme B12. An Overall Anionic Mechanism for Carbon-Skeleton Rearrangement in a Model Reaction&#8221;, <a href=\"http:\/\/pubs.acs.org\/journals\/jacsat\/index.html\"> <i>J. Am. Chem. Soc. <\/i><\/a> <b>1978<\/b>, <i>100<\/i>, 3603 (doi:10.1021\/ja00479a055).<\/li>\n<li>Langman, A.W.;Dalton, D.R. &#8220;Bromohydrins from Alkenes and N-Bromosuccinimide in Dimethyl Sulfoxide: erythro-2-Bromo-1,2-Diphenylethanol&#8221;,<a href=\"http:\/\/www.orgsyn.org\/Result.aspx?ga=na\"> <i>Organic Synthesis<\/i><\/a>  <b>1979<\/b> <i> 59<\/i> 16  (doi: 10.15227\/orgsyn.059.00160).<\/li>\n<li>Washburne, S.S.;Dalton, D.R. \u201cAn Analogy for Quantization of Energy Levels.\u201d <a href=\"https:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/ed057p200.3\"> <i>J. Chem. Educ.<\/i><\/a> <b>1980<\/b>, <i>57<\/i>, 200 (doi: 10.1021\/ed057p200.3).<\/li>\n<li> Chackalamannil, S.; Dalton, D.R. &#8220;The Synthesis of erythro and threo-N-methyl 7- Hydroxy-1,2,9,10-tetramethoxyaporphine&#8221;, <a href=\"http:\/\/oxford.elsevier.com\/tis\">Tetrahedron Lett.<\/a> <b>1980<\/b>, <i>21<\/i> 2029 (doi:10.1016\/S0040-4039(00)71477-8).<\/li>\n<li> Tierney, J.; Dalton, D.R. &#8220;A Homemade High Pressure Gas Cell&#8221;, <i>J. Chem. Educ.<\/i> <b>1981<\/b>, <i>58<\/i>, 813 (doi:10.1021\/ed058p813).<\/li>\n<li>Wert, K.L.; Chackalamannil, S.; Miller, E.; Dalton, D.R.; Zacharias, D.E.; Glusker, J.P. &#8220;Hoffmann Degradation of \u00e1-Hydroxy Ammonium Salts. <i>alpha-<\/i> and <i>beta-<\/i> Hydroxylaudanosine, 7-Hydroxyglaucine, and 13-Hydroxyxylopinine&#8221;,<a href=\"http:\/\/pubs.acs.org\/journals\/joceah\/index.html\"> <i> J. Org. Chem.<\/i><\/a> <b>1982<\/b>,<i> 47<\/i>, 5141 (doi:10.1021\/jo00147a020).<\/li>\n<li>Costello, F.; Dalton, D.R.; Poole, J.A. &#8220;Hydrochlorination of Alkenes. 2. Reactions of the Gases Hydrogen Chloride and 2-Methylpropene&#8221;, <i>J. Phys. Chem.<\/i><b> 1986<\/b>, <i>90<\/i>, 5352 (doi:10.1021\/j100412a091).<\/li>\n<li>Tierney, J.; Costello, F.; Dalton, D.R. &#8220;Hydrochlorination of Alkenes. 3. Reactions of the Gases Hydrogen Chloride and (<i>E<\/i>)- and (<i>Z<\/i>)-2-Butene&#8221;,<a href=\"http:\/\/pubs.acs.org\/journals\/joceah\/index.html\"> <i>J. Org. Chem. <\/i><\/a> <b>1986<\/b>, <i>51<\/i>, 5191 (doi:10.1021\/jo00376a026).<\/li>\n<li>Doshi, H.; Cardis, A.B.; Crelling, J.K.; Miller, S.I.; Dalton, D.R.; Zacharias, D.E.;  Glusker, J.P. &#8220;Hoffman Degradation of \u00e1-Hydroxy Ammonium Salts. II. 4-Hydroxybenzylisoquinolines and 4-Hydroxyaporphines&#8221;,<a href=\"http:\/\/pubs.acs.org\/journals\/joceah\/index.html\"> <i>J. Org. Chem.<\/i><\/a> <b>1987<\/b>, <i>52<\/i>, 2604 (doi:10.1021\/jo00388a053).<\/li>\n<li>Schnur, D.M.; Dalton, D.R. &#8220;MM2 Force Field Parameters for Oximes&#8221;, <a href=\"http:\/\/pubs.acs.org\/journals\/joceah\/index.html\"> <i>J. Org. Chem.<\/i><\/a> <b>1988<\/b>, <i>53<\/i>, 3313 (doi:10.1021\/jo00249a033).<\/li>\n<li>Schnur, D.M.; Yuh, Y.H.; Dalton, D.R. &#8220;A Molecular Mechanics Study of Amide Conformations,&#8221;<a href=\"http:\/\/pubs.acs.org\/journals\/joceah\/index.html\"> <i>J. Org. Chem.<\/i> <\/a> <b>1989<\/b>, <i>54<\/i>, 3779 (doi:10.1021\/jo00277a008).<\/li>\n<li>Eshraghi, J.; Longo, J.; Dalton D.R.; Harrington, G.W. &#8220;An Unusual Ring Contraction in the Formation of N-Nitrosohexamethyleneimine and N- Nitrosopiperidine from Tolazamide&#8221;, <i>Japanese J. Cancer Res. (Gann)<\/i> <b>1990<\/b>, <i>81<\/i>, 324 (doi:10.1111\/j.1349-7006.1990.tb02570.x).<\/li>\n<li>Mascavage, L.M.; Chi, H.; La S.; Dalton, D.R. &#8220;Surface-Catalyzed Hydrochlorination of Alkenes. The Reaction of the Gases Hydrogen Chloride and 1,3-Butadiene&#8221;,<a href=\"http:\/\/pubs.acs.org\/journals\/joceah\/index.html\"> <i>J. Org. Chem.<\/i><\/a> <b>1991<\/b>, <i>56<\/i>, 595 (doi:10.1021\/jo00002a021).<\/li>\n<li>Mascavage. L.M.; Dalton, D.R. &#8220;Surface Catalyzed Hydrochlorination of 1,3-Butadiene&#8221;, <a href=\"http:\/\/oxford.elsevier.com\/tis\">Tetrahedron Lett.<\/a> <b>1991<\/b>, <i>32<\/i>, 3461 (doi:10.1016\/0040-4039(91)80806-H).<\/li>\n<li>Kao, B.-C.; Doshi, H.; Reyes-Rivera, H.; Titus, D.D.; Yin, M.; Dalton, D.R.<br \/>\n&#8220;3-Substituted 2-Pyridinecarbaldoximes&#8221;, <i>J. Heterocyclic Chem.<\/i> <b>1991<\/b>, <i>28<\/i>, 1315 (doi:10.1002\/jhet.5570280525).<\/li>\n<li>Grant, A.D.; Zacharias, D.E.; Mascavage, L.M.; Kemmerer, G.E.; Dalton, D.R. &#8220;Chloromethylation of Codeine. Isolation of a Quaternary Iodide&#8221;, <i>J. Heterocyclic Chem.<\/i> <b>1993<\/b>, <i>30<\/i>, 553 (doi:10.1002\/jhet.5570300250).<\/li>\n<li>Jasmin, S.; Dalton, D.R.; Carroll P.J.; Kao, B.C. &#8220;The Synthesis and Spontaneous Resolution of 2-(3-Thioxothiazolidin-3-yl)thiazole.&#8221; <i>J. Heterocyclic Chem.<\/i> <b>1994<\/b> <i>31<\/i>, 1079 (doi:10.1002\/jhet.5570310464).<\/li>\n<li>Mascavage, L.M.; Zhang, F.; Dalton, D.R. &#8220;The Reaction of the Gases Hydrogen Chloride and 2-Butyne.&#8221; <a href=\"http:\/\/pubs.acs.org\/journals\/joceah\/index.html\"> <i>J. Org. Chem.<\/i><\/a> <b>1994<\/b>, <i>59<\/i>, 5048 (doi:10.1021\/jo00096a058).<\/li>\n<li>Reyes-Rivera, H.M.; Hutchins, R.O.; Dalton, D.R. &#8220;2-Carbaldoximes of Pyridine 4- and 5-Carboxylic Acids.&#8221; <a href=\"http:\/\/users.itsnet.com\/%7Ejhchem\/\">J. Heterocyclic Chem.<\/a> <b>1995<\/b>, <i>32<\/i>, 665 (doi:10.1002\/jhet.5570320248).<\/li>\n<li>Huang, Y.; Dalton D.R.; Carroll, P.J. &#8220;The Efficient, Enantio-selective Synthesis of Aza Sugars from Amino Acids. 1. The polyhydroxylated Pyrrolidines&#8221;.<a href=\"http:\/\/pubs.acs.org\/journals\/joceah\/index.html\"> <i> J. Org. Chem.<\/i> <\/a> <b>1997<\/b>,<i>62<\/i>, 372 (10.1021\/jo962028s).<\/li>\n<li>Huang, Y.; Sonnet, P.E.; Carroll, P.J.; Dalton, D.R. &#8220;Diastereoselective Diels-Alder Reactions. The Role of the Catalyst.&#8221;,<a href=\"http:\/\/oxford.elsevier.com\/tis\">Tetrahedron Lett.<\/a> <b> 2000 <\/b>, <i>41<\/i>, 2519   (doi:10.1016\/S0040-4039(00)00241-0).<\/li>\n<li>Mascavage, L.M.; Lu, Q.; Vey, J.; Dalton D.R.; Carroll, P.J. &#8220;Enantioselective Synthesis of Aza Sugars from Amino Acids. 2. The 3-Hydroxy-2-hydroxymethylpyrrolidines.&#8221;<a href=\"http:\/\/pubs.acs.org\/journals\/joceah\/index.html\"> <i> J. Org. Chem.<\/i> <\/a> <b>2001<\/b>,<i>66<\/i>, 3621 (doi:10.1021\/jo001736h).<\/li>\n<li>Huang, Y.; Sonnet, P.E.; Dalton, D.R. &#8220;Diasteroselective Diels-Alder Reactions. The Role of the Catalyst.2.&#8221; Archive for Organic Chemistry (ARKIVOC), <b> 2001 <\/b>: <i> Part (vi) <\/i> Commemorative Issue in Honor of Prof. Rudolph A. Abramovitch&#8230; <a href=\"http:\/\/www.arkat-usa.org\"> <i> ARKAT-USA <\/i> <\/a>:for the article itself, please click <a href=\"http:\/\/www.arkat-usa.org\/arkivoc-journal\/browse-arkivoc\/2001\/6\/\"> here <\/a> (doi:10.3998\/ark.5550190.0002.606).<\/li>\n<li>Wilson, M.L.; Dalton, D.R.; Carroll, P.J. &#8220;Decoration of the Aromatic Ring of Dihydrocodeinone (Hydrocodone) and 14-Hydroxydihydrocodeinone (Oxycodone)&#8221;. <a href=\"http:\/\/pubs.acs.org\/journals\/joceah\/index.html\"> <i> J. Org. Chem.<\/i> <\/a> <b>2005<\/b>, <i>70<\/i>, 6492 (10.1021\/jo050264+).<\/li>\n<li>Mascavage,L.M.; Wilson M.L.; Dalton, D.R. &#8221; Syntheses of Morphine and Codeine (1992 &#8211; 2002): Templates for Exploration of Synthetic Tools.&#8221;<a href=\"http:\/\/www.bentham.org\"> <i>Current Organic Synthesis<\/i> <\/a> <b> 2006 <\/b>, <i>3 <\/i> 99.<\/li>\n<li>Mascavage, L.M.; Sonnet P.E.; Dalton, D.R. &#8220;On the Surface-Catalyzed Reaction between the Gases 2,2-Dimethylpropanal and Methanamine. Formation of Active-Site Imines.&#8221; <a href=\"http:\/\/pubs.acs.org\/journals\/joceah\/index.html\"> <i> J. Org. Chem.<\/i> <\/a> <b>2006<\/b>, <i> 71 <\/i>, 3435 (doi:10.1021\/jo052503z).<\/li>\n<li>Sonnet, P.E.;  Mascavage L.M.; Dalton, D.R. &#8220;The First Steps. The Attack on the Carbonyl Carbon of Pyridoxal Cofactor in Pyridoxal- Dependent Enzymes.&#8221; <a href=\"http:\/\/www.elsevier.com\/locate\/bmcl\">,<i> Bioorg. Med. Chem. Lett. <\/i> <\/a> <b>2008<\/b>,<i>18<\/i>, 744 (doi:10.1016\/j.bmcl.2007.11.051).<\/li>\n<li>Mascavage, L.M.; Zhang-Plasket, F.; Sonnet, P.E.; Dalton, D.R. &#8220;Gas phase surface-catalyzed HCl addition to vinylacetylene: motion along a catalytic surface. Experiment and theory.&#8221; <a href=\"http:\/\/dx.doi.org\/10.1016\/j.tet.2008.07.081\"> <i> Tetrahedron <\/i> <\/a> <b> 2008 <\/b>, <i>64<\/i>, 9357 (doi:10.1016\/j.tet.2008.07.081) .<\/li>\n<li>Mascavage, L.M.; Tierney, J.;Sonnet, P.E.; Dalton, D.R. &#8220;The Hoffmann-Schiff dichotomy:on the reaction between chloral and amines&#8221; Archive for Organic Chemistry (ARKIVOC), <b> 2010 <\/b>: Commemorative Issue in Honor of Dr. Bruce E. Maryanoff and Dr. Cynthia A. Maryanoff <a href=\"http:\/\/www.arkat-usa.org\"> <i> ARKAT-USA <\/i> <\/a>: <b>2010<\/b> 278. For the article itself, please click <a href=\"http:\/\/www.arkat-usa.org\/arkivoc-journal\/browse-arkivoc\/2010\/8\/\"> here <\/a>(doi:10.3998\/ark.5550190.0011.819).<\/li>\n<li>Judge, E.J.; Brady, J.J.; Dalton. D.R.; Levis, R.J. &#8220;Analysis of Pharmaceutical Compounds from Glass, Fabric, Steel, and Wood Surfaces at Atmospheric Pressure Using Spatially Resolved Nonresonant Femtosecond Laser Vaporization Electrospray Mass Spectrometry&#8221; <a href=\"http:\/\/pubs.acs.org\/journal\/ancham\"> <i>Anal. Chem. <\/i> <\/a>: <b> 2010 <\/b>, <i> 82 <\/i>, 3231 (doi:10.1021\/ac902880q).<\/li>\n<li> Mascavage, L.M.; Sonnet, P.E.; Dalton, D.R. &#8220;Surface-Catalyzed Reaction between the Gases Hydrogen Chloride and Isoprene&#8221; <a href=\"http:\/\/pubs.acs.org\/journal\/aesccq\"> <i> ACS Earth Space Chem. <\/i> <\/a> <b>2017 <\/b> <i> 3 <\/i>, 122 (doi:10.1021\/acsearthspacechem.7b00009).<\/li>\n<p><b>PATENTS <\/b><\/p>\n<hr>\n<ul>\n<li>D. R. Dalton, Y. Huang, &#8220;Process of the Enantioselective Synthesis of Hydroxypyrrolidines from Amino Acids&#8221; U.S. #5,801,247, assigned to Temple University &#8211; of the Commonwealth System of Higher Education (<b>1998<\/b>).<\/li>\n<li>E. S. Blake, R. E. DeBrunner, and D. R. Dalton, &#8220;Fluorine Containing Phosphoramidates,&#8221; U.S. #3,558,748, assigned to the Monsanto Company (<b>1971<\/b>).<\/li>\n<li>E. S. Blake, R. E. DeBrunner, and D. R. Dalton, &#8220;Fluorine Containing Organophosphorus Compounds,&#8221; U.S. #3,346,647, assigned to the Monsanto Company (<b>1967<\/b>).<\/li>\n<li>E. S. Blake, D. R. Dalton, and R. E. DeBrunner, &#8220;Fluorine Containing Organic Compounds of Phosphorus,&#8221; U.S. #3,288,890, assigned to the Monsanto Company (<b>1966<\/b>).<\/li>\n<\/ul>\n<hr>\n<p>OTHER <b> REFEREED <\/b> WORKS PUBLISHED OR IN PRESS:<\/p>\n<hr>\n<ul>\n<li>Alkaloids:, <i>Kirk-Othmer Encyclopedia of Chemical Technology<\/i>, 4th Edition, <a href=\"http:\/\/http:\/\/www.mrw.interscience.wiley.com\/kirk\/\"> Wiley,<\/a>, New York, <b>1991<\/b>. Vol. 1, pp 1039-1087.<\/li>\n<li>&#8220;Halogen Hydride Addition to Alkenes and Alkynes&#8221;, <i>Trends in Organic Chemistry<\/i>, <b>1993<\/b>, <i>4<\/i>, 303-333. Council of Scientific Research Integration, ed. Trivandrum, INDIA<\/li>\n<li>&#8220;Copper(I) iodide-Potassium naphthalenide&#8221;, <i>Encyclopedia of Reagents for Organic Synthesis<\/i>, <a href=\"http:\/\/www3.interscience.wiley.com\/\">Wiley<\/a>, New York, <b>1995<\/b>, <i>2<\/i>, 1350.<\/li>\n<li>&#8220;Copper(I) iodide-tributylphosphine&#8221;, <i>Encyclopedia of Reagents for Organic Synthesis<\/i>, <a href=\"http:\/\/www3.interscience.wiley.com\/\">Wiley<\/a> , New York, <b>1995<\/b>, <i>2<\/i>, 1351.<\/li>\n<li>&#8220;Copper(I) iodide-tributylphosphite&#8221;, <i>Encyclopedia of Reagents for Organic Synthesis<\/i>, <a href=\"http:\/\/www3.interscience.wiley.com\/\">Wiley<\/a> , New York, <b>1995<\/b>, <i>2<\/i>, 1353.<\/li>\n<li>&#8220;Copper(I) iodide-triethylphosphite&#8221;, <i>Encyclopedia of Reagents for Organic Synthesis<\/i>, <a href=\"http:\/\/www3.interscience.wiley.com\/\">Wiley<\/a>, New York, <b>1995<\/b>, <i>2<\/i>, 1354.<\/li>\n<li>&#8220;Copper(I) iodide-trimethylphosphite&#8221;, <i>Encyclopedia of Reagents for Organic Synthesis<\/i>, <a href=\"http:\/\/www3.interscience.wiley.com\/\">Wiley<\/a>, New York, <b>1995<\/b>, <i>2<\/i>, 1355.<\/li>\n<li>&#8220;Copper(I) iodide-triethylphosphine-Lithium naphthalenide&#8221;,<i> Encyclopedia of Reagents for Organic Synthesis<\/i>,<a href=\"http:\/\/www3.interscience.wiley.com\/\">Wiley<\/a> , New York, <b>1995<\/b>, <i>2<\/i>, 1354.<\/li>\n<li><b>Alkaloids<\/b>:, <i>Kirk-Othmer <b>Condensed <\/b> Encyclopedia of Chemical Technology<\/i>, 4th Ed.<a href=\"http:\/\/www.mrw.interscience.wiley.com\/kirk\/\"> Wiley,<\/a> New York, <b>1999<\/b><\/li>\n<li>Report: &#8220;Strychnine Alkaloids&#8221; <i>Encyclopedia of Science and Technology<\/i>, Ninth Edition, Vol 17. <a href=\"http:\/\/www.mhest.com\"> McGraw-Hill Book Co.<\/a>, New York, <b>2003<\/b>.<\/li>\n<li><b>Alkaloids<\/b>:, <i>Kirk-Othmer Encyclopedia of Chemical Technology<\/i>, On-line Edition, <a href=\"http:\/\/www.mrw.interscience.wiley.com\/kirk\/\"> Wiley,<\/a>, New York, <b>2003<\/b>.<\/li>\n<li><b>Alkaloids <\/b>:, <i>Kirk-Othmer Encyclopedia of Chemical Technology<\/i>, 5th Edition, <a href=\"http:\/\/www.mrw.interscience.wiley.com\/kirk\/\"> Wiley,<\/a>, New York, <b>2004<\/b>. Vol. 2, pp 71-113.<\/li>\n<li><b>Alkaloids<\/b> Mascavage, L. M.; Jasmin, S. ; Sonnet, P. E.; Wilson, M.; Dalton, D. R. &#8220;Alkaloids&#8221; in <i> Ullmann&#8217;s Encyclopedia of Industrial Technology<\/i>, <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/14356007.a01_353.pub2\/otherversions\"> Wiley, <\/a>, DOI:10.1002\/14356007.a01_353.pub2, <b><b> 2011.<\/b><\/b><br \/>\n<hr>\n<\/li>\n<li><b><b>Book Review: <\/b><\/b>&#8220;The Molecules of Nature&#8221; by J. B. Hendrickson, <i>Rec. Chem. Progress <\/i><strong>1966<\/strong>, <i>27<\/i>, 199.<\/li>\n<li><b><b>Report: <\/b><\/b>&#8220;Gas Phase NMR Spectra&#8221; TAMU Newsletter <strong>1981<\/strong>, 278-11.<\/li>\n<li><b><b>Book Review: <\/b><\/b>&#8220;The Alkaloids&#8221; by M. F. Grundon, <i>J. Am. Chem. Soc.<\/i> <strong>1983<\/strong>, <i>105<\/i>, 5717.<\/li>\n<li><b><b>Computer Software Review: &#8220;<\/b><\/b>Molecular Graphics&#8221; by B. H. Robinson, <i>J. Am. Chem. Soc. <\/i><strong>1987<\/strong>, <i>109<\/i>, 2862.<\/li>\n<li><b>Preprint <strong>2025<\/strong>&#8211; Not peer reviewed<\/b>: &#8220;Growing Grapes in the Time of Dramatic Climate Change&#8221; https:\/\/www.preprints.org\/manuscript\/202501.2081\/v1<\/li>\n<\/li>\n<\/ul>\n<hr>\n<p><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><i><\/i><\/ul>\n","protected":false},"excerpt":{"rendered":"<p>David Robert Dalton EDUCATION and POSITIONS HELD: Northwestern University, Evanston, IL, B.A. (with Honors), 1957. University of California, Los Angeles, CA, Ph.D., 1962. 1962-1964 Research Chemist, Monsanto Research Corporation Dayton Laboratories. A division of the Monsanto Company (acquired by Bayer in 2018). 1964-1965 Instructor and National Institutes of Health, Postdoctoral Fellow, The Ohio State University, [&hellip;]<\/p>\n","protected":false},"author":621,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"open","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-12","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/sites.temple.edu\/daltongroup\/wp-json\/wp\/v2\/pages\/12","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/sites.temple.edu\/daltongroup\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/sites.temple.edu\/daltongroup\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/sites.temple.edu\/daltongroup\/wp-json\/wp\/v2\/users\/621"}],"replies":[{"embeddable":true,"href":"https:\/\/sites.temple.edu\/daltongroup\/wp-json\/wp\/v2\/comments?post=12"}],"version-history":[{"count":8,"href":"https:\/\/sites.temple.edu\/daltongroup\/wp-json\/wp\/v2\/pages\/12\/revisions"}],"predecessor-version":[{"id":190,"href":"https:\/\/sites.temple.edu\/daltongroup\/wp-json\/wp\/v2\/pages\/12\/revisions\/190"}],"wp:attachment":[{"href":"https:\/\/sites.temple.edu\/daltongroup\/wp-json\/wp\/v2\/media?parent=12"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}