{"id":19,"date":"2016-10-07T17:49:35","date_gmt":"2016-10-07T17:49:35","guid":{"rendered":"https:\/\/scholarblogs.emory.edu\/padwalab\/?page_id=19"},"modified":"2018-06-28T19:28:22","modified_gmt":"2018-06-28T19:28:22","slug":"recent-publications","status":"publish","type":"page","link":"https:\/\/scholarblogs.emory.edu\/padwalab\/recent-publications\/","title":{"rendered":"Recent Publications"},"content":{"rendered":"
    \n
  1. \u201cGeneral Access to the Vinca and Tacaman Alkaloids Using a Rh(II)-Catalyzed Cyclization\/Cycloaddition Cascade ; A. Padwa and D. England J. Org. Chem. 73<\/b><\/span>, 2792 (2008).<\/li>\n
  2. \u201cA Rh(II)-Catalyzed Cycloaddition Approach Toward the Synthesis of Komaroviquinone ; A. Padwa and D. England Tetrahedron 64<\/b><\/span>, 4758 (2008).<\/li>\n
  3. \u201cUtilization of a Michael Addition: Dipolar Cycloaddition Cascade for the Synthesis of Cylindricine C ; A. Padwa, A. Flick and M. J. A. Caballero Organic Letters 10<\/b><\/span>, 1871 (2008).<\/li>\n
  4. \u201cA General Synthetic Entry to the Pentacyclic Strychnos Alkaloid Family Using a [4+2]-Cycloaddition\/Rearrangement Cascade Sequence ; A. Padwa, J. Boonsombat, H. Zhang, M. J. Chughtai, and J. Hartung, Jr. J. Org. Chem. 73<\/b><\/span>, 3539 (2008).<\/li>\n
  5. \u201cGold-Catalyzed Intramolecular Cycloisomerization of Indolo Substituted Propargyl-carboxamides: Application Towards the Synthesis of Lavendamycin Analogues ; A.Padwa and D. England Organic Letters 10<\/b><\/span>, 3631 (2008).<\/li>\n
  6. \u201cA New Route to Heterocyclic Compounds by the Mercuric Acetate Oxidation of N-Alkyl Substituted 4-Piperidones ; A. Padwa and A. C. Flick Tetrahedron Letters 49<\/b><\/span>, 5739 (2008).<\/li>\n
  7. \u201cGold- and Silver-Mediated Cycloisomerizations of N-Propargylamides ; G. Verniest and A. Padwa Organic Letters 10<\/b><\/span>, 4379 (2008).<\/li>\n
  8. \u201cCycloaddition Across the Benzofuran Ring as an Approach to the Morphine Alkaloids ; S. France, J. Boonsombat, C. Leverett and A. Padwa J. Org. Chem. 73<\/b><\/span>, 8120 (2008).<\/li>\n
  9. \u201cA Stereoselective Approach to the Azaspiro[5.5]undecane Ring System Using a Conjugate Addition\/Dipolar Cycloaddition Cascade: Application to the Total Synthesis of 2,7,8-epi-Perhydrohistrionicotoxin ; A. Padwa and M. Wilson J. Org. Chem. 73<\/b><\/span>, 9601 (2008).<\/li>\n
  10. \u201cThe Rhodium(II) Carbenoid Cyclization-Cycloaddition Cascade of alpha-Diazo Dihydro-indolinones for the Synthesis of Novel Azapolycyclic Ring Systems ; A. Padwa, D. B. England, J. M. Eagan, G.Merey, and O. Anac Tetrahedron 64<\/b><\/span>, 988 (2008).<\/li>\n
  11. \u201cSynthesis of 2,4-Disubstituted Pyrroles by Rearrangements of 2-Furanyl Carbamates ; A. Padwa, S. Kiren, X. Hong, and C. A. Leverett Organic Letters 11<\/b><\/span>, 1233 (2009).<\/li>\n
  12. \u201cConjugate Addition-Dipolar Cycloaddition Cascade for the Synthesis of Benzo[a]quinolizine and Indolo[a]quinolizine Scaffolds: Application for the Total Synthesis of Yohimbenone ; A. Padwa, C. J. Stearman and M. Wilson J. Org. Chem. 74<\/b><\/span>, 3491 (2009).<\/li>\n
  13. \u201cCycloaddition Studies Directed Toward the Srychnos Alkaloid Min\u00ef\u00ac\u0081ensine ; A. Padwa, D. R. Bobeck, S. France, C. A. Leverett, and F. Sanchez-Cantalej Tetrahedron Lett. 50<\/b><\/span>, 3145 (2009).<\/li>\n
  14. \u201cA Chemistry Cascade: From Physical Organic Studies of Alkoxy Radicals to Alkaloid Synthesis ; A. Padwa J. Org. Chem. 74<\/b><\/span>, 6421 (2009).<\/li>\n
  15. \u201cA Facile Synthesis of 5-Alkoxypyrrol-2(5H)-ones Using a Modified Aza-Achmatowicz Oxidation ; S. Kiren, X. Hong, C. A. Leverettt, and A. Padwa Tetrahedron 65<\/b><\/span>, 6720 (2009).<\/li>\n
  16. \u201cApplication of Cross Conjugated Heteroaromatic Betaines Toward the Synthesis of the Schizozygane Alkaloid Strempeliopine ; A. Padwa, C. A. Leverett and X. Hong Acta Chim. Slov 56<\/b><\/span>, 527 (2009).<\/li>\n
  17. \u201cTotal Synthesis of the Alkaloid Aspidophytine Based on Carbonyl Ylide Cycloaddition Chemistry ; D. R. Bobeck, H. Lee, A. C. Flick, and A. Padwa J. Org. Chem. 74<\/b><\/span>, 7389 (2009).<\/li>\n
  18. \u201cHeteroaryl Cross-Coupling as an Entry toward the Synthesis of Lavendamycin Analogues: A Model Study ; A. Padwa, G. Verniest, X. Wang and N. De Kimpe J. Org. Chem. 75<\/b><\/span>, 424 (2010).<\/li>\n
  19. \u201cSynthesis of Substituted beta-Carbolines via Gold(III)-Catalyzed Cycloisomerization of N-Propargylamides ; G. Verniest, D. England, N. De Kimpe and A. Padwa Tetrahedron 66<\/b><\/span>, 1496 (2010).<\/li>\n
  20. \u201c2,3-Bis(phenylsulfonyl)-1,3-butadiene as a Reagent for the Synthesis of the Azatricyclic Core of Halichlorine ; A. C. Flick, M. J. A. Caballero, H. Ik Lee, and A. Padwa J. Org. Chem. 75<\/b><\/span>, 1992 (2010).<\/li>\n
  21. \u201cA Conjugate Addition\/Dipolar-Cycloaddition Cascade Sequence for the Synthesis of Cylindricine ; A. C. Flick, M. J. A. Caballero, A. Padwa Tetrahedron 66<\/b><\/span>, 3643 (2010).<\/li>\n
  22. \u201cIntramolecular [4+2]-Cycloaddition of 5-Amino-Substituted Oxazoles as an Approach toward the Left-Hand Segment of Haplophytine ; M. Chughtai, J. M. Eagan, and A. Padwa Synlett 21<\/b><\/span>, 215 (2011).<\/li>\n
  23. \u201cSynthesis of N-vinyl substituted indoles and their acid-catalyzed behavior ; H. Li, N. Boonnak, A. Padwa Tetrahedron Lett. 52<\/b><\/span>, 2062 (2011).<\/li>\n
  24. \u201cAn IMDAF Cycloaddition Approach toward the Synthesis of the Lycopodium Alkaloid Fawcettidine ; J. Boonsompat and A.Padwa J. Org. Chem 76<\/b><\/span>, 2753 (2011).<\/li>\n
  25. \u201cIntramolecular Diels-Alder Cycloaddition\/Rearrangement Cascade of an Amidofuran Derivative for the Synthesis of Minfiensine ; G. Li and A. Padwa Organic Letters 13<\/b><\/span>, 3767 (2011).<\/li>\n
  26. \u201cIntramolecular Cycloaddition of Carbonyl Ylides as a Strategy for Natural Product Synthesis ; A. Padwa Tetrahedron 67<\/b><\/span>, 8057 (2011).<\/li>\n
  27. \u201cAn Approach Toward The Alkaloid Mersicarpine Using a Rhodium(II) Carbenoid Cyclization\u00e2\u20ac\u201cCycloaddition Cascade of an alpha-Diazo Dihydroindolinone ; H. Li, B. Cheng, N. Boonnak, and A. Padwa Tetrahedron 67<\/b><\/span>, 9829 (2011).<\/li>\n
  28. \u201cN-Alkenyl Indoles as Useful Intermediates for Alkaloid Synthesis ; H. Li, N. Boonnak and A. Padwa J. Org. Chem. 76<\/b><\/span>, 9488 (2011).<\/li>\n
  29. \u201c2,3-Bis(phenylsulfonyl)-1,3-butadiene as a Reagent for the Synthesis of Azapolycylic Ring Systems ; A. C. Flick and A. Padwa J. Sulfur Chemistry 34<\/b><\/span>, 7 (2013).<\/li>\n
  30. \u201c2,3-Bis(phenylsulfonyl)-1,3-butadiene as a Reagent for the Synthesis of Piperidone Derivatives ; A. C. Flick and A. Padwa J. Sulfur Chemistry 34<\/b><\/span>, 88 (2013).<\/li>\n
  31. \u201cUse of Sulfur Fragments for the Synthesis of Nitrogen Heterocycles ; A. Padwa Pure Appl. Chem 85<\/b><\/span>, 701 (2013).<\/li>\n
  32. \u201cRh(II)-Catalyzed Reactions of Differentially 2-Substituted Bis(diazo) Functionalities ; S. A. Bonderoff and A. Padwa Organic Letters 15<\/b><\/span>, 4114 (2013).<\/li>\n
  33. \u201cNatural Product Synthesis via the Rhodium Carbenoid Mediated Cyclization of Diazo Carbonyl Compounds ; A. Padwa, B. Cheng and Y. Zou Aust. J. Chem 67<\/b><\/span>, 343 (2014).<\/li>\n
  34. \u201cModel Studies Directed Toward the Alkaloid Mersicarpine Utilizing a Rh(II)-Catalyzed Insertion\/Cycloaddition Sequence ; H. Li, S. Bonderoff, B. Cheng and A. Padwa J. Org. Chem. 79<\/b><\/span>, 392 (2014).<\/li>\n
  35. \u201cIntramolecular Cycloaddition Reactions of Furo[3,4-b]indoles for Alkaloid Synthesis ; Y. Zou, B. Cheng, H. Li, N. Downer-Riley and C. Straub J. Org. Chem. 79<\/b><\/span>, 3173 (2014).<\/li>\n
  36. \u201cRhodium(II) Catalyzed Cyclopropanation\/Cycloaddition Reactions of the Bis(diazo)-piperidin-2- one System ; S. A. Bonderoff and A. Padwa Tetrahedron Letters 76<\/b><\/span>, 9488 (2011).<\/li>\n
  37. \u201cSolvent and Ligand Effects Associated with the Rh(II)-Catalyzed Reaction of Diazo Substituted Amido Esters ; A. Padwa and Y. Zou J. Org. Chem. 80<\/b><\/span>, 1802 (2015).<\/li>\n
  38. \u201cIMDAF Cascade Approach toward the Synthesis of the Alkaloid (\u00b1)-Minfiensine\u201d C. A. Leverett, G. Li, S. France and A. Padwa J. Org. Chem. <\/strong>81<\/em>, 10193 (2016).<\/li>\n
  39. \u201cPolycyclic Ring Formation Using Bis-diazolactams for Cascade Stitching\u201d S. A. Bonderoff and A. Padwa J. Org. Chem. <\/strong>82<\/em>, 642 (2017).<\/li>\n<\/ol>\n

    Reviews & Book Chapters<\/h2>\n
      \n
    1. \u201cCycloaddition Methodology: A Useful Entry Towards Biologically Active Heterocycles; U. Chiacchio, A. Padwa and G. Romeo, Current Organic Chemistry, 13, <\/b><\/span> pp 422-447 (2009).<\/li>\n
    2. \u201cDomino Reactions of Rhodium(II) Carbenoids for Alkaloid Synthesis; U. Chiacchio, A. Padwa and G. Romeo, Chem. Soc. Rev., 38, <\/b><\/span> pp 3072-3095 (2009).<\/li>\n
    3. \u201cCascade Reactions of Carbonyl Ylides for Heterocyclic Synthesis ; A. Padwa, Progress in Heterocyclic Chemistry, Chapter 2, G. W. Gribble and J. A. Joule, eds, Elsevier, Vol 20<\/b><\/span>, pp 20-46 (2009).<\/li>\n
    4. \u201cAziridines and Azirines, Monocyclic ; A. Padwa in Comprehensive Heterocyclic Chemistry, Vol III, A. R. Katritzky, Ed., Elsevier, Vol 18<\/b><\/span>, pp 1-97 (2008).<\/li>\n
    5. \u201cThree Membered Ring Systems ; A. Padwa and S. S. Murphree, Progress in Heterocyclic Chemistry, Chapter 3.1, G. W. Gribble and J. A. Joule eds, Pergamon Press, Vol 18<\/b><\/span>, pp 55-80 (2007).<\/li>\n
    6. \u201cThe Synthesis of Heterocycles Using Cascade Chemistry; Advances in Heterocyclic Chemistry, Elsevier; Katritzky, A., Ed., Vol 94<\/b><\/span>, 2007, pp 1-105<\/li>\n
    7. \u201cUtilization of 1,2-Thioalkyl Shifts for Alkaloid Synthesis; A. Padwa Phosphorus, Sulfur, and Silicon, and the Related Elements 180<\/b><\/span>, p 1149 (2005)<\/li>\n
    8. \u201cHighly Stereoselective Vinylogous Pummerer Rearrangement; J. L. G. Ruano, J. Alem\u00c2\u2021n, M. T. Aranda, M. J. Ar\u00c2\u017dvalo, and A. Padwa, Phosphorus, Sulfur, and Silicon, and the Related Elements 180<\/b><\/span>, p 1497 (2005)<\/li>\n
    9. \u201cThree Membered Ring Systems\u201d A. Padwa and S. S. Murphree, Progress in Heterocyclic Chemistry<\/b><\/span>, Chapter 3, G. W. Gribble and J. A. Joule, eds, Pergamon Press, Vol 16, pp 54-81 (2004)<\/li>\n
    10. \u201cHeteroatom Analogues of Aldehydes and Ketones: An Introduction; A. Padwa Science of Synthesis, Vol 27<\/b><\/span>, A. Padwa, Ed., G. Thieme Verlag, Stuttgart, Germany, pp 1-20 (2004)<\/li>\n
    11. \u201cThe Pummerer Reaction: Methodology and Strategy for the Synthesis of Heterocyclic Compounds; A. Padwa and S. Bur, Chem. Reviews 104<\/b><\/span>, 2401 (2004)<\/li>\n
    12. \u201cCycloaddition and Cyclization Chemistry of 2H-Azirines; A. Padwa Advances in Heterocyclic Chemistry 99<\/b><\/span>, 1 (2010)<\/li>\n
    13. \u201cAmmonium Ylides as Building Blocks for Alkaloid Synthesis; S. Bur and A. Padwa Modern Tools for the Synthesis of Complex Bioactive Molecules, John Wiley<\/b><\/span>, 455 (2012)<\/li>\n
    14. \u201cIntramolecular Diels-Alder Cycloaddition of Furans (IMDAF) for Natural Product Synthesis; A. Padwa and A. C. Flick Advances in Heterocyclic Chemistry 110<\/b><\/span>, 1 (2013)<\/li>\n
    15. \u201c[4+2]-Cycloaddition Chemistry of Substituted Furans\u201d A. Padwa Methods and Applications of Cycloaddition Reactions in Organic Syntheses, John Wiley <\/b><\/span>, 355 (2014)<\/li>\n
    16. \u201cRecent Advances of 1,3-Dipolar Cycloaddition Chemistry for Alkaloid Synthesis\u00e2\u20ac\u009d, \u201d A. Padwa Advances in Heterocyclic Chemistry Vol 119, Elsevier<\/b><\/span>, 241 (2016)<\/li>\n
    17. \u201cAsymmetric Reactions Employing 1,3-Dipoles\u201d A. Padwa and S. Bur Chem. Heterocycl. Compd. Vol 52<\/b><\/span>, (2016)<\/li>\n
    18. \u201cCycloaddition Chemistry of Carbonyl Ylides for Alkaloid Synthesis\u201d A. Padwa Russ. Chem. Bull. (Int. Ed.) Vol 65 <\/b><\/span>, 2183 (2016)<\/li>\n
    19. \u201cUse of Rhodium Carbenoid Intermediates for Dipolar Cycloaddition Chemistry\u201d A. Padwa, Progress in Heterocyclic Chemistry<\/strong>, Chapter 2, G. W. Gribble and J. A. Joule, eds, Elsevier Science, Vol 29, pp 45-64 (2017).<\/li>\n
    20. \u201cUse of Nitrogen and Oxygen Dipole Ylides for Alkaloid Synthesis. A. Padwa (GG-10416UR) ARKIVOC e-Journal<\/strong> Vol. 20, Part IV, DOI:\u00a0https:\/\/doi.org\/10.24820\/ark.5550190.p010.416<\/a>, pp 23-49, 2018<\/strong>.<\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"

      \u201cGeneral Access to the Vinca and Tacaman Alkaloids Using a Rh(II)-Catalyzed Cyclization\/Cycloaddition Cascade ; A. Padwa and D. England J. Org. Chem. 73, 2792 (2008). \u201cA Rh(II)-Catalyzed Cycloaddition Approach Toward the Synthesis of Komaroviquinone ; A. Padwa and D. England Tetrahedron 64, 4758 (2008). \u201cUtilization of a Michael Addition: Dipolar Cycloaddition Cascade for the Synthesis […]<\/p>\n","protected":false},"author":2946,"featured_media":0,"parent":0,"menu_order":3,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-19","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/scholarblogs.emory.edu\/padwalab\/wp-json\/wp\/v2\/pages\/19","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/scholarblogs.emory.edu\/padwalab\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/scholarblogs.emory.edu\/padwalab\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/scholarblogs.emory.edu\/padwalab\/wp-json\/wp\/v2\/users\/2946"}],"replies":[{"embeddable":true,"href":"https:\/\/scholarblogs.emory.edu\/padwalab\/wp-json\/wp\/v2\/comments?post=19"}],"version-history":[{"count":6,"href":"https:\/\/scholarblogs.emory.edu\/padwalab\/wp-json\/wp\/v2\/pages\/19\/revisions"}],"predecessor-version":[{"id":136,"href":"https:\/\/scholarblogs.emory.edu\/padwalab\/wp-json\/wp\/v2\/pages\/19\/revisions\/136"}],"wp:attachment":[{"href":"https:\/\/scholarblogs.emory.edu\/padwalab\/wp-json\/wp\/v2\/media?parent=19"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}