{"id":11,"date":"2015-05-07T08:56:42","date_gmt":"2015-05-07T12:56:42","guid":{"rendered":"http:\/\/umaine.edu\/brichlab\/?page_id=11"},"modified":"2021-09-16T21:10:35","modified_gmt":"2021-09-17T01:10:35","slug":"research","status":"publish","type":"page","link":"https:\/\/umaine.edu\/brichlab\/research\/","title":{"rendered":"Publications"},"content":{"rendered":"<h2>Publications:<\/h2>\n<p>17. <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2021\/ob\/d1ob00941a\">T. Cheewawisuttichai, M. Brichacek \u201cDevelopment of a multifunctional neoglycoside auxiliary for applications in glycomics research\u201d <em>Org. Biomol. Chem.<\/em> <strong>2021<\/strong>, <em>19<\/em>, 6613-6617.<\/a><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-272 size-full\" src=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/Tetrazine-neoglycoside-glycan-auxiliary.gif\" alt=\"Tetrazine neoglycoside glycan auxiliary\" width=\"378\" height=\"124\" \/><\/p>\n<p>16. \u00a0<a href=\"https:\/\/www.mdpi.com\/1420-3049\/26\/12\/3661\">A. Numan, M. Brichacek \u201cAsymmetric Synthesis of Stereogenic Phosphorus P(V) Centers Using Chiral Nucleophilic Catalysis\u201d <em>Molecules<\/em><strong> 2021<\/strong>, <em>26<\/em> (12), 3661.<\/a><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-271 size-large\" src=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/Oxidative-substitution-of-phosphonates-with-asymmetric-catalysts-e1631840834469-1024x174.png\" alt=\"Oxidative substitution of phosphonates with asymmetric catalysts\" width=\"1024\" height=\"174\" srcset=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/Oxidative-substitution-of-phosphonates-with-asymmetric-catalysts-e1631840834469-1024x174.png 1024w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/Oxidative-substitution-of-phosphonates-with-asymmetric-catalysts-e1631840834469-300x51.png 300w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/Oxidative-substitution-of-phosphonates-with-asymmetric-catalysts-e1631840834469-768x131.png 768w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/Oxidative-substitution-of-phosphonates-with-asymmetric-catalysts-e1631840834469-1536x261.png 1536w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/Oxidative-substitution-of-phosphonates-with-asymmetric-catalysts-e1631840834469-2048x348.png 2048w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/Oxidative-substitution-of-phosphonates-with-asymmetric-catalysts-e1631840834469-105x18.png 105w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/Oxidative-substitution-of-phosphonates-with-asymmetric-catalysts-e1631840834469-317x54.png 317w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/Oxidative-substitution-of-phosphonates-with-asymmetric-catalysts-e1631840834469-423x72.png 423w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/Oxidative-substitution-of-phosphonates-with-asymmetric-catalysts-e1631840834469-634x108.png 634w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/Oxidative-substitution-of-phosphonates-with-asymmetric-catalysts-e1631840834469-846x144.png 846w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/Oxidative-substitution-of-phosphonates-with-asymmetric-catalysts-e1631840834469-951x162.png 951w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/Oxidative-substitution-of-phosphonates-with-asymmetric-catalysts-e1631840834469-1268x216.png 1268w\" sizes=\"auto, (max-width: 320px) 85vw, (max-width: 768px) 67vw, (max-width: 1024px) 62vw,1024px\" \/><\/p>\n<p>15. <a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0008621521000513\">T. Cheewawisuttichai, R. D. Hurst,\u00a0 M. Brichacek \u201cTransformation of aldehydes into nitriles in an aqueous medium using O-phenylhydroxylamine as the nitrogen source\u201d <em>Carbohydate Res.<\/em> <strong>2021<\/strong>, <em>502<\/em>, Epub 108282.<\/a><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-270 size-full\" src=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/O-Phenylhydroxylamine-conversion-of-aldehyde-to-cyanohydrin.jpg\" alt=\"O Phenylhydroxylamine conversion of aldehyde to cyanohydrin\" width=\"500\" height=\"160\" srcset=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/O-Phenylhydroxylamine-conversion-of-aldehyde-to-cyanohydrin.jpg 500w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/O-Phenylhydroxylamine-conversion-of-aldehyde-to-cyanohydrin-300x96.jpg 300w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/O-Phenylhydroxylamine-conversion-of-aldehyde-to-cyanohydrin-105x34.jpg 105w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/O-Phenylhydroxylamine-conversion-of-aldehyde-to-cyanohydrin-317x101.jpg 317w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/O-Phenylhydroxylamine-conversion-of-aldehyde-to-cyanohydrin-423x135.jpg 423w\" sizes=\"auto, (max-width: 320px) 85vw, (max-width: 768px) 67vw, (max-width: 1024px) 62vw,500px\" \/><\/p>\n<p>14. <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2019\/dt\/c9dt01823a\">E. N. Patel, R. B. Arthur, A. D. Nicholas, E. W. Reinheimer, M. A. Omary,M. Brichacek*<strong><sub>, <\/sub><\/strong>H. H. Patterson* \u201cSynthesis, structure and photophysical properties of a 2D network with gold dicyanide donors coordinated to aza[5]helicene viologen acceptors\u201d <em>Dalton Trans. <\/em><strong>2019<\/strong>, <em>48<\/em>, 10288-10297.<\/a><\/p>\n<figure id=\"268\" class=\"wp-caption aligncenter\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-268 size-full\" src=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/Aza5-helicene-viologen.gif\" alt=\"Aza5 helicene viologen \" width=\"348\" height=\"189\" \/><figcaption class=\"wp-caption-text\">Aza5 helicene viologen<\/figcaption><\/figure>\n<p><a href=\"https:\/\/www.nature.com\/articles\/s41598-019-39491-w\">13. P. Thirawatananond, R. L. McPherson, J. Malhi, S. Nathan, M. J. Lambrecht, M. Brichacek, P. J. Hergenrother, A. K. L. Leung, S. B. Gabelli \u201cStructural analyses of NudT16-ADP-ribose complexes direct rational design of mutants with improved processing of poly(ADP-ribosyl)ated proteins.\u201d <em>Sci. Rep.<\/em> <strong>2019<\/strong>, <em>9<\/em>, 5940.<\/a><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"size-medium wp-image-267 aligncenter\" src=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/PDB-of-Nudt16-with-ADP-Ribose-300x169.jpg\" alt=\"PDB of Nudt16 with ADP Ribose\" width=\"300\" height=\"169\" srcset=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/PDB-of-Nudt16-with-ADP-Ribose-300x169.jpg 300w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/PDB-of-Nudt16-with-ADP-Ribose-1024x576.jpg 1024w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/PDB-of-Nudt16-with-ADP-Ribose-768x432.jpg 768w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/PDB-of-Nudt16-with-ADP-Ribose-105x59.jpg 105w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/PDB-of-Nudt16-with-ADP-Ribose-600x338.jpg 600w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/PDB-of-Nudt16-with-ADP-Ribose-317x178.jpg 317w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/PDB-of-Nudt16-with-ADP-Ribose-423x238.jpg 423w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/PDB-of-Nudt16-with-ADP-Ribose-634x357.jpg 634w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/PDB-of-Nudt16-with-ADP-Ribose-846x476.jpg 846w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/PDB-of-Nudt16-with-ADP-Ribose-951x535.jpg 951w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/PDB-of-Nudt16-with-ADP-Ribose-1268x713.jpg 1268w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/PDB-of-Nudt16-with-ADP-Ribose-320x180.jpg 320w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/PDB-of-Nudt16-with-ADP-Ribose.jpg 1280w\" sizes=\"auto, (max-width: 320px) 85vw, (max-width: 768px) 67vw, (max-width: 1024px) 62vw,300px\" \/><\/p>\n<p><a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja512528p\">12. M. J. Lambrecht*, M. Brichacek*, E. Barkauskaite, A. Ariza, I. Ahel, P. J. Hergenrother \u201cSynthesis of Dimeric ADP-Ribose and its Structure with Human Poly(ADP-Ribose) Glycohydrolase\u201d <em>J. Am. Chem. Soc.<\/em> <strong>2015<\/strong>, <em>137<\/em>, 3558. *Equal Contribution<\/a><\/p>\n<p><a href=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-12-J-Am-Chem-Soc-2015.gif\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-132\" src=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-12-J-Am-Chem-Soc-2015.gif\" alt=\"Pub 12 J Am Chem Soc 2015\" width=\"400\" height=\"238\" \/><\/a><\/p>\n<p><a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/047084289X.rt254.pub2\/abstract\">11. N. A. McGrath, M. Brichacek \u201cTrifluoroperacetic Acid\u201d Encyclopedia of Reagents for Organic Synthesis 2012, John Wiley &amp; Sons Ltd.<\/a><\/p>\n<p>&nbsp;<\/p>\n<p><a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201108261\/abstract\">10. F. Li, D. Calabrese, M. Brichacek, I. Lin, J. T. Njardarson \u201cEfficient Synthesis of Thiopyrans Using a Sulfur-Enabled Anionic Cascade\u201d <em>Angew. Chem. Int. Ed.<\/em> <strong>2012<\/strong>,<em> 51<\/em>, 1938-1941.<\/a><\/p>\n<p><a href=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-10-Angew-Chem-Int-Ed-2012.gif\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-131 size-full\" src=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-10-Angew-Chem-Int-Ed-2012.gif\" alt=\"Pub 10 Angew Chem Int Ed 2012\" width=\"400\" height=\"90\" \/><\/a><\/p>\n<p><a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol200263g\">9. M. Brichacek, M. N. Villalobos, A. Plichta, J. T. Njardarson \u201cStereospecific Ring Expansion of Chiral Vinyl Aziridines\u201d<em> Org. Lett.<\/em> <strong>2011<\/strong>, <em>13<\/em>, 1110-1113.<\/a><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-130\" src=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-9-Org-Lett-2011-300x58.gif\" alt=\"Pub 9 Org Lett 2011\" width=\"400\" height=\"78\" srcset=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-9-Org-Lett-2011-300x58.gif 300w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-9-Org-Lett-2011-105x20.gif 105w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-9-Org-Lett-2011-317x61.gif 317w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-9-Org-Lett-2011-423x82.gif 423w\" sizes=\"auto, (max-width: 320px) 85vw, (max-width: 768px) 67vw, (max-width: 1024px) 62vw,400px\" \/><\/p>\n<p><a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2010\/cc\/c0cc01419b\/unauth#!divAbstract\">8. N. A. McGrath, J. R. Binner, G. Markopoulos, M. Brichacek, J. T. Njardarson \u201cAn Efficient Oxidative Dearomatization-Radical Cyclization Approach to Symmetrically Substituted Bicyclic Guttiferone Natural Products\u201d <em>Chem. Commun<\/em>. <strong>2010<\/strong>, <em>47<\/em>, 209-211.<\/a><\/p>\n<p><a href=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-8-Chem-Commun-2010.gif\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-129\" src=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-8-Chem-Commun-2010-300x50.gif\" alt=\"Pub 8 Chem Commun 2010\" width=\"400\" height=\"67\" srcset=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-8-Chem-Commun-2010-300x50.gif 300w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-8-Chem-Commun-2010-105x18.gif 105w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-8-Chem-Commun-2010-317x53.gif 317w\" sizes=\"auto, (max-width: 320px) 85vw, (max-width: 768px) 67vw, (max-width: 1024px) 62vw,400px\" \/><\/a><\/p>\n<p><a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ed1003806\">7. N. A. McGrath, M. Brichacek, J. T. Njardarson \u201cA Graphical Journey of Innovative Organic Architectures That Have Improved Our Lives\u201d <em>J. Chem. Ed.<\/em> <strong>2010<\/strong>, <em>87<\/em>, 1348-1349.<\/a><\/p>\n<p>&nbsp;<\/p>\n<p><a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ed1003806\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-63 \" src=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Top200BrandNameDrugsbyRetailDollarsin2008v72.jpg\" alt=\"Top 200 rand Name Drugs by Retail Dollars in 2008\" width=\"1165\" height=\"906\" srcset=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Top200BrandNameDrugsbyRetailDollarsin2008v72.jpg 1620w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Top200BrandNameDrugsbyRetailDollarsin2008v72-300x233.jpg 300w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Top200BrandNameDrugsbyRetailDollarsin2008v72-768x597.jpg 768w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Top200BrandNameDrugsbyRetailDollarsin2008v72-1024x796.jpg 1024w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Top200BrandNameDrugsbyRetailDollarsin2008v72-105x82.jpg 105w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Top200BrandNameDrugsbyRetailDollarsin2008v72-317x247.jpg 317w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Top200BrandNameDrugsbyRetailDollarsin2008v72-423x329.jpg 423w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Top200BrandNameDrugsbyRetailDollarsin2008v72-634x493.jpg 634w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Top200BrandNameDrugsbyRetailDollarsin2008v72-846x658.jpg 846w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Top200BrandNameDrugsbyRetailDollarsin2008v72-951x740.jpg 951w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Top200BrandNameDrugsbyRetailDollarsin2008v72-1268x986.jpg 1268w\" sizes=\"auto, (max-width: 320px) 85vw, (max-width: 768px) 67vw, (max-width: 1024px) 62vw,1165px\" \/><\/a><\/p>\n<p><a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040402010004059\">6. M. Brichacek, L. A. Batory, N. A. McGrath, J. T. Njardarson \u201cThe Strategic Marriage of Method and Motif. Total Synthesis of Varitriol\u201d <em>Tetrahedron<\/em> <strong>2010<\/strong>, <em>66<\/em>, 4832-4840.<\/a><\/p>\n<p><a href=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-6-Tetrahedron-2010.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-128\" src=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-6-Tetrahedron-2010-300x105.jpg\" alt=\"Pub 6 Tetrahedron 2010\" width=\"400\" height=\"140\" srcset=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-6-Tetrahedron-2010-300x105.jpg 300w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-6-Tetrahedron-2010-105x37.jpg 105w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-6-Tetrahedron-2010-317x111.jpg 317w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-6-Tetrahedron-2010.jpg 373w\" sizes=\"auto, (max-width: 320px) 85vw, (max-width: 768px) 67vw, (max-width: 1024px) 62vw,400px\" \/><\/a><\/p>\n<p><a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.200906830\/abstract\">5. M. Brichacek, L. A. Batory, J. T. Njardarson \u201cStereoselective Ring Expansion of Vinyl Oxiranes. Mechanistic Insights and Natural Product Total Synthesis\u201d <em>Angew. Chem. Int. Ed.<\/em> <strong>2010<\/strong>, <em>49<\/em>, 1648-1651.<\/a><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-127\" src=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-5-Angew-Chem-Int-Ed-2010.gif\" alt=\"Pub 5 Angew Chem Int Ed 2010\" width=\"300\" height=\"140\" \/><\/p>\n<p><a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2009\/ob\/b900236g#!divAbstract\">4. M. Brichacek, J. T. Njardarson \u201cCreative approaches towards the synthesis of 2,5-dihydro- furans, thiophenes, and pyrroles. One method does not fit all!\u201d <em>Org. Biomol. Chem<\/em>. <strong>2009<\/strong>, <em>7<\/em>, 1761-1770.<\/a><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-126\" src=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-4-Org-Biomol-Chem-2009-300x124.gif\" alt=\"Pub 4 Org Biomol Chem 2009\" width=\"400\" height=\"165\" srcset=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-4-Org-Biomol-Chem-2009-300x124.gif 300w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-4-Org-Biomol-Chem-2009-105x43.gif 105w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-4-Org-Biomol-Chem-2009-317x131.gif 317w\" sizes=\"auto, (max-width: 320px) 85vw, (max-width: 768px) 67vw, (max-width: 1024px) 62vw,400px\" \/><\/p>\n<p><a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.200804237\/abstract\">3. N. A. McGrath, C. A. Lee, H. Araki, M. Brichacek, J. T. Njardarson \u201cAn Efficient Substrate-Controlled Approach Towards Hypoestoxide, a Member of a Family of Diterpenoid Natural Products with an Inside-Out [9.3.1] Bicyclic Core.\u201d<em> Angew. Chem, Int. Ed.<\/em> <strong>2008<\/strong>, <em>47<\/em>, 9450-9453.<\/a><\/p>\n<p><a href=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-3-Angew-Chem-Int-ed-2008.gif\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-125\" src=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-3-Angew-Chem-Int-ed-2008-300x71.gif\" alt=\"Pub 3 Angew Chem Int ed 2008\" width=\"400\" height=\"95\" srcset=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-3-Angew-Chem-Int-ed-2008-300x71.gif 300w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-3-Angew-Chem-Int-ed-2008-105x25.gif 105w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-3-Angew-Chem-Int-ed-2008-317x75.gif 317w\" sizes=\"auto, (max-width: 320px) 85vw, (max-width: 768px) 67vw, (max-width: 1024px) 62vw,400px\" \/><\/a><\/p>\n<p><a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol802123e\">2. M. Brichacek, D. Lee, J. T. Njardarson \u201cLewis Acid Catalyzed [1,3]-Sigmatropic Rearrangement of Vinyl Aziridines\u201d <em>Org. Lett.<\/em> <strong>2008<\/strong>, <em>10<\/em>, 5023-5026.<\/a><\/p>\n<p><a href=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-2-Org-Lett-2008.gif\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-124\" src=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-2-Org-Lett-2008-300x113.gif\" alt=\"Pub 2 Org Lett 2008\" width=\"400\" height=\"150\" srcset=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-2-Org-Lett-2008-300x113.gif 300w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-2-Org-Lett-2008-105x39.gif 105w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-2-Org-Lett-2008-317x119.gif 317w, https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2015\/05\/Pub-2-Org-Lett-2008-423x159.gif 423w\" sizes=\"auto, (max-width: 320px) 85vw, (max-width: 768px) 67vw, (max-width: 1024px) 62vw,400px\" \/><\/a><\/p>\n<p><a href=\"http:\/\/www.tandfonline.com\/doi\/abs\/10.1080\/00397910701557358\">1. M. P. Brichacek, R. M. Carlson \u201cDihydropyran as a Template for Lactone Synthesis\u201d <em>Synthetic Commun.<\/em> <strong>2007<\/strong>,<em> 37<\/em>, 3541-3549.<\/a><\/p>\n<hr \/>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Publications: 17. T. Cheewawisuttichai, M. Brichacek \u201cDevelopment of a multifunctional neoglycoside auxiliary for applications in glycomics research\u201d Org. Biomol. Chem. 2021, 19, 6613-6617. 16. \u00a0A. Numan, M. Brichacek \u201cAsymmetric Synthesis of Stereogenic Phosphorus P(V) Centers Using Chiral Nucleophilic Catalysis\u201d Molecules 2021, 26 (12), 3661. 15. T. Cheewawisuttichai, R. D. Hurst,\u00a0 M. Brichacek \u201cTransformation of aldehydes [&hellip;]<\/p>\n","protected":false},"author":1034,"featured_media":0,"parent":0,"menu_order":4,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_kad_blocks_custom_css":"","_kad_blocks_head_custom_js":"","_kad_blocks_body_custom_js":"","_kad_blocks_footer_custom_js":"","_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"class_list":["post-11","page","type-page","status-publish","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.2 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Publications - Brichacek Lab - University of Maine<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/umaine.edu\/brichlab\/research\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Publications - Brichacek Lab - University of Maine\" \/>\n<meta property=\"og:description\" content=\"Publications: 17. T. Cheewawisuttichai, M. Brichacek \u201cDevelopment of a multifunctional neoglycoside auxiliary for applications in glycomics research\u201d Org. Biomol. Chem. 2021, 19, 6613-6617. 16. \u00a0A. Numan, M. Brichacek \u201cAsymmetric Synthesis of Stereogenic Phosphorus P(V) Centers Using Chiral Nucleophilic Catalysis\u201d Molecules 2021, 26 (12), 3661. 15. T. Cheewawisuttichai, R. D. Hurst,\u00a0 M. Brichacek \u201cTransformation of aldehydes [&hellip;]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/umaine.edu\/brichlab\/research\/\" \/>\n<meta property=\"og:site_name\" content=\"Brichacek Lab\" \/>\n<meta property=\"article:modified_time\" content=\"2021-09-17T01:10:35+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/Tetrazine-neoglycoside-glycan-auxiliary.gif\" \/>\n\t<meta property=\"og:image:width\" content=\"378\" \/>\n\t<meta property=\"og:image:height\" content=\"124\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/gif\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"2 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/umaine.edu\/brichlab\/research\/\",\"url\":\"https:\/\/umaine.edu\/brichlab\/research\/\",\"name\":\"Publications - Brichacek Lab - University of Maine\",\"isPartOf\":{\"@id\":\"https:\/\/umaine.edu\/brichlab\/#website\"},\"primaryImageOfPage\":{\"@id\":\"https:\/\/umaine.edu\/brichlab\/research\/#primaryimage\"},\"image\":{\"@id\":\"https:\/\/umaine.edu\/brichlab\/research\/#primaryimage\"},\"thumbnailUrl\":\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/Tetrazine-neoglycoside-glycan-auxiliary.gif\",\"datePublished\":\"2015-05-07T12:56:42+00:00\",\"dateModified\":\"2021-09-17T01:10:35+00:00\",\"breadcrumb\":{\"@id\":\"https:\/\/umaine.edu\/brichlab\/research\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/umaine.edu\/brichlab\/research\/\"]}]},{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\/\/umaine.edu\/brichlab\/research\/#primaryimage\",\"url\":\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/Tetrazine-neoglycoside-glycan-auxiliary.gif\",\"contentUrl\":\"https:\/\/umaine.edu\/brichlab\/wp-content\/uploads\/sites\/391\/2021\/09\/Tetrazine-neoglycoside-glycan-auxiliary.gif\",\"width\":378,\"height\":124,\"caption\":\"Tetrazine neoglycoside glycan auxiliary\"},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/umaine.edu\/brichlab\/research\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\/\/umaine.edu\/brichlab\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Publications\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/umaine.edu\/brichlab\/#website\",\"url\":\"https:\/\/umaine.edu\/brichlab\/\",\"name\":\"Brichacek Lab\",\"description\":\"University of Maine\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/umaine.edu\/brichlab\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Publications - Brichacek Lab - University of Maine","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/umaine.edu\/brichlab\/research\/","og_locale":"en_US","og_type":"article","og_title":"Publications - Brichacek Lab - University of Maine","og_description":"Publications: 17. 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