Matthew M. Bio, Ph.D. - Publications

Affiliations: 
2001 Columbia University, New York, NY 
Area:
Organic synthesis

30 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
2020 Monfette S, Fang Y, Bio MM, Brown AR, Crouch IT, Desrosiers J, Duan S, Hawkins JM, Hayward CM, Peperni N, Rainville JP. Continuous Process for Preparing the Difluoromethylating Reagent [(DMPU)2Zn(CF2H)2] and Improved Synthesis of the ICHF2 Precursor Organic Process Research & Development. 24: 1077-1083. DOI: 10.1021/Acs.Oprd.0C00089  0.456
2020 Breen CP, Parrish C, Shangguan N, Majumdar S, Murnen H, Jamison TF, Bio MM. A Scalable Membrane Pervaporation Approach for Continuous Flow Olefin Metathesis Organic Process Research & Development. 24: 2298-2303. DOI: 10.1021/Acs.Oprd.0C00061  0.315
2018 Li H, Breen CP, Seo H, Jamison TF, Fang YQ, Bio MM. Ni-Catalyzed Electrochemical Decarboxylative C-C Couplings in Batch and Continuous Flow. Organic Letters. PMID 29431449 DOI: 10.1021/Acs.Orglett.8B00070  0.396
2017 Li H, Sheeran JW, Clausen AM, Fang YQ, Bio MM, Bader S. Flow Asymmetric Propargylation: Development of Continuous Processes for the Preparation of a Chiral β-Amino Alcohol. Angewandte Chemie (International Ed. in English). PMID 28685962 DOI: 10.1002/Anie.201704882  0.349
2017 Fang Y, Li H, Sheeran JW, Clausen AM, Bio MM, Bader S. Flow Asymmetric Propargylation: Development of Continuous Processes for a Chiral beta-Amino Alcohol Angewandte Chemie. DOI: 10.1002/Ange.201704882  0.345
2016 Beaver MG, Langille NF, Cui S, Fang Y, Bio MM, Potter-Racine MS, Tan H, Hansen KB. Crystallization-Induced Dynamic Resolution of a Diarylmethylamine toward the Synthesis of a Potent TRPM8 Inhibitor Organic Process Research & Development. 20: 1341-1346. DOI: 10.1021/Acs.Oprd.6B00162  0.409
2015 Chen Y, Huang J, Hwang TL, Chen MJ, Tedrow JS, Farrell RP, Bio MM, Cui S. Highly Regioselective Halogenation of Pyridine N-Oxide: Practical Access to 2-Halo-Substituted Pyridines. Organic Letters. 17: 2948-51. PMID 26037223 DOI: 10.1021/Acs.Orglett.5B01057  0.322
2015 Mennen SM, Mak-Jurkauskas ML, Bio MM, Hollis LS, Nadeau KA, Clausen AM, Hansen KB. Synthesis of 4-Substituted Phthalazin-1(2H)-ones from 2-Acylbenzoic Acids: Controlling Hydrazine in a Pharmaceutical Intermediate through PAT-Guided Process Development Organic Process Research and Development. 19: 884-891. DOI: 10.1021/Acs.Oprd.5B00135  0.359
2013 Huckins JR, Bercot EA, Thiel OR, Hwang TL, Bio MM. Rh(III)-catalyzed C-H activation and double directing group strategy for the regioselective synthesis of naphthyridinones. Journal of the American Chemical Society. 135: 14492-5. PMID 24020333 DOI: 10.1021/Ja405140F  0.44
2013 Cleator E, Scott JP, Avalle P, Bio MM, Brewer SE, Davies AJ, Gibb AD, Sheen FJ, Stewart GW, Wallace DJ, Wilson. RD. Process Development and Multikilogram-Scale Synthesis of a TRPV1 Antagonist Organic Process Research and Development. 17: 1561-1567. DOI: 10.1021/Op400304H  0.51
2012 Nkepang G, Pogula PK, Bio M, You Y. Synthesis and singlet oxygen reactivity of 1,2-diaryloxyethenes and selected sulfur and nitrogen analogs Photochemistry and Photobiology. 88: 753-759. PMID 22268454 DOI: 10.1111/J.1751-1097.2012.01095.X  0.308
2012 Chen Y, Huang J, Hwang TL, Li TJ, Cui S, Chan J, Bio M. A highly regioselective Friedländer reaction mediated by lanthanum chloride Tetrahedron Letters. 53: 3237-3241. DOI: 10.1016/J.Tetlet.2012.04.038  0.457
2011 Chan J, Burke BJ, Baucom K, Hansen K, Bio MM, DiVirgilio E, Faul M, Murry J. Practical syntheses of a CXCR3 antagonist. The Journal of Organic Chemistry. 76: 1767-74. PMID 21299207 DOI: 10.1021/Jo102399A  0.454
2010 Fang YQ, Bio MM, Hansen KB, Potter MS, Clausen A. Magnesium coordination-directed n-selective stereospecific alkylation of 2-pyridones, carbamates, and amides using α-halocarboxylic acids. Journal of the American Chemical Society. 132: 15525-7. PMID 20958067 DOI: 10.1021/Ja107709W  0.408
2010 Asselin SM, Bio MM, Langille NF, Ngai KY. Practical access to metallo thiophenes: Regioselective synthesis of 2,4-disubstituted thiophenes Organic Process Research and Development. 14: 1427-1431. DOI: 10.1021/Op100226K  0.466
2009 Wilson RD, Cleator E, Ashwood MS, Bio MM, Brands KMJ, Davies AJ, Dolling UH, Emerson KM, Gibb AD, Hands D, McKeown AE, Oliver SF, Reamer RA, Sheen FJ, Stewart GW, et al. Development of a scaleable synthesis of a partial nicotinic acid receptor agonist Organic Process Research and Development. 13: 543-547. DOI: 10.1021/Op800290T  0.447
2009 Bio MM, Cleator E, Davies AJ, Hamilton SE, Lawrence A, Sheen FJ, Stewart GW, Wilson RD. Regioselective coupling reactions of 2,4-diaminopyridine derivatives with aryl halides: the synthesis of elaborated pyridines Tetrahedron. 65: 8950-8955. DOI: 10.1016/J.Tet.2009.08.056  0.437
2008 Bio MM, Waters M, Javadi G, Song ZJ, Zhang F, Thomas D. An efficient synthesis of an NMDA receptor antagonist via stereoselective fluorination Synthesis. 891-896. DOI: 10.1055/S-2008-1032181  0.439
2008 Bio MM, Hansen KB, Gipson J. A practical, efficient synthesis of 1,1-dioxo-hexahydro-1#-thiopyran-4- carbaldehyde Organic Process Research and Development. 12: 892-895. DOI: 10.1021/Op800108S  0.45
2007 Alorati AD, Bio MM, Brands KMJ, Cleator E, Davies AJ, Wilson RD, Wise CS. A practical and scaleable synthesis of 1r,5s-bicyclo[3.1.0]hexan-2-one: The development of a catalytic lithium 2,2,6,6-tetramethylpiperidide (LTMP) mediated intramolecular cyclopropanation of (R)-1,2-epoxyhex-5-ene Organic Process Research and Development. 11: 637-641. DOI: 10.1021/Op700042W  0.345
2007 Klingensmith LM, Bio MM, Moniz GA. Selective protodeboronation: synthesis of 4-methyl-2-thiopheneboronic anhydride and demonstration of its utility in Suzuki-Miyaura reactions Tetrahedron Letters. 48: 8242-8245. DOI: 10.1016/j.tetlet.2007.09.060  0.359
2006 Cleator E, Sheen FJ, Bio MM, Jos Brands KM, Davies AJ, Dolling UH. Regioselective synthesis of N-substituted-4-substituted isothiazolidine-1,1-dioxides Tetrahedron Letters. 47: 4245-4248. DOI: 10.1016/J.Tetlet.2006.04.038  0.467
2006 Tellers DM, Bio M, Song ZJ, McWilliams JC, Sun Y. Enantioselective hydrogenation of an α-alkoxy substituted ketone with chiral ruthenium (phosphinoferrocenyl)oxazoline complexes Tetrahedron Asymmetry. 17: 550-553. DOI: 10.1016/J.Tetasy.2005.12.028  0.375
2005 Bio MM, Javadi G, Song ZJ. An improved synthesis of N-isocyanoiminotriphenylphosphorane and its use in the preparation of diazoketones Synthesis. 19-21. DOI: 10.1055/S-2004-834928  0.426
2004 Bio MM, Xu F, Waters M, Williams JM, Savary KA, Cowden CJ, Yang C, Buck E, Song ZJ, Tschaen DM, Volante RP, Reamer RA, Grabowski EJ. Practical synthesis of a potent hepatitis C virus RNA replication inhibitor. The Journal of Organic Chemistry. 69: 6257-66. PMID 15357584 DOI: 10.1021/Jo0491096  0.376
2004 Song ZJ, King AO, Waters MS, Lang F, Zewge D, Bio M, Leazer JL, Javadi G, Kassim A, Tschaen DM, Reamer RA, Rosner T, Chilenski JR, Mathre DJ, Volante RP, et al. An efficient asymmetric synthesis of an estrogen receptor modulator by sulfoxide-directed borane reduction Proceedings of the National Academy of Sciences of the United States of America. 101: 5776-5781. PMID 15079059 DOI: 10.1073/Pnas.0307415101  0.421
2003 Bio MM, Leighton JL. An approach to the synthesis of the phomoidrides Journal of Organic Chemistry. 68: 1693-1700. PMID 12608780 DOI: 10.1021/Jo026478Y  0.607
2000 Bio MM, Leighton JL. Stereoconvergent palladium-catalyzed carbonylation of both E and Z isomers of a 2-trifloxy-1,3-butadiene. Organic Letters. 2: 2905-7. PMID 10964395 DOI: 10.1021/Ol0063609  0.601
2000 Bio MM, Leighton JL. Stereoconvergent palladium-catalyzed carbonylation of both E and Z isomers of a 2-trifloxy-1,3-butadiene Organic Letters. 2: 2905-2907.  0.541
1999 Bio MM, Leighton JL. An approach to the synthesis of CP-263,114: A remarkably facile silyloxy-Cope rearrangement [18] Journal of the American Chemical Society. 121: 890-891. DOI: 10.1021/Ja983609X  0.583
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