Publication List

Authored research manuscripts and technical reviews

  1. “Photodynamic inactivation of methicillin-resistant Staphylococcus aureus and Escherichia coli: A metalloporphyrin comparison.” Skwor, T.A.; Klemm, S.; Zhang, H.; Schardt, S.; Blaszczyk, S.A.; Bork, M. J. Photochem. Photobiol. B. 2016, 165, 51-57.
  2. “Transition metal mediated carbonylative benzannulations.” Song, W.; Blaszczyk, S.A.; Liu, J.; Wang, S.; Tang, W. Org. Biomol. Chem. 2017, 15, 7490-7504.
  3. “Isoquinoline-1-carboxylate as a traceless leaving group for chelation-assisted glycosylation under mild and neutral reaction conditions.” Wang, H-Y.; Simmons, C.J.; Blaszczyk, S.A.; Balzer, P.G.; Luo, R.; Duan, X.; Tang, W. Angew. Chem. Int. Ed. 2017, 56 (49), 15698-15702.
  4. “Addressing the challenge of carbohydrate site selectivity by synergistic catalysis.” Blaszczyk, S.A.; Tang, W. Chem. 2017, 3, 722-723.
  5. “Chiral reagents in glycosylation and modification of carbohydrates.” Wang, H-Y.; Blaszczyk, S.A; Xiao, G.; Tang, W. Chem. Soc. Rev. 2018, 47, 681-701.
  6. “Recent advances in site-selective functionalization of carbohydrates mediated by organocatalysts.” Blaszczyk, S.A.; Homan, T.; Tang, W. Carb. Res. 2019, 471, 64-77.
  7. “Site- and stereoselective phosphoramidation of carbohydrates using a chiral catalyst and chiral electrophile.” Glazer, D.A.; Schroeder, J.M.; Blaszczyk, S.A.; Tang, W. 2019, 361, 3729 – 3732.
  8. “S-adamantyl directed site-selective acylation and its use in the streamlined synthesis of oligosaccharides.” Blaszczyk, S.A.; Xiao, G.; Wen, P.; Wu, J.; Wang, B.; Carattino, F.; Li, Z.; Liu, P.; Tang, W. Angew. Chem. Int. Ed. 2019, 58, 9542 – 9546.
  9. “A diversification strategy for the synthesis of polycyclic scaffolds with medium-sized rings from complex natural products.” Zhao, C.; Ye, Z.; Ma, Z-x, Blaszczyk, S.A.; Wildman, S.A.; Hu, L.; Tang. W. Nat. Comm. 2019, https://doi.org/10.1038/s41467-019-11976-2 .
  10. “Rhodium-Catalyzed (5 + 2) and (5 + 1) Cycloadditions Using 1,4-Enynes as Five-Carbon Building Blocks.” Blaszczyk, S.A.; Glazier, D. A.; Tang, W. Acc. Chem. Res. 2019, https://doi.org/10.1021/acs.accounts.9b00477.
  11. “Synthesis of glycosyl halides by chelation assisted activation of picolinic esters under mild neutral  conditions.” Wen, P.; Simmons, C.J.; Blaszczyk, S.A.; McCarty, B.; Balzer, P.G.; Tang, W.  Manuscript submitted to Org. Lett.
  12. Blaszczyk, S.A.; Tang, W. Invited account in preparation for SynLett.
  13. Blaszczyk, S.A.; Tang, W. Invited account in preparation for Chem. Rev.

Edited Manuscripts

  1. “Stereoselective Total Synthesis of Hetisine‐type C20‐Diterpenoid Alkaloids: Spirasine IV and XI Stereoselective Total Synthesis of Hetisine-type C20-Diterpenoid Alkaloids: Spirasine IV and XI” Zhang, Q.; Zhongshan, Z.; Huang, Z.; Zhang, C.; Xi, S.; Zhang, M. Angew. Chem. Int. Ed. 2018, 57, 937-94.
  2. “Well-Designed Phosphine–Urea Ligand for Highly Diastereo- and Enantioselective 1,3-Dipolar Cycloaddition of Methacrylonitrile: A Combined Experimental and Theoretical Study” Xiong, Y.; Du, Z.; Chen, H.; Yang, Z.; Tan, Q.; Zhang, C.; Zhu, L.; Lan, Y.; Zhang, M. J. Am. Chem. Soc. 2019, 141 (2), 961-971.
  3. “De novo synthesis of mono- and oligosaccharides via dihydropyran intermediates” Song, W.; Wang, S.; Tang, W. Chem. Asian J. 2017, 12 (10), 1027-1042.
  4. “Iridium-catalyzed highly efficient chemoselective reduction of aldehydes in water using formic acid as the hydrogen source”
    Yang, Z.; Zhu, Z.; Luo, R.; Qiu, X.; Liu, J.-L.; Yang, J.-K.; and Tang W.* Green Chem. 2017, 19, 3296-3301.
  5. “Iridium-Catalyzed Dynamic Kinetic Stereoselective Allylic Etherification of Achmatowicz Rearrangement Products”
    Zhu, Z.; Wang, H.-Y.; Simmons, C. J.; Tseng, P.-S.; Qiu, X.; Zhang, Y.; Duan, X.; Yang, J.-K.; and Tang W.* Adv. Syn. Cat. 2018, 360, 595-599.
  6. “Catalytic Asymmetric Synthesis of All Possible Stereoisomers of 2,3,4,6‐Tetradeoxy‐4‐Aminohexopyranosides” Zhu Z.; Glazier, D. A.; Yang D.; Tang, W.* Adv. Syn. Cat. 2018, 360, 2211-2215.
  7. “Development of the first small molecule histone deacetylase 6 (HDAC6) degraders.” Yang, K.; Song, Y.; Xie, H.; Wu, H.; Wu, Y.-T.; Leisten, E. D.;  Tang W.* Bioorg. Med. Chem. Lett. 2018, 28, 2493-2497.
  8. “Organocatalyst-Mediated Dynamic Kinetic Enantioselective Acylation of 2-Chromanols” Glazier, D. A.; Schroeder, J. M.; Liu, J.; Tang, W.* Adv. Syn. Cat. 2018, 360, 4646-4649.
  9. “Intermolecular Regio- and Stereoselective Hetero-[5+2] Cycloaddition of Oxidopyrylium Ylides and Cyclic Imines” Zhao, C.; Glazier, D. A.; Yang, D.; Yin, D.; Guzei, I. A.; Aristov, M. M.; Liu, P.* and Tang, W.* Angew. Chem. Eng. Ed.  2018, 58, 887-891