5^th Global Chemistry Congress

Some environment friendly greener methodologies have been described for the synthesis of new isoxazolidine and isoxazoline derivatives using new nitrones via 1,3-dipolar cycloaddition reactions. These also include synthesis of bisisoxazolidine and bisisoxazoline derivatives synthesized from glyoxal and terepthalaldehyde respectively. Few new spiro isoxazolidine derivatives have been also reported using new dipolarophiles. Furthermore, these new isoxazolidine and isoxazoline derivatives are found to have vast synthetic potential as they could be used as precursors for the synthesis of a variety of new organic molecules including peptides, 1,3-amino alcohols with potential biological activities. For the synthesis of peptides, it has been observed that CDMT (chloro dimethyl triazine) has found to be better coupling reagent than conventional DCC (dicyclohexyl carbodiamide)due to the formation of insoluble by-product (N,N-dicyclohexylurea)and purification becomes tedious.The new nitrones reported are synthesized from dihydropyran, chlorohydrin and formamide respectively. Significant increase in the reaction rates, excellent yields, and high selectivity (diastereo and regioselectivity) are the important features observed in these cycloaddition reactions following greener methodologies. It has been observed that high diastereoselectivity in these cycloaddition reactions have been observed when the reactions are performed in water. Synthesis of aldehydes and ketones with new nitrones in atom efficient reactions are the most attractive features as they have future scopes in these reactions. The side products (enamines) obtained during the synthesis of aldehydes and ketones has been successfully utilized as new dipolarophiles in these cycloaddition reactions for the synthesis of spiro

cycloadducts.

 

Recent Publications:

1. Yao, T.; Liu, D.; Zhang, C. “Palladium-catalyzed domino Heck/intermol ecular cross-coupling: efficient synthesis of 4-alkylated isoquinoline derivatives” Chem. Commun. 2017, 53, 2386.
2. Yao, T.; Dan, H. “Palladium-Catalyzed Domino Heck/Aryne Carbopalladation/C-H Functionalization:Synthesis of Heterocycle-Fused 9,10-Dihydrophenanthrenes”, Org. Lett. 2017, 19, 842
3. Yao, T.; Zhang, H.; Zhao, Y. “Synthesis of 9,10-Phenanthrenes via Palladium-Catalyzed Aryne Annulation by o-Halostyrenes and Formal Synthesis of (±)-Tylophorine”, Org. Lett. 2016, 18, 2532.
4. Yao, T. “Facile N-arylation of amidines and N,N-disubstituted amidines”, Tetrahedron Lett. 2015, 56, 4623.
5. Schroeder, C. E.; Yao, T.; Sotsky, J. B.; Smith, R. A.; Roy, S.; Chu, Y. K.; Guo, H.; Tower, N. A.; Noah, J. W.; McKellip, S.; Sosa, M.; Rasmussen, L.; Smith, L. H.; White, E. L.; Aubé, J.; Jonsson, C. B.; Chung, D.-H.; Golden, J. E. “Development of (E)-2-((1,4-dimethylpi-perazin-2-ylidene)amino)-5-nitro-N-phenylbenzamide, ML336: novel2-amidinophenylbenzamides as potent inhibitors of Venezuelan equine encephalitis virus”. J. Med. Chem. 2014, 57, 8608..