Total No. of Publications:
- Self-Assembly of a β-Peptide Foldamer: The Role of the Surfactant in Three-Dimensional Shape Selection J. Gong, T. Eom, W. Lee, A. Roy, S. Kwon, H. Kim and H. –S. Lee, ChemPlusChem, 2019, 84, 481
- Conformationally rigid aromatic amino acids as building blocks for abiotic foldamers. V. V. E. Ramesh, A. Roy, K. N. Vijayadas, A. M. Kendhale, P. Prabhakaran, R. G. Gonnade, V. G. Puranik and G. J. Sanjayan, Org. Biomol. Chem., 2011, 9, 367. (Front Cover page)
- Diversifying the structural architecture of synthetic oligomers: the hetero foldamer approach. A. Roy, P. Prabhakaran, P. K. Baruah and G. J. Sanjayan, Chem. Commun., 2011, 47, 11593. (Front Cover page)
- Sugar–amino acid cyclic conjugates as novel conformationally constrained hydroxy- ethylamine transition-state isosteres. A. Roy and G. J. Sanjayan, Tetrahedron Lett. 2012, 53, 3361.
- Probing the folding induction ability of orthanilic acid in peptides: Some observations. A. Roy, A. S. Kotmale, R. L. Gawade, V. G. Puranik, P. R. Rajamohanan and G. J. Sanjayan, RSC adv., 2014, 4, 13018
- Nucleophilic ring opening of benzoxazinones by DBU: some observations. S. B. Baravkar, A. Roy, R. L. Gawade, V. G. Puranik and G. J. Sanjayan, Synthetic Commun., 2014, 44, 2955.
- Heterogenous foldamers from aliphatic-aromatic amino acid building blocks: current trends and future prospects. R. V. Nair, K. N. Vijayadas, A. Roy and G. J. Sanjayan , Eur. J. Org. Chem., 2014, 7763