References
- W. Tjarks et al., J. Med. Chem. 35, 16228 (1992).
- Y. Yamamoto, Pure Appl. Chem. 63 (3), 423 (1991). doi:10.1351/pac199163030423
- F. Alam et al., J. Med. Chem. 32 (10), 2326 (1989). doi:10.1021/jm00130a017
- M. K. Cyrański et al., Phys. J. Phys. Org. Chem. 21 (6), 472 (2008). doi:10.1002/poc.1389
- A. Vega, M. Zorate, H and Tlahuext, H., Hofl Acta Cryst. 66, 01260 (2010).
- P. J. Stephens et al., J. Phys. Chem. 98 (45), 11623 (1994). doi:10.1021/j100096a001
- F. J. Devlin et al., J. Phys. Chem. 99 (46), 16883 (1995). doi:10.1021/j100046a014
- S. Y. Lee, and B. H. Boo, Bull. Korean Chem. Soc. 17, 754 (1996).
- N. C. Handy, C. W. Murray, and R. D. Amos, J. Phys. Chem. 97 (17), 4392 (1993). doi:10.1021/j100119a023
- D. G. Hall, Structure, properties, and preparation of boronic acid derivatives. Overview of their reactions and applications. In Boronic Acids, First Edn, Wiley-VCH, Weinheim (2005).
- E. Cuthbertson, Boronic Acids: Properties and Applications, Alfa Aesar, Heysham (2006).
- E. Frisch et al., Gauss View 05, Gaussian Inc., Walling Ford, CT USA (2009).
- M. J. Frisch et.al., Gaussian 09W, Revision A.02, Gaussian Inc, Walling Ford, CT (2009).
- J. Choo et al., J. Mol. Struct. (Theochem) 587 (1-3), 1 (2002). doi:10.1016/S0166-1280(02)00107-0
- P. Govindasamy, S. Gunasekaran, and G. R. Ramkumaar, Spectrochim. Acta A Mol. Biomol. Spectrosc. 130, 621 (2014)., doi:10.1016/j.saa.2014.03.065
- M. Karabacak et al., Spectrochim. Acta A Mol. Biomol. Spectrosc. 85 (1), 179 (2012). doi:10.1016/j.saa.2011.09.058
- R. Milton Silverstein et al., Spectrometric Identification of Organic Compounds (John Wiley & Sons, New York, 1981).
- S. Aayisha et al., J. Mol. Struct. 1186, 468 (2019). doi:10.1016/j.molstruc.2019.03.056
- J. A. Faniran, and H. F. Shurvell, Can. J. Chem. 46 (12), 2089 (1968). doi:10.1139/v68-341
- S. Muthu et al., J. Mol. Struct. 1081, 400 (2014). doi:10.1016/j.molstruc.2014.10.024
- M. Szafran, A. Komasa, and E. B. Adamska, J. Mol. Struct. (Theochem.) 827 (1-3), 101 (2007). doi:10.1016/j.molstruc.2006.05.012
- C. James et al., J. Raman Spectrosc. 37 (12), 1381 (2006). doi:10.1002/jrs.1554
- S. Ayyappan et al., J. Raman Spectrosc. 41 (10), 1379 (2010). doi:10.1002/jrs.2576
- O. Alver, and C. Parlak, Vib. Spectrosc. 54 (1), 1 (2010). doi:10.1016/j.vibspec.2010.05.001
- U. Rani et al., Spectrochim. Acta A Mol. Biomol. Spectrosc. 92, 67 (2012). doi:10.1016/j.saa.2012.02.036
- D. Debnath et al., Spectrochim. Acta A Mol. Biomol. Spectrosc. 140, 185 (2015). doi:10.1016/j.saa.2014.12.027
- C. Kemnitz Chemoffice Ultra, Trial Version. Perkin Elmer informatics. Cambridge (MA). Cambridge soft; 2002.
- M. Prabhaharan et al., Mol. Biomol. Spectrosc. 136, 494 (2015). doi:10.1016/j.saa.2014.09.062
- S. Seshadri et al., J. Raman Spectrosc. 38 (11), 1523 (2007). doi:10.1002/jrs.1808
- D. Shoba et al., Spectrochim. Acta A Mol. Biomol. Spectrosc. 118, 438 (2014). doi:10.1016/j.saa.2013.09.023
- E. Y. Chien et al., Science 330 (6007), 1091 (2010). doi:10.1126/science.1197410
- T. K. Kuruvilla et al., J. Mol. Struct. 1175, 163 (2019). doi:10.1016/j.molstruc.2018.07.097
- M. Govindarajan et al., Spectrochim. Acta A Mol. Biomol. Spectrosc. 97, 231 (2012). doi:10.1016/j.saa.2012.06.014
- S. Ramalingam et al., Spectrochim. Acta A Mol. Biomol. Spectrosc. 76 (1), 84 (2010). doi:10.1016/j.saa.2010.02.050
- S. Sahaya Sathish, and N. Janakiraman, Int. J. Pharmaceut. Sci. Drug Res. 4 (1), 56 (2012).