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S. R.  Shirsath, Shinde, G. H., Shaikh, A. C., and Muthukrishnan, M., ? Accessing alpha-arylated nitriles via BF3 center dot OEt2 catalyzed cyanation of para-quinone methides using tert-butyl isocyanide as a cyanide source?, Journal of Organic Chemistry, vol. 83, no. 19, pp. 12305-12314, 2018.\par \par G. S.  Ghotekar, Shirsath, S. R., Shaikh, A. C., and Muthukrishnan, M., ?1,6-Conjugate addition initiated formal [4+2] annulation of p-quinone methides with sulfonyl allenols: a unique access to spiro[5.5]undeca-1,4-dien-3-one scaffolds?, Chemical Communications, vol. 56, no. 37, pp. 5022-5025, 2020.\par \par S. R.  Shirsath, Ghotekar, G. S., Bahadur, V., Gonnade, R. G., and Muthukrishnan, M., ?Silver-catalyzed cascade cyclization/1,6-conjugate addition of homopropargyl sulfonamides to p-quinone methides: an approach to diverse 3-diarylmethine substituted dihydropyrroles?, Journal of Organic Chemistry, vol. 85, no. 23, pp. 15038-15050, 2020.\par \par S. R.  Shirsath, Chandgude, S. M., and Muthukrishnan, M., ?Iron catalyzed tandem ring opening/1,6-conjugate addition of cyclopropanols with p-quinone methides: new access to gamma,gamma-diaryl ketones?, Chemical Communications, vol. 57, no. 99, pp. 13582-13585, 2021.\par \par S. R.  Shirsath, Sable, S. S., Gaikwad, S. G., and Gogate, P. R., ?Ultrasound assisted curcumin recovery from Curcuma aromatica: understanding the effect of different operating parameters?, Chemical Engineering and Processing-Process Intensification, vol. 169, p. 108604, 2021.\par \par S. R.  Shirsath, More, D. A., and Muthukrishnan, M., ?Metal-free aminocarbonylation of p-quinone methides with isocyanides: synthesis of sterically hindered alpha-arylated acetamides?, Chemistry-an Asian Journal, vol. 17, no. 20, p. e202200642, 2022.\par \par D. A.  More, Shirsath, S. R., and Muthukrishnan, M., ?Metal- and photocatalyst-free, visible-light-initiated C3 a-aminomethylation of quinoxalin-2(1H)-ones via electron donor-acceptor complexes?, Journal of Organic Chemistry, vol. 88, no. 18, pp. 13339-13350, 2023.\par \par }