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Journal Article
A. B. Viveki, Garad, D. N., Gonnade, R. G., and Mhaske, S. B., Para-selective copper-catalyzed C(sp(2))-H amidation/dimerization of anilides via a radical pathway, Chemical Communications, vol. 56, no. 10, pp. 1565-1568, 2020.
J. P. Mahajan, Suryawanshi, Y. R., and Mhaske, S. B., Pd-Catalyzed imine cyclization: synthesis of antimalarial natural products aplidiopsamine A, marinoquinoline A, and their potential hybrid NCLite-M1, Organic Letters, vol. 14, no. 22, pp. 5804-5807, 2012.
D. N. Garad, Viveki, A. B., and Mhaske, S. B., Pd-catalyzed regioselective mono-arylation: quinazolinone as the inherent directing group for C(sp(2))-H activation, Journal of Organic Chemistry, vol. 82, no. 12, pp. 6366-6372, 2017.
D. N. Garad and Mhaske, S. B., Pd(II)-catalyzed intramolecular tandem olefin amidation/C-H activation protocol for the syntheses of the protoberberine class of natural products, Organic Letters, vol. 18, no. 15, pp. 3862-3865, 2016.
V. Yadav, Balaraman, E., and Mhaske, S. B., Phosphine-free manganese(II)-catalyst enables acceptorless dehydrogenative coupling of alcohols with indoles, Advanced Synthesis & Catalysis, vol. 363, no. 18, pp. 4430-4439, 2021.
R. Tiwari, Shinde, P. S., Sreedharan, S., Dey, A. Kumar, Vallis, K. A., Mhaske, S. B., Pramanik, Skumar, and Das, A., Photoactivatable prodrug for simultaneous release of mertansine and CO along with a BODIPY derivative as a luminescent marker in mitochondria: a proof of concept for NIR image-guided cancer therapy, Chemical Science, vol. 12, no. 7, pp. 2667-2673, 2021.
P. Halder and Mhaske, S. B., PIDA-mediated N-N bond formation to access pyrazolidine-3,5-diones: a novel process for uricosuric agents G-25671 and sulfinpyrazone, Chemical Communications, vol. 59, no. 53, pp. 8242-8245, 2023.
P. S. Mahajan, Gonnade, R. G., and Mhaske, S. B., Protecting-group-free diastereoselective total synthesis of (+/-)-6-epi-cleistenolide and chemoenzymatic synthesis of (-)-6-epi-cleistenolide, European Journal of Organic Chemistry, no. 36, pp. 8049-8054, 2014.