Abstract:
2-(2-Oxo-1,2-dihydro-3H-indol-3-ylidene)acetonitriles were subjected to cycloaddition reactions at the double bond affording spiroindole melatonin analogues.
Citation:
N. A. Lozinskaya, M. S. Volkova, M. Yu. Seliverstov, V. V. Temnov, S. E. Sosonyuk, M. V. Proskurnina, N. S. Zefirov, “Syntheses of spiroindole melatonin analogues via 2-(indolin-3-ylidene)acetonitrile cycloadditions”, Mendeleev Commun., 24:5 (2014), 260–261
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https://www.mathnet.ru/eng/mendc2544
https://www.mathnet.ru/eng/mendc/v24/i5/p260
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N.B. Chesnokova, O.V. Beznos, N.A. Lozinskaya, M.S. Volkova, E.V. Zaryanova, N.A. Zefirov, A.V. Grigoryev, “Novel agonists of melatonin receptors as promising hypotensive and neuroprotective agents for therapy of glaucoma”, BIOMED KHIM, 63:1 (2017), 75
N. B. Chesnokova, O. V. Beznos, N. A. Lozinskaya, M. S. Volkova, E. V. Zaryanova, N. S. Zefirov, A. V. Grigoryev, “Novel agonists of melatonin receptors as promising hypotensive and neuroprotective agents for therapy of glaucoma”, Biochem. Moscow Suppl. Ser. B, 11:3 (2017), 272
Yan Lu, Yuhang Zhou, Lili Lin, Haifeng Zheng, Kai Fu, Xiaohua Liu, Xiaoming Feng, “N,N′-Dioxide/nickel(ii)-catalyzed asymmetric Diels–Alder reaction of cyclopentadiene with 2,3-dioxopyrrolidines and 2-alkenoyl pyridines”, Chem. Commun., 52:53 (2016), 8255
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