Abstract
Depending on the substituent on the phosphorus(III) atom, reactions of tris(dialkylamino)phosphines, 2-diethylamino-1,3,2-benzodioxaphosphole, and benzene-1,4-diylbis(N,N,N′,N′-tetraethylphosphonous diamide) with 1-alkylisatins lead to the formation of isoindigo derivatives, spirophosphoranes, or spirooxiranes whose structure was determined by NMR spectroscopy and X-ray analysis.
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Dedicated to Full Member of the Russian Academy of Sciences O.N. Chupakhin on his 80th anniversary
Original Russian Text © L.I. Musin, A.V. Bogdanov, D.B. Krivolapov, A.B. Dobrynin, I.A. Litvinov, V.F. Mironov, 2014, published in Zhurnal Organicheskoi Khimii, 2014, Vol. 50, No. 6, pp. 839–845.
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Musin, L.I., Bogdanov, A.V., Krivolapov, D.B. et al. Effect of the substituent on the phosphorus atom on the reaction of aminophosphines with 1-alkylisatins. Russ J Org Chem 50, 822–828 (2014). https://doi.org/10.1134/S1070428014060116
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DOI: https://doi.org/10.1134/S1070428014060116