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Regioselective Three Component Domino Synthesis of Polyhydrospiro[indoline-3,3'-pyrrolizine]-2-one via [3+2] Cycloaddition Reaction
Corresponding Author(s) : Vishwa Deepak Tripathi
Asian Journal of Chemistry,
Vol. 31 No. 3 (2019): Vol 31 Issue 3
Abstract
In present work, we have reported the synthesis and characterisation of novel hexahydrospiro[indoline-3,3′-pyrrolizine]-2-one derivatives in good to excellent yields via [3+2] cycloaddtion reaction in regioselective manner. These compounds were synthesized via multicomponent reaction of substituted 3-cinnamoyl-4-hydroxy-6-methyl-2H-pyran-2-one, isatin, L-proline at room temperature. All the synthesized hexahydrospiro molecules were characterized by 1H and 13C NMR, IR spectra, mass spectra and elemental analysis. Regioselectivity in synthesized molecules were also explained on the basis of secondary orbital interactions. A simple and facile methodology is developed which has great importance in synthetic chemistry.
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References
C. Marti and E.M. Carreira, Eur. J. Org. Chem., 2209 (2003); https://doi.org/10.1002/ejoc.200300050.
C.J. Douglas and L.E. Overman, Proc. Natl. Acad. Sci. USA, 101, 5363 (2004); https://doi.org/10.1073/pnas.0307113101.
B.M. Trost and C. Jiang, Synthesis, 369 (2006); https://doi.org/10.1055/s-2006-926302.
Q. Wei and L.Z. Gong, Lett., 12, 1008 (2010); https://doi.org/10.1021/ol100020v.
G. Pandey, P. Banerjee and S.R. Gadre, Chem. Rev., 106, 4484 (2006); https://doi.org/10.1021/cr050011g.
Z.P. Wang, S. Xiang, P.L. Shao and Y. He, J. Org. Chem., 83, 10995 (2018); https://doi.org/10.1021/acs.joc.8b01622.
J. Jayashankaran, R. Manian, R. Venkatesan and R. Raghunathan, Tetrahedron, 61, 5595 (2005); https://doi.org/10.1016/j.tet.2005.03.088.
P. Shanmugam, B. Viswambharan, K. Selvakumar and S. Madhavan, Tetrahedron Lett., 49, 2611 (2008); https://doi.org/10.1016/j.tetlet.2008.02.104.
T. Yamashita, K. Yasuda, H. Kizu, Y. Kameda, A.A. Watson, R.J. Nash, G.W.J. Fleet and N. Asano, J. Nat. Prod., 65, 1875 (2002); https://doi.org/10.1021/np020296h.
J.W. Daly, T.F. Spande, N. Whittaker, R.J. Highet, D. Feigl, N. Noshimori, T. Tokuyama and C.W. Meyers, J. Nat. Prod., 49, 265 (1986); https://doi.org/10.1021/np50044a012.
C.C. Moldoveanu, P.G. Jones and I.I. Mangalagiu, Tetrahedron Lett., 50, 7205 (2009); https://doi.org/10.1016/j.tetlet.2009.10.044.
J. Kobayashi, M. Tsuda, K. Agemi, H. Shigemori, M. Ishibashi, T. Sasaki and Y. Mikami, Tetrahedron, 47, 6617 (1991); https://doi.org/10.1016/S0040-4020(01)82314-0.
D.M. James, H.B. Kunze and D.J. Faulkner, J. Nat. Prod., 54, 1137 (1991); https://doi.org/10.1021/np50076a040.
G. Periyasami, R. Raghunathan, G. Surendiran and N. Mathivanan, Eur. J. Med. Chem., 44, 959 (2009); https://doi.org/10.1016/j.ejmech.2008.07.009.
H. Miyamoto, Y. Okawa, A. Nakazaki and S. Kobayashi, Angew. Chem. Int. Ed., 45, 2274 (2006); https://doi.org/10.1002/anie.200504247.
A.B. Dounay and L.E. Overman, Chem. Rev., 103, 2945 (2003); https://doi.org/10.1021/cr020039h.
S.T. Hilton, T.C. Ho, G. Pljevalijcic and K. Jones, Org. Lett., 2, 2639 (2000); https://doi.org/10.1021/ol0061642.
S.N. Pandeya, D. Sriram, G. Nath and E. De Clercq, Indian J. Pharm. Sci., 61, 358 (1999).
S.N. Pandeya, D. Sriram, G. Nath and E. De Clercq, Sci. Pharm., 67, 103 (1999).
R. Murugan, S. Anbazhagan and S. Sriman Narayanan, Eur. J. Med. Chem., 44, 3272 (2009); https://doi.org/10.1016/j.ejmech.2009.03.035.
A.D. Borthwick, G. Weingarten, T.M. Haley, M. Tomaszewski, W. Wang, Z. Hu, J. Bedard, H. Jin, L. Yuen and T.S. Mansour, Bioorg. Med. Chem. Lett., 8, 365 (1998); https://doi.org/10.1016/S0960-894X(98)00032-8.