DOI QR코드

DOI QR Code

A Practical and Stereoselective Synthesis of Cinnamyl Alcohols Bearing α-Cyano or α-Ester Functional Group from Baylis-Hillman Adducts

  • Lee, Ka-Young (Department of Chemistry and Institute of Basic Science, Chonnam National University) ;
  • GowriSankar, Saravanan (Department of Chemistry and Institute of Basic Science, Chonnam National University) ;
  • Kim, Jae-Nyoung (Department of Chemistry and Institute of Basic Science, Chonnam National University)
  • Published : 2004.03.20

Abstract

Keywords

References

  1. Basavaiah, D.; Padmaja, K.; Satyanarayana, T. Synthesis 2000,1662 and further references cited therein.
  2. Basavaiah, D.; Rao,A. J.; Satyanarayana, T. Chem. Rev. 2003, 103, 811. https://doi.org/10.1021/cr010043d
  3. Basavaiah, D.; Kumaragurubaran, N.; Padmaja, K. Synlett 1999,1630.
  4. Kim, H. S.; Kim, T. Y.; Lee, K. Y.; Chung, Y. M.; Lee, H. J.; Kim,J. N. Tetrahedron Lett. 2000, 41, 2613. https://doi.org/10.1016/S0040-4039(00)00229-X
  5. Shanmugam, P.; Singh, P. R. Synlett 2001, 1314.
  6. Shanmugam,P.; Rajasingh, P. Chem. Lett. 2002, 1212.
  7. Mason, P. H.; Emslie, N. D. Tetrahedron 1994, 50, 12001. https://doi.org/10.1016/S0040-4020(01)89311-X
  8. Basavaiah, D.; Muthukumaran, K.; Sreenivasulu, B. Synthesis2000, 545.

Cited by

  1. Highly Regio- and Diastereoselective Construction of Spirocyclopenteneoxindoles through Phosphine-Catalyzed [3 + 2] Annulation of Morita–Baylis–Hillman Carbonates with Isatylidene Malononitriles vol.13, pp.13, 2011, https://doi.org/10.1021/ol201094f
  2. A cascade reaction of pyrrole-2-carbaldehyde substituted Morita–Baylis–Hillman adducts in the presence of tetrabutylammonium hydroxide or acetate to construct aza-heterocycles vol.48, pp.37, 2012, https://doi.org/10.1039/c2cc31358h
  3. Investigating the Ritter Type Reaction of α-Methylene-β-hydroxy Esters in Acidic Medium: Evidence for the Intermediacy of an Allylic Cation vol.2013, pp.23, 2013, https://doi.org/10.1002/ejoc.201300035
  4. Diels–Alder dimerization of Morita–Baylis–Hillman acetates catalyzed by organocatalysts vol.39, pp.1, 2013, https://doi.org/10.1007/s11164-012-0626-6
  5. A Practical and Stereoselective Synthesis of Cinnamyl Alcohols Bearing α-Cyano or α-Ester Functional Group from Baylis—Hillman Adducts. vol.35, pp.34, 2004, https://doi.org/10.1002/chin.200434091
  6. Synthesis of Hexahydrofuro[2,3-b]furan and Hexahydrofuro[2,3-b]pyran Derivatives Starting from Baylis-Hillman Adducts via the Ueno-Stork Reaction vol.27, pp.6, 2006, https://doi.org/10.5012/bkcs.2006.27.6.929
  7. Eschenmoser-Claisen Rearrangement of Baylis-Hillman Adducts vol.28, pp.11, 2007, https://doi.org/10.5012/bkcs.2007.28.11.2093
  8. Synthesis of Isochroman and Tetrahydroisoquinoline Derivatives from Baylis-Hillman Adducts by Radical Cyclization vol.28, pp.12, 2004, https://doi.org/10.5012/bkcs.2007.28.12.2501