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W.-H. Wang, T. Abe, X.-B. Wang, K. Kodama, T. Hirose and G.-Y. Zhang, “Self-Assembled Proline-Amino Thiou-reas as Efficient Organocatalysts for the Asymmetric Michael Addition of Al-dehydes to Nitroolefins,” Tetrahedron: Asymmetry, Vol. 21, No. 24, 2010, pp. 2925- 2933. doi:10.1016/j.tetasy.2010.11.025

has been cited by the following article:

• TITLE: Mannich-Type Reactions of Aldimines and Hetero Diels-Alder Reactions of Aldehydes Catalyzed by Anion-Type Lewis Bases Derived from a Single Molecule

  AUTHORS: Kaori Ishimaru, Daiki Maeda, Kaori Ono, Yuya Tanimura

  KEYWORDS: Anion Catalyst; Lewis Base; Proline; Mannich-Type Reaction; Hetero Diels-Alder Reaction

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.2 No.3, September 25, 2012

  ABSTRACT: Mannich-type reactions of aldimines with silyl enolates and hetero Diels-Alder reactions of aldehydes with Danishef-sky’s diene in the presence of anion catalysts derived from proline were performed to afford the corresponding products in high yields.