H. Suga, T. Arikawa, K. Itoh, Y. Okumura, A. Kakehi and M. Shiro, “Asymmetric 1,3-Dipolar Cycloaddition Reactions of Azomethine Imines with Acrolein Catalyzed by L-Proline and Its Derivatives,” Heterocycles, Vol. 81, No. 7, 2010, pp. 1669-1688. doi:10.3987/COM-10-11967

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.