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T. Mukaiyama H. Fujisawa and T. Nakagawa, “Lewis Base Catalyzed Aldol Reaction of Trimethylsilyl Enolates with Aldehydes,” Helvetica Chimica Acta, Vol. 85, No. 12, 2002, pp. 4518-4531.doi:10.1002/hlca.200290025

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.