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U. Bhoga, “A New Synthetic Approach to Enantiomerically Enriched Dihydro-benzofurans: Use of a Hydrolytic Kinetic Resolution and an Intramolecular Epoxide Ring Opening Protocol Using 1-Benzyloxy-2-oxiranylmethy- lbenzenes,” Tetrahedron Letters, Vol. 46, No. 31, 2005, pp. 5239-5242. doi:10.1016/j.tetlet.2005.04.120

has been cited by the following article:

• TITLE: Stereoselective Synthesis of cis-Substituted-3’-anilino-2’, 3’-dihydro-4-2’-benzo[b]furanylcoumarins via Intramolecular Aldol Reactions

  AUTHORS: Lokesh A. Shastri, Samundeeswari L. Shastri, Manohar V. Kulkarni, Vivek K. Gupta, Sanjeev Goswami

  KEYWORDS: Aldol Reaction; Stereoselective; Intramolecular; Mild Base; 4-Bromomethylcoumarins; Dihydrobenzofurans

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.2 No.1, March 15, 2012

  ABSTRACT: The present study reports the reaction of 4-bromomethylcoumarins with salicylidineaniline in acetone with two equivalents of potassium carbonate resulted in the formation of title compounds at room temperature via intramolecular aldolization. The obtained compound is thermodynamically and kinetically stable with highly stereoselective and excellent yield.