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Cardillo, G., Oren, M., Romero, M. and Sandri, S. (1989) Enantioselective Synthesis of 2-Benzyloxy Alcohols and 1, 2-Diols via Alkylation of Chiral Glycolate Imides. A Convenient Approach to Optically Active Glycerol Derivatives. Tetrahedron, 45, 1501-1508.
https://doi.org/10.1016/0040-4020(89)80148-6

has been cited by the following article:

• TITLE: Larger Scale Photochemical Bromination of Toluene, 1-Methylnaphthalene and Acetophenone in Aqueous Biphasic System and Applications of the Crude Products in Synthesis

  AUTHORS: Karolayne Kelyn de Moura Lira, Hitala Nicole Lima dos Santos, Alexander Y. Nazarenko, Edmilson Clarindo de Siqueira, Bogdan Doboszewski

  KEYWORDS: Alkylation, Anticancer, Photochemical Bromination, Phase Transfer Catalysis

  JOURNAL NAME: Open Access Library Journal, Vol.12 No.2, February 27, 2025

  ABSTRACT: Photochemical bromination of toluene up to 300 mmol per run in aqueous biphasic system formed benzyl bromide of sufficient purity to be used directly for benzylations without any purification. 1-Methylnaphthalene and acetophenone react similarly. An approach to (R) and (S) 1-O-triphenylmethyl-glycerol is presented based on L- and D-xylose.