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Haug, B.E. and Rich, D.H. (2004) Synthesis of a Gln-Phe Hydroxy-Ethylene Dipeptide Isostere. Organic Letters, 6, 4783-4786.
https://doi.org/10.1021/ol047879y

has been cited by the following article:

• TITLE: Investigation into Protective Groups for Anilino Functionality upon Oxone-Mediated Oxidative Esterification

  AUTHORS: Tomoko Mineno, Takeya Yamamoto, Tomoya Nobuta, Hisao Kansui

  KEYWORDS: Protective Groups, Anilino Functionality, Oxone, Aldehyde, Oxidative Esterification

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.13 No.1, March 13, 2023

  ABSTRACT: In the course of organic synthesis, particularly for multi-step synthesis or natural product total synthesis, the selection of appropriate protective groups for the intended functionality is crucial in order to achieve chemoselective synthetic goals. The development of many useful protective groups has been reported based on the functionality of the anilino group. Herein, we discuss our study of various protective groups and the processes we used to establish compatibility with anilino functionality via the implementation of Oxone-mediated oxidative esterification in methanol. The results and the details of our experiments are reported herein.