Literature DB >> 15932198

A tuneable method for N-debenzylation of benzylamino alcohols.

Elizabeth J Grayson1, Benjamin G Davis.   

Abstract

[reactions: see text] N-Iodosuccinimide provides a mild, convenient, and tuneable reagent for the selective mono- or didebenzylation in representative, multifunctionalized carbohydrate and amino acid derived N-dibenzylamines with neighboring O-functionality.

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Year:  2005        PMID： 15932198     DOI： 10.1021/ol050624f

Source DB:  PubMed          Journal:  Org Lett        ISSN： 1523-7052            Impact factor:   6.005


  3 in total

1.  Umpolung reactivity in amide and peptide synthesis.

Authors:  Bo Shen; Dawn M Makley; Jeffrey N Johnston
Journal:  Nature       Date:  2010-06-24       Impact factor: 49.962

2.  Facile Hydrogenative Deprotection of N-Benzyl Groups Using a Mixed Catalyst of Palladium and Niobic Acid-on-Carbon.

Authors:  Yuta Yamamoto; Eisho Shimizu; Kazuho Ban; Yoshiyuki Wada; Tomoteru Mizusaki; Masatoshi Yoshimura; Yukio Takagi; Yoshinari Sawama; Hironao Sajiki
Journal:  ACS Omega       Date:  2020-02-05

3.  Synthesis of Azido-Globo H Analogs for Immunogenicity Evaluation.

Authors:  Chiang-Yun Chen; Yu-Wei Lin; Szu-Wen Wang; Yung-Chu Lin; Yang-Yu Cheng; Chien-Tai Ren; Chi-Huey Wong; Chung-Yi Wu
Journal:  ACS Cent Sci       Date:  2021-12-21       Impact factor: 14.553
  3 in total

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