Literature DB >> 14961618

A general, selective, high-yield N-demethylation procedure for tertiary amines by solid reagents in a convenient column chromatography-like setup.

Thomas Rosenau1, Andreas Hofinger, Antje Potthast, Paul Kosma.   

Abstract

[reaction: see text] A traditional preparative chromatographic column can be used to achieve quantitative N-demethylation of tertiary N-methylamines and alkaloids. The filling is the crucial part and is loaded with different solid reagents in three reaction zones. The parent compound is charged on the column, and the neat N-demethylated secondary amine leaves the column some minutes later.

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Year:  2004        PMID: 14961618     DOI: 10.1021/ol036319g

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


  4 in total

1.  Small molecule quantification by liquid chromatography-mass spectrometry for metabolites of drugs and drug candidates.

Authors:  Upendra P Dahal; Jeffrey P Jones; John A Davis; Dan A Rock
Journal:  Drug Metab Dispos       Date:  2011-09-21       Impact factor: 3.922

2.  Comparative study of the affinity and metabolism of type I and type II binding quinoline carboxamide analogues by cytochrome P450 3A4.

Authors:  Upendra P Dahal; Carolyn Joswig-Jones; Jeffrey P Jones
Journal:  J Med Chem       Date:  2011-12-01       Impact factor: 7.446

3.  Synthesis of 2,4,6-tri-substituted-1,3,5-triazines.

Authors:  Carlos A M Afonso; Nuno M T Lourenço; Andreia de A Rosatella
Journal:  Molecules       Date:  2006-01-31       Impact factor: 4.411

4.  Minimization of Back-Electron Transfer Enables the Elusive sp3 C-H Functionalization of Secondary Anilines.

Authors:  Huaibo Zhao; Daniele Leonori
Journal:  Angew Chem Int Ed Engl       Date:  2021-03-03       Impact factor: 15.336

  4 in total

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