6.2. Synthesis of the Antitumoral Drug 2,4,6-Tris(dimethylamino)-1,3,5-triazine <i>via</i> Sequential Nucleophilic Substitution-Reference-Cited by-同舟云学术

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6.2. Synthesis of the Antitumoral Drug 2,4,6-Tris(dimethylamino)-1,3,5-triazine via Sequential Nucleophilic Substitution

Published:2016-12-16 Issue: Volume: Page:535-538
ISSN:
Container-title:Comprehensive Organic Chemistry Experiments for the Laboratory Classroom
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Author:

Siopa Filipa¹,Candeias Nuno²,Afonso Carlos A. M.¹

Affiliation:

1. Instituto de Investigação, do Medicamento (iMed.ULisboa), Faculdade de Farmácia, Universidade de Lisboa Av. Prof. Gama Pinto 1649-003 Lisboa Portugal filipasiopa@ff.ul.pt nuno.rafaelcandeias@tut.fi

2. Department of Chemistry and Bioengineering, Tampere University of Technology Korkeakoulunkatu 8 Tampere FI-33101 Finland carlosafonso@ff.ul.pt

Publisher

The Royal Society of Chemistry

Link

https://books.rsc.org/books/edited-volume/chapter-pdf/1688026/bk9781849739634-00535.pdf

Reference14 articles.

1. Recent applications of 2,4,6-trichloro-1,3,5-triazine and its derivatives in organic synthesis

2. Melamine Derivatives - A Review on Synthesis and Application

3. Synthesis of 2,4,6-Tri-substituted-1,3,5-Triazines

4. Recent Developments in the Synthesis of Bioactive 2,4,6-Trisubstituted 1,3,5-Triazines

5. Solvent-free synthesis of melamines under microwave irradiation

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