Mild and Efficient Solvent‐Free Friedel–Crafts Acylation of Reserpine
Author:
Affiliation:
1. a H.E.J. Research Institute of Chemistry, International Center for Chemical Sciences , University of Karachi , Karachi, Pakistan
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397910600908900
Reference19 articles.
1. Organic synthesis under solvent-free condition: An environmentally benign procedure — I
2. Solid Phase Synthesis
3. Waste-free solid-state syntheses with quantitative yield
4. 1986. Vogel's Textbook of Practical Organic Chemistry, 4th ed. 770–774. Essex: ELBS/Longman.
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1. Mechanochemical Friedel–Crafts acylations;Beilstein Journal of Organic Chemistry;2019-06-17
2. A simplified synthesis of 2-acetyl-1,4,5,8-tetramethoxynaphthalene and its selective demethylation product;Russian Journal of General Chemistry;2016-12
3. Antimycobacterial and antioxidant activities of reserpine and its derivatives;Natural Product Research;2012-01-25
4. Friedel-Crafts Acylation;Comprehensive Organic Name Reactions and Reagents;2010-09-15
5. Mild and Efficient Solvent-Free Friedel—Crafts Acylation of Reserpine.;ChemInform;2007-03-13
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