Literature DB >> 27083498

A Hantzsch Amido Dihydropyridine as a Transfer Hydrogenation Reagent for α,β-Unsaturated Ketones.

Scott A Van Arman1, Austin J Zimmet1, Ian E Murray1.   

Abstract

An improved synthesis of the bis-methylamido Hantzsch dihydropyridine is described. The Hantzsch amide is demonstrated to be an effective transfer hydrogenation reagent using α,β-unsaturated ketones as the test case. Unreacted Hantzsch amide and the bis-methylamidopyridine byproduct are effectively removed by extraction in contrast to the commonly used Hantzsch diethyl ester. Several examples are given with the reaction being more effective for conjugated aromatic substrates than for aliphatics.

Entities:  

Year:  2016        PMID: 27083498     DOI: 10.1021/acs.joc.6b00041

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Balancing Bulkiness in Gold(I) Phosphino-triazole Catalysis.

Authors:  Yiming Zhao; Matthew G Wakeling; Fernanda Meloni; Tze Jing Sum; Huy van Nguyen; Benjamin R Buckley; Paul W Davies; John S Fossey
Journal:  European J Org Chem       Date:  2019-07-30

2.  Chemoselective and metal-free reduction of α,β-unsaturated ketones by in situ produced benzeneselenol from O-(tert-butyl) Se-phenyl selenocarbonate.

Authors:  Andrea Temperini; Marco Ballarotto; Carlo Siciliano
Journal:  RSC Adv       Date:  2020-09-11       Impact factor: 4.036

  2 in total

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