Abstract
Boron Nitride (BN) efficiently catalyzes the conjugate addition of sulfur and nitrogen nucleophiles to α,β- unsaturated ketones, sulfone, phosphonate, amides, nitriles and esters under solvent-free condition in good yields at room temperature. The attributes of this protocol are operational simplicity, recyclability, high yields of products, innocuous catalyst and solvent-free condition.
Keywords: Hetero-Michael reaction, Boron Nitride, Solvent-free condition, Thiols, Amines, α, β-unsaturated compounds.
Current Catalysis
Title:Boron Nitride: An Efficient Reusable Heterogeneous Catalyst for Hetero- Michael Reactions Under Solvent-Free Condition
Volume: 2 Issue: 2
Author(s): Aniruddha Molla and Sahid Hussain
Affiliation:
Keywords: Hetero-Michael reaction, Boron Nitride, Solvent-free condition, Thiols, Amines, α, β-unsaturated compounds.
Abstract: Boron Nitride (BN) efficiently catalyzes the conjugate addition of sulfur and nitrogen nucleophiles to α,β- unsaturated ketones, sulfone, phosphonate, amides, nitriles and esters under solvent-free condition in good yields at room temperature. The attributes of this protocol are operational simplicity, recyclability, high yields of products, innocuous catalyst and solvent-free condition.
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Cite this article as:
Molla Aniruddha and Hussain Sahid, Boron Nitride: An Efficient Reusable Heterogeneous Catalyst for Hetero- Michael Reactions Under Solvent-Free Condition, Current Catalysis 2013; 2 (2) . https://dx.doi.org/10.2174/2211544711302020002
DOI https://dx.doi.org/10.2174/2211544711302020002 |
Print ISSN 2211-5447 |
Publisher Name Bentham Science Publisher |
Online ISSN 2211-5455 |
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