@article {46322,
	title = {Diastereoselective multi-component tandem condensation: synthesis of 2-amino-4-(2-furanone)-4H-chromene-3-carbonitriles},
	journal = {Organic \& Biomolecular Chemistry},
	volume = {17},
	year = {2019},
	month = {OCT},
	pages = {8853-8857},
	type = {Article},
	abstract = {<p>A general strategy for a one-pot stereoselective synthesis of 2-amino-4-(2-furanone)-4H-chromene-3-carbonitriles by reaction of salicylaldehyde, malononitrile and butenolides via a tandem Knoevenagel/Pinner/vinylogous Michael condensation is presented. The beta,gamma-butenolides gave a syn-selective MCR adduct with a dr up to 11.5 : 1. The mechanistic insight into the MCR was obtained by DFT calculations.</p>
},
	issn = {1477-0520},
	doi = {10.1039/c9ob01345h},
	author = {Gupta, Vijay and Sahu, Debashish and Jain, Shailja and Vanka, Kumar and Singh, Ravi P.}
}
@article {47644,
	title = {Deoxygenative hydroboration of primary and secondary amides: a catalyst-free and solvent-free approach},
	journal = {Chemical Communications},
	volume = {57},
	year = {2021},
	month = {OCT },
	pages = {10596-10599},
	type = {Article},
	abstract = {In contrast to the recent reports on catalytic hydroboration of amides to amines with pinacolborane (HBpin), a simple catalyst-free and solvent-free method for the hydroboration of a variety of amides has been realized. To get the mechanistic insights, DFT calculations have been performed.},
	issn = {1359-7345},
	doi = {10.1039/d1cc04148g},
	author = {Kumar, Rohit and Bisai, Milan Kumar and Jain, Shailja and Vanka, Kumar and Sen, Sakya S.}
}
