@article { ISI:000284533700013,
	title = {Regiospecific azidoiodination of alkenes with sodium periodate, potassium iodide, and sodium azide: a high-yield synthesis of beta-iodoazides},
	journal = {Synthesis-Stuttgart},
	number = {22},
	year = {2010},
	month = {NOV},
	pages = {3879-3882},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>The combination of sodium periodate, potassium iodide, and sodium azide has been found to be an efficient, simple, and inexpensive reagent system for azidoiodination of alkenes. The regiospecific 1,2-azidoiodination proceeds in an anti-Markovnikov fashion to produce beta-iodoazides in excellent yields.</p>},
	keywords = {alkenes, azides, azidoiodination, beta-iodoazides, regio-specific},
	issn = {0039-7881},
	doi = {10.1055/s-0030-1258250},
	author = {Chouthaiwale, Pandurang V. and Karabal, Pratibha U. and Suryavanshi, Gurunath and Sudalai, Arumugam}
}
@article {46607,
	title = {Radical rearrangement of aryl/alkylidene malononitriles via aza michael addition/decynoformylation/addition sequence: an access to alpha-aminonitriles and alpha-aminoamides},
	journal = {Journal of Organic Chemistry},
	volume = {85},
	year = {2020},
	month = {DEC },
	pages = {14858-14865},
	type = {Article},
	abstract = {<p>An efficient, safe, and environmentally friendly tertiary butyl hydrogen peroxide (TBHP)-mediated rearrangement of aryl/alkylidene malononitrile with anilines has been developed with in situ generation of HCN as the cyanide source for the synthesis of substituted alpha-aminonitriles and alpha-aminoamide. A diverse set of alpha-aminonitriles and alpha-aminoamides was efficiently synthesized in good to excellent yields. This method features a broad substrate scope and good functional group tolerance, and the in situ-generated HCN bypasses the use of an external cyanide source.</p>
},
	issn = {0022-3263},
	doi = {10.1021/acs.joc.0c01358},
	author = {Bhoite, Shubhangi P. and Bansodes, Ajay H. and Suryavanshi, Gurunath}
}
