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Abstract Organic azides have found wide application in various fields of science and technology. This review summarizes recently developed approaches to the direct, one‐step synthesis of diverse organic azides utilizing hypervalent iodine reagents. The first part of review deals with the azidation using unstable azidoiodinanes generatedin situfrom common hypervalent iodine reagents (such as diacetoxyiodobenzene or iodosylbenzene) and a source of azide anion (TMSN₃or NaN₃). The second part of review is dedicated to the application of stable azidobenziodoxoles as useful azidating reagents that allow selective direct azidation of C−H bonds or double carbon‐carbon bonds under mild reaction conditions. The use of azidobenziodoxoles eliminates the main disadvantages of the traditional approaches to organic azides, such as the need in pre‐functionalization of organic substrates and harsh reaction conditions. Synthetic application of azidobenziodoxoles made possible direct selective azidation of a plethora of organic substrates including complex molecules at the late synthetic stage. 

A facile metal‐free [2,3]‐sigmatropic rearrangement reaction of allyl sulfides viaN‐sulfilimine intermediates has been developed. Treatment of allyl sulfides with imino‐λ³‐iodanes in the presence of a catalytic amount of elemental iodine allowed the reaction to proceed under mild conditions and gave the correspondingN‐allylsulfenamide compounds in moderate to good yields. SeveralN‐allylsulfenamide structures have been confirmed by single‐crystal X‐ray crystallography. The reaction initially involves the sulfonylimino group transfer reaction between imino‐λ³‐iodane and the sulfur atom, resulting in the formation ofN‐sulfilimine species, followed by [2,3]‐sigmatropic rearrangement to form theN‐allylsulfenamide.