01355nas a2200169   4500008004100000022001400041245011500055210006900170260000900239300001400248490000700262520071800269100002300987700002301010700002101033856013101054       2020                        eng d  a1359-734500aGold and hypervalent iodine(iii): liaisons over a decade for electrophilic functional group transfer reactions0 aGold and hypervalent iodineiii liaisons over a decade for electr  cMAR   a2677-26900 v563 a<p>Over the last two decades, hypervalent iodine(iii) reagents have evolved from being `bonding curiosities' to mainstream reagents in organic synthesis, in particular, electrophilic functional group transfer reactions. In this context, gold catalysts have not only emerged as a unique toolbox to facilitate such reactions (especially alkynylations) but also opened new possibilities with their different modes of reactivities for other functional group transfer reactions (acetoxylations and arylations). This feature article critically summarizes hitherto all such Au-catalyzed electrophilic functional group transfer reactions with hypervalent iodine(iii) reagents, emphasizing their mechanistic aspects.</p>
1 aBanerjee, Somsuvra1 aBhoyare, Vivek, W.1 aPatil, Nitin, T.  uhttps://library.ncl.res.in/content/gold-and-hypervalent-iodineiii-liaisons-over-decade-electrophilic-functional-group-transfer