A novel tandem metal-free oxidative aryl migration/C–C bond-cleavage reaction, mediated by hypervalent iodine reagent, has been discovered. The presented transformation provided straightforward access to important α-ketoamide and α-ketoester derivatives from readily available acrylic derivatives via a concerted process of 1,2-aryl shift concomitant with C–C bond cleavage
An efficient and chemoselective C(sp2)–N bond cleavage of aromatic imidazo[1,2-a]pyridine molecul...
A flexible metal-free cascade reaction involving aerobic C(sp3)–H hydroxylation and decarbonylation ...
The chemistry of hypervalent iodine(III) reagents have widely been explored in many organic transfor...
A stereoselective hypervalent iodine-promoted oxidative rearrangement of 1,1-disubstituted alkenes h...
The synthesis of α‐substituted carbonyl compounds is of great importance due to their ubiquity in bo...
An umpolung approach to amides via hypervalent iodine-mediated oxidative rearrangement of N–H ketimi...
Sequential exposure of a zinc-organometallic intermediate, generated through a zinc carbenoid-mediat...
Neutral electrophilic iodine(I) species proved to be efficient reagents for C-X bond cleavage of var...
Giving the metal the boot: The title reaction provides facile access to functionalized chiral ketone...
The α-ketoamide motif is widely found in many natural products and drug candidates with relevant bi...
© 2022 American Chemical Society.Catalytic carbon-nitrogen bond formation in hydrocarbons is an appe...
A metal-free oxidative coupling of methyl ketones and primary or secondary amines to α-ketoamides ha...
Carbonyl-containing oxindoles can be prepared from <i>N</i>-arylacrylamides and α-diketones by TBHP-...
An iodine-catalyzed oxidative cross-coupling of C–H/N–H has been demonstrated. This simple and effic...
Selectfluor-mediated simultaneous cleavage of C–O and C–C bonds in α,β-epoxy ketones has been succes...
An efficient and chemoselective C(sp2)–N bond cleavage of aromatic imidazo[1,2-a]pyridine molecul...
A flexible metal-free cascade reaction involving aerobic C(sp3)–H hydroxylation and decarbonylation ...
The chemistry of hypervalent iodine(III) reagents have widely been explored in many organic transfor...
A stereoselective hypervalent iodine-promoted oxidative rearrangement of 1,1-disubstituted alkenes h...
The synthesis of α‐substituted carbonyl compounds is of great importance due to their ubiquity in bo...
An umpolung approach to amides via hypervalent iodine-mediated oxidative rearrangement of N–H ketimi...
Sequential exposure of a zinc-organometallic intermediate, generated through a zinc carbenoid-mediat...
Neutral electrophilic iodine(I) species proved to be efficient reagents for C-X bond cleavage of var...
Giving the metal the boot: The title reaction provides facile access to functionalized chiral ketone...
The α-ketoamide motif is widely found in many natural products and drug candidates with relevant bi...
© 2022 American Chemical Society.Catalytic carbon-nitrogen bond formation in hydrocarbons is an appe...
A metal-free oxidative coupling of methyl ketones and primary or secondary amines to α-ketoamides ha...
Carbonyl-containing oxindoles can be prepared from <i>N</i>-arylacrylamides and α-diketones by TBHP-...
An iodine-catalyzed oxidative cross-coupling of C–H/N–H has been demonstrated. This simple and effic...
Selectfluor-mediated simultaneous cleavage of C–O and C–C bonds in α,β-epoxy ketones has been succes...
An efficient and chemoselective C(sp2)–N bond cleavage of aromatic imidazo[1,2-a]pyridine molecul...
A flexible metal-free cascade reaction involving aerobic C(sp3)–H hydroxylation and decarbonylation ...
The chemistry of hypervalent iodine(III) reagents have widely been explored in many organic transfor...