A metal-free oxidative C(sp<sup>3</sup>)–H bond functionalization and subsequent conjugate addition reaction using di<i>-tert</i>-butyl peroxide (DTBP) as the oxidant was established, which tolerates a wide range of simple alkane substrates to react with different substituted chromones for direct preparation of 2-alkylchromanones
Carbonyl-containing oxindoles can be prepared from <i>N</i>-arylacrylamides and α-diketones by TBHP-...
A catalyst-free oxyboration reaction of alkynes is developed. The resulting borylated isocoumarins ...
A general alkylating method using organoboronic acid under 1 atm of oxygen is developed. It allows a...
The development of novel and efficient methods for the transition metal-free functionalization of in...
A DTBP-promoted oxidative functionalization of a C(sp<sup>3</sup>)–H bond adjacent to oxygen and in...
A general and metal-free radical route to synthesis of 3-acylspiro[4,5]trienones is established th...
A practical and efficient method for the synthesis of functionalized 4-(aryl-/heteroaryl-ethynyl)chr...
A metal-free CH–CH-type coupling of arenes and alkynes, mediated by a multifunctional sulfoxide dire...
A di-<i>tert</i> butyl peroxide (DTBP)-promoted α-alkylation of α-amino carbonyl compounds by simple...
A base-mediated aerobic oxidation of the C–H bond adjacent to the N-atom of a secondary amine to for...
C-3 alkylation of coumarins has been accomplished using cycloalkanes or alkylbenzenes in the presenc...
An efficient metal free oxidative esterification of sp3 C–H bonds (adjacent to an oxygen atom) in si...
The oxidation of alkanes into valuable chemical products is a vital reaction in organic synthesis. T...
For decades, synthetic organic chemists have constructed organic molecules by manipulating functiona...
A transition-metal-free oxidative coupling of allylic C-H and heterocyclic/aromatic N-H bonds was pe...
Carbonyl-containing oxindoles can be prepared from <i>N</i>-arylacrylamides and α-diketones by TBHP-...
A catalyst-free oxyboration reaction of alkynes is developed. The resulting borylated isocoumarins ...
A general alkylating method using organoboronic acid under 1 atm of oxygen is developed. It allows a...
The development of novel and efficient methods for the transition metal-free functionalization of in...
A DTBP-promoted oxidative functionalization of a C(sp<sup>3</sup>)–H bond adjacent to oxygen and in...
A general and metal-free radical route to synthesis of 3-acylspiro[4,5]trienones is established th...
A practical and efficient method for the synthesis of functionalized 4-(aryl-/heteroaryl-ethynyl)chr...
A metal-free CH–CH-type coupling of arenes and alkynes, mediated by a multifunctional sulfoxide dire...
A di-<i>tert</i> butyl peroxide (DTBP)-promoted α-alkylation of α-amino carbonyl compounds by simple...
A base-mediated aerobic oxidation of the C–H bond adjacent to the N-atom of a secondary amine to for...
C-3 alkylation of coumarins has been accomplished using cycloalkanes or alkylbenzenes in the presenc...
An efficient metal free oxidative esterification of sp3 C–H bonds (adjacent to an oxygen atom) in si...
The oxidation of alkanes into valuable chemical products is a vital reaction in organic synthesis. T...
For decades, synthetic organic chemists have constructed organic molecules by manipulating functiona...
A transition-metal-free oxidative coupling of allylic C-H and heterocyclic/aromatic N-H bonds was pe...
Carbonyl-containing oxindoles can be prepared from <i>N</i>-arylacrylamides and α-diketones by TBHP-...
A catalyst-free oxyboration reaction of alkynes is developed. The resulting borylated isocoumarins ...
A general alkylating method using organoboronic acid under 1 atm of oxygen is developed. It allows a...