1,2-Bis(alkynyl)benzene derivatives react with strongly electrophilic boranes to yield in boryl-functionalized bulky naphthalene derivatives by means of a sequence of 1,1-carboboration reactions. These substrates can be functionalized by transition metal catalyzed cross-coupling reactions
A series of functionalized 1-amino-2-naphthalenecarboxylic acid derivatives were synthesized from en...
ABSTRACT: Conditions have been developed for the palladium-catalyzed cross-coupling of 3-bromo-2,1-b...
Carboboration of alkynes was found to take place efficiently by a three-component coupling reaction ...
1,2-Bis(alkynyl)benzene derivatives react with strongly electrophilic boranes to yield in boryl-func...
The complexes IPrMCl (IPr = 1,3-bis(diisopropylphenyl)imidazol-2-ylidene, M = Cu, 1a; M = Au, 1b) in...
Carboranes are boron-rich molecules that can be functionalized through metal-catalyzed cross-couplin...
We reveal here the regioselective nucleophilic addition of C(sp3) to 1,1-arylboryl alkenes, followed...
During the past decade, many research groups have described catalytic methods for 1,2‐carboboration,...
A method for transition metal-free 1,2-carboboration of unactivated alkenes with bis(catecholato)d...
1,2 and 2,3-disubstituted naphthalenes were synthesized by carbene addition to substituted indenes. ...
The complexes IPrMCl (IPr = 1,3-bis(diisopropylphenyl)imidazol-2-ylidene, M = Cu, 1a; M = Au, 1b), i...
Sodium dispersion promotes the reductive borylation of polycyclic aromatic hydrocarbons (PAHs) with ...
Benzylic functionalization is a convenient approach towards the conversion of readily available arom...
Benzylic functionalization is a convenient approach towards the conversion of readily available arom...
This work showcases the 1,3‐haloboration reaction of alkynes in which boron and chlorine add to prop...
A series of functionalized 1-amino-2-naphthalenecarboxylic acid derivatives were synthesized from en...
ABSTRACT: Conditions have been developed for the palladium-catalyzed cross-coupling of 3-bromo-2,1-b...
Carboboration of alkynes was found to take place efficiently by a three-component coupling reaction ...
1,2-Bis(alkynyl)benzene derivatives react with strongly electrophilic boranes to yield in boryl-func...
The complexes IPrMCl (IPr = 1,3-bis(diisopropylphenyl)imidazol-2-ylidene, M = Cu, 1a; M = Au, 1b) in...
Carboranes are boron-rich molecules that can be functionalized through metal-catalyzed cross-couplin...
We reveal here the regioselective nucleophilic addition of C(sp3) to 1,1-arylboryl alkenes, followed...
During the past decade, many research groups have described catalytic methods for 1,2‐carboboration,...
A method for transition metal-free 1,2-carboboration of unactivated alkenes with bis(catecholato)d...
1,2 and 2,3-disubstituted naphthalenes were synthesized by carbene addition to substituted indenes. ...
The complexes IPrMCl (IPr = 1,3-bis(diisopropylphenyl)imidazol-2-ylidene, M = Cu, 1a; M = Au, 1b), i...
Sodium dispersion promotes the reductive borylation of polycyclic aromatic hydrocarbons (PAHs) with ...
Benzylic functionalization is a convenient approach towards the conversion of readily available arom...
Benzylic functionalization is a convenient approach towards the conversion of readily available arom...
This work showcases the 1,3‐haloboration reaction of alkynes in which boron and chlorine add to prop...
A series of functionalized 1-amino-2-naphthalenecarboxylic acid derivatives were synthesized from en...
ABSTRACT: Conditions have been developed for the palladium-catalyzed cross-coupling of 3-bromo-2,1-b...
Carboboration of alkynes was found to take place efficiently by a three-component coupling reaction ...