Abstract:A series of phosphorus/sulfur ligands were readily prepared and successfully applied in the Pd-catalyzed enantioselective allylic substitution and Cu-catalyzed conjugated additions of cyclic enones, respectively. The Pd-catalyzed enantioselective allylic substitution showed the best yield of 98% with 74% ee. For the Cu-catalyzed conjugated additions of cyclic enones, the best yield of 100% with 76% ee at the temperature of -30°C could be obtained.
“…The organosulfur compounds are commonly occurring in natural products and drug molecules . Among them, chiral sulfides display numerous biological activities, which also serve as indispensable intermediates in synthetic organic chemistry . Consequently, developing the protocols for C–S bond formations has attracted a great deal of interest among researchers at the forefront of investigation and innovation in modern synthetic organic chemistry.…”
An enantioselective sulfenylation of β-naphthols has been developed for the first time using a newly synthesized cinchona-derived thiourea as the catalyst and N-(arylthio) succinimide (or phthalimide) as an electrophilic sulfur source. Various enantioenriched naphthalenones with an S-containing all-substituted stereocenter were prepared via a dearomatization strategy under mild reaction conditions.
“…The organosulfur compounds are commonly occurring in natural products and drug molecules . Among them, chiral sulfides display numerous biological activities, which also serve as indispensable intermediates in synthetic organic chemistry . Consequently, developing the protocols for C–S bond formations has attracted a great deal of interest among researchers at the forefront of investigation and innovation in modern synthetic organic chemistry.…”
An enantioselective sulfenylation of β-naphthols has been developed for the first time using a newly synthesized cinchona-derived thiourea as the catalyst and N-(arylthio) succinimide (or phthalimide) as an electrophilic sulfur source. Various enantioenriched naphthalenones with an S-containing all-substituted stereocenter were prepared via a dearomatization strategy under mild reaction conditions.
New chiral-at-metal ruthenium indenyl PPh 3 phosphoramidite allenylidene complexes have been synthesized and structurally characterized. Through thermal ligand-exchange reactions with [RuCl(Ind)(PPh 3 ) 2 ], the phosphoramidite ligands
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