[[abstract]]Asymmetric reductive ring opening of oxa- and azabenzonorbornadienes with organic acids and zinc powder under mild conditions catalyzed by Ni(binap)Cl-2 or Pd(binap)l(2) produces the corresponding 1,2-dihydronaphth-1-ols in good to excellent yields with high enantioselectivity.[[fileno]]2010326010084[[department]]化學
[[abstract]]Bicyclic alkenes, including oxa- and azabenzonorbornadienes and their derivatives, can b...
Palladium-catalyzed <i>syn</i>-stereocontrolled ring-opening reactions of oxabenzonorbornadienes wit...
Asymmetric reductive cross-electrophile coupling is a powerful method to forge C–C bonds and access ...
The asymmetric ring opening reactions of bicyclic alkenes with boronic acids were accomplished by us...
grantor: University of TorontoOxabicyclo[2.2.1]heptenes were shown to undergo highly enant...
[[abstract]]A highly regio- and stereoselective ring-opening addition of alkenylzirconium reagents t...
[[abstract]]Treatment of 7-oxa- and 7-azabonzonorbornadienes with terminal acetylenes in the presenc...
An unprecedented copper phosphoramidite catalyzed enantioselective alkylative ring-opening reaction ...
An unprecedented copper phosphoramidite catalyzed enantioselective alkylative ring-opening reaction ...
A new, versatile, and highly efficient nickel-catalyzed asymmetric ring-opening (ARO) reaction of ox...
A novel iridium-catalyzed asymmetric ring-opening (ARO) reaction of oxabenzonorbornadienes with a va...
The synthesis of heterocycles using transition metal catalysis is a topic of broad interest in the f...
A new platinum(II)-catalyzed asymmetric ring-opening addition of arylboronic acids to oxabenzonorbo...
A platinum(II)-catalyzed asymmetric ring opening of oxabenzonorbornadienes with phenols was develop...
[[abstract]]7-Oxabenzonorbornadienes derivatives 1a-d underwent reductive coupling with alkyl propio...
[[abstract]]Bicyclic alkenes, including oxa- and azabenzonorbornadienes and their derivatives, can b...
Palladium-catalyzed <i>syn</i>-stereocontrolled ring-opening reactions of oxabenzonorbornadienes wit...
Asymmetric reductive cross-electrophile coupling is a powerful method to forge C–C bonds and access ...
The asymmetric ring opening reactions of bicyclic alkenes with boronic acids were accomplished by us...
grantor: University of TorontoOxabicyclo[2.2.1]heptenes were shown to undergo highly enant...
[[abstract]]A highly regio- and stereoselective ring-opening addition of alkenylzirconium reagents t...
[[abstract]]Treatment of 7-oxa- and 7-azabonzonorbornadienes with terminal acetylenes in the presenc...
An unprecedented copper phosphoramidite catalyzed enantioselective alkylative ring-opening reaction ...
An unprecedented copper phosphoramidite catalyzed enantioselective alkylative ring-opening reaction ...
A new, versatile, and highly efficient nickel-catalyzed asymmetric ring-opening (ARO) reaction of ox...
A novel iridium-catalyzed asymmetric ring-opening (ARO) reaction of oxabenzonorbornadienes with a va...
The synthesis of heterocycles using transition metal catalysis is a topic of broad interest in the f...
A new platinum(II)-catalyzed asymmetric ring-opening addition of arylboronic acids to oxabenzonorbo...
A platinum(II)-catalyzed asymmetric ring opening of oxabenzonorbornadienes with phenols was develop...
[[abstract]]7-Oxabenzonorbornadienes derivatives 1a-d underwent reductive coupling with alkyl propio...
[[abstract]]Bicyclic alkenes, including oxa- and azabenzonorbornadienes and their derivatives, can b...
Palladium-catalyzed <i>syn</i>-stereocontrolled ring-opening reactions of oxabenzonorbornadienes wit...
Asymmetric reductive cross-electrophile coupling is a powerful method to forge C–C bonds and access ...