E-mail

E-mail a Wiley Online Library Link

Norifumi Sakiyama, Daiki Hojo, Prof. Dr. Keiichi Noguchi and Prof. Dr. Ken Tanaka Enantioselective Synthesis of Axially Chiral 1-Arylisoquinolines by Rhodium-Catalyzed [2+2+2] Cycloaddition Chemistry - A European Journal 17

Article first published online: 5 JAN 2011 | DOI: 10.1002/chem.201003134

Thumbnail image of graphical abstract

It's all in the application! An enantioselective synthesis of axially chiral 1-arylisoquinolines has been achieved, which involves a rhodium-catalyzed [2+2+2] cycloaddition of diphenylphosphinoyl-substituted 1-arylisoquinolines (see scheme). The new diphenylphosphinoyl-substituted axially chiral 1-arylisoquinolines were successfully derivatized to the corresponding axially chiral P,N ligand and Lewis base catalyst.

Complete the form below and we will send an e-mail message containing a link to the selected article on your behalf

Required = Required Field

SEARCH