Volume 119, Issue 31 pp. 6005-6007
Zuschrift

Palladium-Catalyzed Asymmetric [3+3] Cycloaddition of Trimethylenemethane Derivatives with Nitrones

Ryo Shintani Dr.

Ryo Shintani Dr.

Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan, Fax: (+81) 75-753-3988

Search for more papers by this author
Soyoung Park

Soyoung Park

Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan, Fax: (+81) 75-753-3988

Search for more papers by this author
Wei-Liang Duan

Wei-Liang Duan

Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan, Fax: (+81) 75-753-3988

Search for more papers by this author
Tamio Hayashi Prof. Dr.

Tamio Hayashi Prof. Dr.

Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan, Fax: (+81) 75-753-3988

Search for more papers by this author
First published: 25 July 2007
Citations: 36

Support has been provided in part by a Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science, and Technology, Japan (21 COE on Kyoto University Alliance for Chemistry).

Graphical Abstract

Leichte Cyclisierung: Funktionalisierte 1,2-Oxazine sind durch die palladiumkatalysierte asymmetrische [3+3]-Cycloaddition zwischen Trimethylenmethan-Derivaten und Nitronen zugänglich. Der Einsatz eines modifizierten Phosphoramiditliganden liefert diese Verbindungen mit hoher Stereoselektivität (siehe Schema, Cp=Cyclopentadienyl).

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.