BiCl 3 ‐Catalyzed Hydroamination of Norbornene with Aromatic Amines | Zendy

Wei Hua | Zendy; Qian Guimin | Zendy; Xia Yuanzhi | Zendy; Li Kai | Zendy; Li Yahong | Zendy; Li Wu | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

BiCl 3 ‐Catalyzed Hydroamination of Norbornene with Aromatic Amines

Author(s) -

Wei Hua,

Qian Guimin,

Xia Yuanzhi,

Li Kai,

Li Yahong,

Li Wu

Publication year - 2007

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.200700483

Subject(s) - hydroamination , chemistry , norbornene , catalysis , intermolecular force , organic chemistry , lewis acids and bases , combinatorial chemistry , molecule , copolymer , polymer

A BiCl 3 ‐catalyzed hydroamination reaction of norbornene, in which a variety of electron‐withdrawing groups were tolerated on amines, was presented. The current transformation possesses the advantages of being highly selective, cheap, and eco‐friendly, and this process also represents a rare system for main‐group Lewis acid catalyzed intermolecular hydroamination of unactivated alkenes.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research