A Simple, One‐Step Procedure for the Formation of Chiral Metallamacrocycles | Zendy

Campbell Katie | Zendy; Johnson Charles A. | Zendy; McDonald Robert | Zendy; Ferguson Michael J. | Zendy; Haley Michael M. | Zendy; Tykwinski Rik R. | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

A Simple, One‐Step Procedure for the Formation of Chiral Metallamacrocycles

Author(s) -

Campbell Katie,

Johnson Charles A.,

McDonald Robert,

Ferguson Michael J.,

Haley Michael M.,

Tykwinski Rik R.

Publication year - 2004

Publication title -

angewandte chemie international edition

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 5.831

H-Index - 550

eISSN - 1521-3773

pISSN - 1433-7851

DOI - 10.1002/anie.200461139

Subject(s) - acetylide , platinum , yield (engineering) , chemistry , one step , simple (philosophy) , conjugated system , twist , ligand (biochemistry) , combinatorial chemistry , two step , stereochemistry , computational chemistry , mathematics , materials science , organic chemistry , chemical engineering , catalysis , geometry , engineering , metallurgy , philosophy , polymer , epistemology , receptor , biochemistry

A twist in the final stage : Chiral, conjugated metallamacrocycles can be formed in excellent yield in a single step from achiral precursors by ligand exchange between ( R , R )‐ or ( S , S )‐chiraphos and trans platinum acetylide complexes (see scheme).

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research