Diastereoselective formation of a dicopper(i) helicate with a chiral tetradentate pyridylthiazole ligand.

Chem Commun (Camb)

Department of Biology and Chemistry, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong, China.

Published: April 2009

Reaction of a pinene-based pyridylthioamide with 1,4-dibromo-2,3-butanedione in refluxing methanol yielded a new chiral pyridylthiazole ligand L which forms a dinuclear double-stranded helicate with Cu(i) ions; this helicate has opposite helical chirality when compared with its quaterpyridine analogue.

Download full-text PDF

Source
http://dx.doi.org/10.1039/b900264bDOI Listing

Publication Analysis

Top Keywords

pyridylthiazole ligand
8
diastereoselective formation
4
formation dicopperi
4
dicopperi helicate
4
helicate chiral
4
chiral tetradentate
4
tetradentate pyridylthiazole
4
ligand reaction
4
reaction pinene-based
4
pinene-based pyridylthioamide
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!