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

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

Chemical communications (Cambridge, England) (2009-04-01)
Chui-Shan Tsang, Ho-Lun Yeung, Wing-Tak Wong, Hoi-Lun Kwong
摘要

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.

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Sigma-Aldrich
1,4-二溴-2,3-丁二酮, 99%