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ChemInform Abstract: Synthesis of Chiral Thiazoline Ligands Tethered to a Sulfur Function and First Immobilization of a Thiazoline-Ligand.

✍ Scribed by Isabelle Abrunhosa-Thomas; Alexander Betz; Mickael Denance; Isabelle Dez; Annie-Claude Gaumont; Mihaela Gulea

Publisher: John Wiley and Sons
Year: 2010
Weight: 23 KB
Volume: 41
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.201039031

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Synthesis of chiral thiazoline ligands t

Synthesis of chiral thiazoline ligands tethered to a sulfur function and first immobilization of a thiazoline-ligand

✍ Isabelle Abrunhosa-Thomas; Alexander Betz; Mickael Denancé; Isabelle Dez; Annie- 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 304 KB

## Abstract A new family of thiazoline ligands tethered to a sulfanyl or a sulfinyl group has been prepared using short and efficient reaction sequences. Among the different structures, one sulfanyl‐thiazoline homopolymer was synthesized as a first example of an immobilized thiazoline ligand. The c

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A Convenient Synthesis of Chiral Sulfur-Containing Macrocyclic Ligands. -A series of new optically pure sulfur-containing macrocycles (V) (8 examples), which can be used in chiral recognition, is synthesized starting from L-cysteine (I). -(LI, X.;

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v