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Efficient Synthesis of Doubly Connected Primary Face-to-Face Cyclodextrin Homo-Dimers.

✍ Scribed by Thomas Lecourt; Jean-Maurice Mallet; Pierre Sinay

Publisher: John Wiley and Sons
Year: 2004
Weight: 52 KB
Volume: 35
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200411180

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📜 SIMILAR VOLUMES

Efficient Synthesis of Doubly Connected

Efficient Synthesis of Doubly Connected Primary Face-to-Face Cyclodextrin Homo-Dimers

✍ Thomas Lecourt; Jean-Maurice Mallet; Pierre Sinaÿ 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 182 KB

## Abstract “Head‐to‐head” type α‐ and β‐cyclodextrin homo‐dimers in which the two primary rims are doubly ligated through alkyl chains have been synthesised in high yield by acyclic diene metathesis (ADM), followed by ring‐closing metathesis (RCM). (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinhe

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A useful method for the synthesis of secondary face-to-face cyclodextrin dimers retaining the glucoside form was achieved.

Symmetrical doubly connected head-to-hea

Symmetrical doubly connected head-to-head α-cyclodextrin dimers: a high yield synthesis of a novel type of neoglycolipid

✍ Thomas Lecourt; Jean-Maurice Mallet; Pierre Sinaÿ 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 148 KB

A 'head-to-head' type a-cyclodextrin dimer, wherein the two primary rims are doubly ligated through alkyl chains, is synthesised in high yield using acyclic diene metathesis (ADM) followed by ring closing metathesis (RCM).