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NMR determination of absolute configuration of α-acyloxy ketones

✍ Scribed by Jean-Christophe Jullian; Xavier Franck; Shamil Latypov; Reynald Hocquemiller; Bruno Figadère


Book ID
104359748
Publisher
Elsevier Science
Year
2003
Tongue
English
Weight
206 KB
Volume
14
Category
Article
ISSN
0957-4166

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✦ Synopsis


Determination of the absolute configuration of several acyclic a-acyloxy-ketones, and d-ketobutanolides, in the presence of a chiral solvating agent, by low temperature and low concentration 1 H NMR analysis, is reported.


📜 SIMILAR VOLUMES


NMR determination of the absolute config
✍ Hiroki Fukui; Yukiharu Fukushi; Satoshi Tahara 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 217 KB

By the use of a new axially chiral reagent, 2'-methoxy-l,l'-binaphthalene-2-carbohydroximoyl chloride (MBCC), chiral cyclic alkenes were stereoselectively derivatized into 4,5-dihydroisoxazoles. NOEs were observed between the protons of the reagent moiety and those of the alkene moiety in cycloadduc