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ChemInform Abstract: A [4 + 2] Cycloaddition Strategy to Pyridine Boronic Ester Derivatives.

✍ Scribed by Patrick M. Delaney; Jianhui Huang; Simon J. F. Macdonald; Joseph P. A. Harrity

Publisher
John Wiley and Sons
Year
2008
Weight
44 KB
Volume
39
Category
Article
ISSN
0931-7597

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✦ Synopsis

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable via the β€œReferences” option.

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An Alkynylboronate Cycloaddition Strategy to Functionalized Benzyne Derivatives. -The cycloaddition of 2-pyrones with alkynylboronate (II) followed by C-B bond oxidation and a subsequent triflation gives rise to mixtures of regioisomers (VI) and (VII), which are shown to be useful benzyne precursors