Enantioselective oxidative boron Heck reactions

Research output: Contribution to journalLiterature review

Abstract

This review highlights the use of the oxidative boron Heck reaction in enantioselective Heck-type couplings. The enantioselective oxidative boron Heck reaction overcomes several limitations of the traditional Pd(0)-catalysed Heck coupling and has subsequently allowed for intermolecular couplings of challenging systems such as cyclic enones, acyclic alkenes, and even site selectively on remote alkenes.
Original languageEnglish
Pages (from-to)5357-5366
Number of pages10
JournalOrganic and Biomolecular Chemistry
Volume14
Issue number24
Early online date29 Oct 2015
DOIs
Publication statusPublished - 28 Jun 2016

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title = "Enantioselective oxidative boron Heck reactions",
abstract = "This review highlights the use of the oxidative boron Heck reaction in enantioselective Heck-type couplings. The enantioselective oxidative boron Heck reaction overcomes several limitations of the traditional Pd(0)-catalysed Heck coupling and has subsequently allowed for intermolecular couplings of challenging systems such as cyclic enones, acyclic alkenes, and even site selectively on remote alkenes.",
author = "Ai-Lan Lee",
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publisher = "Royal Society of Chemistry",
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Enantioselective oxidative boron Heck reactions. / Lee, Ai-Lan.

In: Organic and Biomolecular Chemistry, Vol. 14, No. 24, 28.06.2016, p. 5357-5366.

Research output: Contribution to journalLiterature review

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AB - This review highlights the use of the oxidative boron Heck reaction in enantioselective Heck-type couplings. The enantioselective oxidative boron Heck reaction overcomes several limitations of the traditional Pd(0)-catalysed Heck coupling and has subsequently allowed for intermolecular couplings of challenging systems such as cyclic enones, acyclic alkenes, and even site selectively on remote alkenes.

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