Arabinose-derived auxiliaries in asymmetric Diels-Alder reaction

Tony Kung Ming Shing, Paul Lloyd-Williams

Research output: Contribution to journalArticle

19 Citations (Scopus)

Abstract

The readily available auxiliary alcohol, benzyl 2,3-O-isopropylidene- β-L-arabinopyranoside (1), is shown to be superior to its methyl-congener (2) in asymmetric induction capacity, attributable to a more efficient shielding by the phenyl ring.

Original languageEnglish
Pages (from-to)423-424
Number of pages2
JournalJournal of the Chemical Society, Chemical Communications
Issue number6
DOIs
Publication statusPublished - 1987 Dec 1
Externally publishedYes

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Benzyl Alcohol
Arabinose
Cycloaddition Reaction
Shielding
Alcohols
propylene

ASJC Scopus subject areas

  • Molecular Medicine

Cite this

Arabinose-derived auxiliaries in asymmetric Diels-Alder reaction. / Shing, Tony Kung Ming; Lloyd-Williams, Paul.

In: Journal of the Chemical Society, Chemical Communications, No. 6, 01.12.1987, p. 423-424.

Research output: Contribution to journalArticle

Shing, Tony Kung Ming ; Lloyd-Williams, Paul. / Arabinose-derived auxiliaries in asymmetric Diels-Alder reaction. In: Journal of the Chemical Society, Chemical Communications. 1987 ; No. 6. pp. 423-424.
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