Catalytic enantioselective epoxidation with arabinose-derived uloses containing tunable steric sensors

Tony K.M. Shing; Gulice Y.C. Leung; Kwan W. Yeung

doi:10.1016/j.tetlet.2003.09.226

Catalytic enantioselective epoxidation with arabinose-derived uloses containing tunable steric sensors

Tony K.M. Shing, Gulice Y.C. Leung, Kwan W. Yeung

化学科

研究成果: Article › 査読

35 被引用数 (Scopus)

抄録

Readily available arabinose-derived 4-uloses, containing a tunable butane-2,3-diacetal as the steric sensor, displayed increasing enantioselectivity (up to 93% ee) with the size of the acetal alkyl group in catalytic asymmetric epoxidation of trans-disubstituted and trisubstituted alkenes.

本文言語	English
ページ（範囲）	9225-9228
ページ数	4
ジャーナル	Tetrahedron Letters
巻	44
号	51
DOI	https://doi.org/10.1016/j.tetlet.2003.09.226
出版ステータス	Published - 2003 12月 15

ASJC Scopus subject areas

生化学
創薬
有機化学

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10.1016/j.tetlet.2003.09.226

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Catalytic enantioselective epoxidation with arabinose-derived uloses containing tunable steric sensors

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