Scientific article
Letter
English

Very efficient phosphoramidite ligand for asymmetric iridium-catalyzed allylic alkylation

Published inOrganic letters, vol. 6, no. 20, p. 3529-3552
Publication date2004
Abstract

Linear or branched allylic carbonates or acetates undergo enantioselective iridium-catalyzed allylic substitution with sodium malonate. The reaction is wide in scope and affords the branched product in high yield and with high regio- (up to >99:1) and enantioselectivity (up to 98%). Ten aromatic or aliphatic substrates were successfully tested.

Citation (ISO format)
ALEXAKIS, Alexandre, POLET, Damien. Very efficient phosphoramidite ligand for asymmetric iridium-catalyzed allylic alkylation. In: Organic letters, 2004, vol. 6, n° 20, p. 3529–3552. doi: 10.1021/ol048607y
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Article (Published version)
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Journal ISSN1523-7052
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