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2015 | Online First | Buchkapitel

Brønsted Acid/Lewis Base Hybrid Complexes

verfasst von : Manabu Hatano, Kazuaki Ishihara

Erschienen in: Topics in Organometallic Chemistry

Verlag: Springer International Publishing

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Abstract

Recent progress on our Brønsted acid/Lewis base hybrid complexes in some asymmetric catalyses is reviewed. Based on the rational design of conjugated acid–base catalysts, tailor-made supramolecular catalysts can show remarkable catalytic activity and higher-ordered selectivities that cannot be realized by ready-made single-molecule catalysts. The chiral supramolecular magnesium(II) binaphtholate complexes trigger the highly enantioselective 1,4-hydrophosphinylation and 1,2-hydrophosphonylation of α,β-unsaturated carbonyl compounds, direct Mannich-type reaction, and hetero-Diels–Alder reaction. Moreover, the advanced supramolecular catalysts are prepared in situ from chiral 3,3′-disubstituted binaphthols and biphenols, arylboronic acid, and B(C₆F₅)₃, for promoting the anomalous endo-/exo-selective Diels–Alder reaction. The specific mechanism and deep insights into the possible key intermediates are discussed on the basis of rational design of chiral supramolecular Brønsted acid/Lewis base hybrid catalysts as artificial enzymes.

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Titel: Brønsted Acid/Lewis Base Hybrid Complexes
verfasst von: Manabu Hatano
Kazuaki Ishihara
Verlag: Springer International Publishing
DOI: https://doi.org/10.1007/3418_2015_143

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