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December 4, 1998Angewandte Chemie International Edition157 citations

Mechanistic Insights into Cu-Catalyzed Asymmetric Aldol Reactions: Chemical and Spectroscopic Evidence for a Metalloenolate Intermediate

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BPBrian L. PagenkopfJKJochen KrügerASAleksandar Stojanovic

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Abstract

In situ IR spectroscopy and transmetalation experiments confirm a postulated catalytic cycle. The metalloenolate 1 describes the active intermediate in the aldol reaction catalyzed by CuF2 (S) -tol-binap (see reaction scheme). (S) -tol-binap= (S) - (−) -2, 2′-bis (di-p-tolylphosphanyl) -1, 1′-binaphthyl.

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Cite This Study

Pagenkopf et al. (1998) studied this question.

synapsesocial.com/papers/6a87161fb688e10ffe82c818https://doi.org/10.1002/(sici)1521-3773(19981204)37:22<3124::aid-anie3124>3.0.co;2-1
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