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Volumn 44, Issue 15, 2005, Pages 2232-2234

Remarkably stable (Me3Al)2·DABCO and stereoselective nickel-catalyzed AlR3 (R = Me, Et) additions to aldehydes

Author keywords

Aluminum; Asymmetric catalysis; Lewis bases; Nickel; Phosphoramidites

Indexed keywords

AIR; ALCOHOLS; ALDEHYDES; CATALYSIS; NICKEL; STEREOCHEMISTRY;

EID: 17644399859     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200462569     Document Type: Article
Times cited : (121)

References (26)
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    • 2} (Y = O, NR) can be of superior reactivity in some cases: c) D. Gelman, S. Dechert, H. Schumann, J. Blum, Inorg. Chim. Acta 2002, 334, 149-158; d) H. Schumann, M. Frick, B. Heymer, F. Girgsdies, J. Organomet. Chem. 1996, 512, 117-126.
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    • note
    • Individual ligand optimization is underway in our laboratory for both alkyl aldehyde and enal substrates (on the basis of PM3 studies of the selective step in the reaction).
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    • note
    • 11C(=O)Et (c = cyclo) can be detected, which indicates product racemization by Meerwin-Pondorf-Varley- Oppenauer reactions. Related ketones were not detected in the products 4.


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