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Volumn 352, Issue 18, 2010, Pages 3348-3354

Trimethylchlorosilane and silicon tetrachloride in two novel methodologies for the efficient and mild aldol addition of β-keto esters and malonates to aldehydes

Author keywords

keto esters; aldol addition; malonates; silicon tetrachloride; trimethylchlorosilane

Indexed keywords


EID: 78650397752     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201000573     Document Type: Article
Times cited : (35)

References (46)
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    • A reversible cyclization of the hydroxy group with the cyano group of the aldol adduct could also explain the observed low reactivity (more details will be given in a future paper). For a recent reference about the formation of iminophthalanes and isoindolinones through a Henry reaction of o-cyanobenzaldehyde see
    • A reversible cyclization of the hydroxy group with the cyano group of the aldol adduct could also explain the observed low reactivity (more details will be given in a future paper). For a recent reference about the formation of iminophthalanes and isoindolinones through a Henry reaction of o-cyanobenzaldehyde see:, M. Angelin, M. Rahm, A. Fischer, T. Brinck, O. Ramstrom, J. Org. Chem. 2010, 75, 5882-5887.
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    • For recent applications of trimethylchlorosilane as Lewis acid see
    • For recent applications of trimethylchlorosilane as Lewis acid see


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