Cyclopropane Structural Units from Homoaldol Adducts

An efficient two-step homologation of aldehydes to cyclopropylaldehydes has been developed. Activation of homoaldol adducts derived from O-enecarbamates and N-enecarbamates provided high yields of cyclopropylaldehydes with good to excellent levels of trans/cis selectivity. Trapping of the intermedia...

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Veröffentlicht in:Organic letters 2003-04, Vol.5 (8), p.1377-1379
Hauptverfasser: Taylor, Richard E, Risatti, Christina A, Engelhardt, F. Conrad, Schmitt, Michael J
Format: Artikel
Sprache:eng
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Zusammenfassung:An efficient two-step homologation of aldehydes to cyclopropylaldehydes has been developed. Activation of homoaldol adducts derived from O-enecarbamates and N-enecarbamates provided high yields of cyclopropylaldehydes with good to excellent levels of trans/cis selectivity. Trapping of the intermediate oxonium ion and iminium ion intermediates has also been demonstrated, leading to direct isolation of cyclopropyl carbinol and cyclopropylamine products.
ISSN:1523-7060
1523-7052
DOI:10.1021/ol034448r