Tetrahedron

Reactions of (Z)-3-aryl-3-chloropropenals with nucleophiles: stereoselective formation of (E)-vinylogous esters,(E)-vinylogous amides, and vinamidinium salts

…, M Hudson, E Jackson, R Miller, B Norwood, R Kanters…

Index: Clough, Stuart; Gupton, John; Ligali, Adepeju; Roberts, Matthew; Driscoll, David; Annett, Scott; Hewitt, Alisa; Hudson, Matthew; Jackson, Edward; Miller, Robert; Norwood, Bradley; Kanters, Rene; Wyre, Hadley; Petruzzi, Heather Tetrahedron, 2005 , vol. 61, # 31 p. 7554 - 7561

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Citation Number: 3

Abstract

Download PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... The highly stereoselective conversions of (Z)-3-aryl-3-chloropropenals to (E)-3-alkoxy-3-arylpropenals, to (E)-3-aryl-3-morphorlinopropenals, and to vinamidinium salts are reported. The stereochemical assignments were based on 2D-NMR experiments. ... In the course of our studies with ...

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