2011
DOI: 10.1002/chin.201105118
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ChemInform Abstract: Reactions of Substituted Oxazoles and Thiazoles with Acid Chlorides: Carbon—Carbon Bond Formation Through Cyclic Ketene Acetals.

Abstract: The reaction of 2‐alkylated thiazoles and oxazoles with aryl chlorides is investigated under different conditions.

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“…This latter compound is then hydrolysed with excess alcoholic base (ii) to yield the desired enol-oxazoline product (5: Scheme 1). Materials such as 4 have found application in the production of other heterocycles [23] and as general synthetic intermediates [24][25][26][27]. A compound of general formula 4 (Scheme 1) has not previously been the subject of study via single crystal X-ray diffraction.…”
Section: Introductionmentioning
confidence: 99%
“…This latter compound is then hydrolysed with excess alcoholic base (ii) to yield the desired enol-oxazoline product (5: Scheme 1). Materials such as 4 have found application in the production of other heterocycles [23] and as general synthetic intermediates [24][25][26][27]. A compound of general formula 4 (Scheme 1) has not previously been the subject of study via single crystal X-ray diffraction.…”
Section: Introductionmentioning
confidence: 99%