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Simple preparation of diamondoid 1,3-dienes via oxetane ring opening
Authors:Fokin Andrey A  Butova Ekaterina D  Chernish Lesya V  Fokina Natalie A  Dahl Jeremy E P  Carlson Robert M K  Schreiner Peter R
Institution:Department of Organic Chemistry, Kiev Polytechnic Institute, pr. Pobedy 37, 03056 Kiev, Ukraine. aaf@xtf.ntu-kpi.kiev.ua
Abstract:The transformations of apical mono- and bisacetyl diamondoids to the respective oxetanes and subsequent acid-catalyzed ring opening/dehydration lead to diamondoidyl mono- and bis-1,3-dienes in high preparative yields.
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