4.8 Article

Simple preparation of diamondoid 1,3-dienes via oxetane ring opening

Journal

ORGANIC LETTERS
Volume 9, Issue 13, Pages 2541-2544

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol070920n

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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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