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Abstract Cyclic olefins were prepared via a novel synthetic approach that involves the formation of two C C bonds in a potentially stereoselective fashion. The first bond is formed by… Click to show full abstract
Abstract Cyclic olefins were prepared via a novel synthetic approach that involves the formation of two C C bonds in a potentially stereoselective fashion. The first bond is formed by employing a Mitsunobu dehydrative C-alkylation; the second C C bond involves a ring contraction via Ramberg-Backlund rearrangement.
Keywords:
olefins via;
synthesis cyclic;
cyclic olefins;
ring contraction;
alkylation
Journal Title: Tetrahedron Letters
Year Published: 2018
Link to full text (if available)
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Journal Title: Tetrahedron Letters
Year Published: 2018
Link to full text (if available)
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recommendations!