Enantioselective total synthesis of periconiasin A?
Organic Chemistry Frontiers Pub Date: 2017-12-01 DOI: 10.1039/C7QO00952F
Abstract
A concise, enantioselective total synthesis of periconiasin A, a hybrid natural product, has been achieved, featuring a ring closing metathesis (RCM) reaction and a Suzuki coupling to secure a (Z,E,E)-skipped triene system and an intramolecular Diels–Alder (IMDA) reaction to construct the challenging 6–9 fused ring system.
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Journal Name：Organic Chemistry Frontiers
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CAS no.: 89640-58-4
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