Enantioselective total synthesis of periconiasin A†,Organic Chemistry Frontiers

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Enantioselective total synthesis of periconiasin A†
Organic Chemistry Frontiers ( IF 4.6 ) Pub Date : 2017-12-01 00:00:00 , DOI: 10.1039/c7qo00952f
Zhixiong Zeng _{1,

2,

3,

4,

5} , Cheng Chen _{1,

2,

3,

4,

5} , Yandong Zhang _{1,

2,

3,

4,

5}

Affiliation

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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