Chinese Journal of Organic Chemistry >
Synthetic Studies toward Natural Occurred Cyanolide A and Cocosolide
Received date: 2019-04-29
Online published: 2019-07-09
Supported by
the National Natural Science Foundation of China(21302129);the Natural Science Foundation of Zhejiang Province(LQ13B020002)
Cyanolide A and cocosolide, two 16-membered dimeric macrolide xylopyranosides, were isolated from Guam and Papua New Guinea, respectively. Their fascinating structures and outstanding biological activities had attracted great attentions from chemists. The synthesis of cyanolide A and cocosolide is reviewed based on the construction methods of tetrahydropyran ring, which involves oxo-Michael addition reaction, oxo-carbenium cyclization and transition-metal catalyzed cyclization reactions.
Liu Zhang , Mengfan Zhang , Chenze Qi , Zhen Yang . Synthetic Studies toward Natural Occurred Cyanolide A and Cocosolide[J]. Chinese Journal of Organic Chemistry, 2019 , 39(11) : 3105 -3113 . DOI: 10.6023/cjoc201904071
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