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ChemInform Abstract: Synthetic Studies of Lepranthin, a Lichen-Produced Dimeric Macrolide. Stereoselective Synthesis of a seco-Acid Based on Stereospecific Epoxide-Opening Reactions.

✍ Scribed by Hisashi Takada; Shinji Nagumo; Eiko Yasui; Megumi Mizukami; Masaaki Miyashita

Publisher
John Wiley and Sons
Year
2011
Weight
21 KB
Volume
42
Category
Article
ISSN
0931-7597

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ChemInform Abstract: Synthetic Studies o
ChemInform Abstract: Synthetic Studies of the Lichen Macrolide Lepranthin. Stereoselective Synthesis of the Diolide Framework Based on Regioselective Epoxide-Opening Reactions.
✍ Hisashi Takada; Shinji Nagumo; Eiko Yasui; Megumi Mizukami; Masaaki Miyashita πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons βš– 40 KB πŸ‘ 1 views

## Abstract A synthetic approach toward 16‐membered diolide (VIIb), a fully functionalized congener of Lepranthin (VIIa), is developed.