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- W2019950616 abstract "Hypervalent iodine (III) reagents nowadays are used extensively in the field of organic chemistry. Especially, phenyliodine (III) diacetate (PIDA) or phenyliodine (III) bis(trifluoroacetate) (PIFA) have received much attention because of their reactivities similar to heavy metal reagents or anodic oxidation, low toxicity, ready availability and easy handling. In the continuous study of our oxidative phenolic coupling reactions using a hypervalent iodine (III) reagents, a versatile synthetic procedure for the galanthamine-type Amaryllidaceae alkaloids was accomplished. The first total synthesis of (+/-)-sanguinine and the total syntheses of (+/-)-galanthamine, (+/-)-narwedine, (+/-)-lycoramine, and (+/-)-norgalanthamine were also successfully carried out." @default.
- W2019950616 created "2016-06-24" @default.
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- W2019950616 date "2001-02-06" @default.
- W2019950616 modified "2023-09-27" @default.
- W2019950616 title "ChemInform Abstract: Development of Intramolecular Oxidative Phenolic Coupling Reactions Using Hypervalent Iodine (III) Reagents and Their Application to the Synthesis of Amaryllidaceae Alkaloids" @default.
- W2019950616 cites W2949211683 @default.
- W2019950616 doi "https://doi.org/10.1002/chin.200106248" @default.
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