- 著者
-
飯田 英夫
樹林 千尋
- 出版者
- The Society of Synthetic Organic Chemistry, Japan
- 雑誌
- 有機合成化学協会誌 (ISSN:00379980)
- 巻号頁・発行日
- vol.41, no.7, pp.652-666, 1983-07-01 (Released:2010-01-22)
- 参考文献数
- 116
- 被引用文献数
-
22
20
Nitrones are well-known to behave as 1, 3-dipoles and readily undergo thermal [3+2] cycloaddition reactions with olefins to produce isoxazolidine derivatives, which can be converted into β-amino alcohols by subsequent reductive N-O bond cleavage. The synthetically significant features of these reactions are carbon-carbon bond formation and introduction of nitrogen and oxygen functionality with concomitant high siteselectivities, regioselectivities, and stereoselectivities. Although this reaction mode has been alloted a more limited role in organic synthesis, more recent studies have demonstrated its general utility in the synthesis of a wide variety of natural products, particularly alkaloids. It is the purpose of this review to indicate the usefulness and synthetic aspects of nitrone methodology applicable to the natural products synthesis.