Stereoelectronic versus steric tuning in the prins cyclization reaction: Synthesis of 2fi-trans pyranyl motifs

Xu Hong Hu; Feng Liu; Teck Peng Loh

doi:10.1021/ol900196w

Stereoelectronic versus steric tuning in the prins cyclization reaction: Synthesis of 2fi-trans pyranyl motifs

Xu Hong Hu, Feng Liu, Teck Peng Loh

Nanyang Technological University

科研成果: 期刊稿件 › 文章 › 同行评审

45 引用（Scopus）

摘要

The use of carboalkoxyl allenic alcohol for the efficient synthesis of pyranyl motifs via Prlns cycllzatlon Is described. This method provides easy access to 2,6-trans dlhydropyrans In good yield and high dlastereoselectlvlty.

源语言	英语
页（从-至）	1741-1743
页数	3
期刊	Organic Letters
卷	11
期	8
DOI	https://doi.org/10.1021/ol900196w
出版状态	已出版 - 16 4月 2009
已对外发布	是

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abstract = "The use of carboalkoxyl allenic alcohol for the efficient synthesis of pyranyl motifs via Prlns cycllzatlon Is described. This method provides easy access to 2,6-trans dlhydropyrans In good yield and high dlastereoselectlvlty.",

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AB - The use of carboalkoxyl allenic alcohol for the efficient synthesis of pyranyl motifs via Prlns cycllzatlon Is described. This method provides easy access to 2,6-trans dlhydropyrans In good yield and high dlastereoselectlvlty.

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Stereoelectronic versus steric tuning in the prins cyclization reaction: Synthesis of 2fi-trans pyranyl motifs

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