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

Research output: Contribution to journal › Article › peer-review

45 Scopus citations

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.

Original language	English
Pages (from-to)	1741-1743
Number of pages	3
Journal	Organic Letters
Volume	11
Issue number	8
DOIs	https://doi.org/10.1021/ol900196w
State	Published - 16 Apr 2009
Externally published	Yes

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

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.",

author = "Hu, {Xu Hong} and Feng Liu and Loh, {Teck Peng}",

year = "2009",

month = apr,

day = "16",

doi = "10.1021/ol900196w",

language = "英语",

volume = "11",

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journal = "Organic Letters",

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publisher = "American Chemical Society",

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T1 - Stereoelectronic versus steric tuning in the prins cyclization reaction

T2 - Synthesis of 2fi-trans pyranyl motifs

AU - Hu, Xu Hong

AU - Liu, Feng

AU - Loh, Teck Peng

PY - 2009/4/16

Y1 - 2009/4/16

N2 - 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.

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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U2 - 10.1021/ol900196w

DO - 10.1021/ol900196w

M3 - 文章

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AN - SCOPUS:65249114328

SN - 1523-7060

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SP - 1741

EP - 1743

JO - Organic Letters

JF - Organic Letters

IS - 8

ER -

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

Abstract

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