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^*

^*Corresponding author for this work

Nanyang Technological University

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

45 Citations (Scopus)

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
Publication status	Published - Apr 16 2009
Externally published	Yes

ASJC Scopus Subject Areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol900196w

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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 = "English",

volume = "11",

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journal = "Organic Letters",

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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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AN - SCOPUS:65249114328

SN - 1523-7060

VL - 11

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JO - Organic Letters

JF - Organic Letters

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ER -

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

Abstract

ASJC Scopus Subject Areas

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