A stereoselective synthesis of fully substituted tetrahydrofurans through 1,3-dipolar cycloaddition with cinnamaldehydes: An easy access to chroman derivatives

Lin Qiu; Xin Guo; Jun Zhou; Shunying Liu; Liping Yang; Xiang Wu; Wenhao Hu

doi:10.1039/c3ra44123g

A stereoselective synthesis of fully substituted tetrahydrofurans through 1,3-dipolar cycloaddition with cinnamaldehydes: An easy access to chroman derivatives

Lin Qiu
, Xin Guo
, Jun Zhou
, Shunying Liu^*
, Liping Yang
, Xiang Wu
, Wenhao Hu

^*此作品的通讯作者

化学与分子工程学院

East China Normal University

科研成果: 期刊稿件 › 文章 › 同行评审

11 引用（Scopus）

摘要

An efficient method of synthesizing the fully-substituted tetrahydrofuran through intermolecular dipolar cycloaddition reactions of aryl diazoesters, β-nitrostyrenes and cinnamaldehydes was developed. A novel cascade 1,3-dipolar cycloaddition/Michael addition reaction provides a rapid and step-economic construction of highly substituted polycyclic chroman frameworks.

源语言	英语
页（从-至）	20065-20070
页数	6
期刊	RSC Advances
卷	3
期	43
DOI	https://doi.org/10.1039/c3ra44123g
出版状态	已出版 - 21 11月 2013

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10.1039/c3ra44123g

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abstract = "An efficient method of synthesizing the fully-substituted tetrahydrofuran through intermolecular dipolar cycloaddition reactions of aryl diazoesters, β-nitrostyrenes and cinnamaldehydes was developed. A novel cascade 1,3-dipolar cycloaddition/Michael addition reaction provides a rapid and step-economic construction of highly substituted polycyclic chroman frameworks.",

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T1 - A stereoselective synthesis of fully substituted tetrahydrofurans through 1,3-dipolar cycloaddition with cinnamaldehydes

T2 - An easy access to chroman derivatives

AU - Qiu, Lin

AU - Guo, Xin

AU - Zhou, Jun

AU - Liu, Shunying

AU - Yang, Liping

AU - Wu, Xiang

AU - Hu, Wenhao

PY - 2013/11/21

Y1 - 2013/11/21

N2 - An efficient method of synthesizing the fully-substituted tetrahydrofuran through intermolecular dipolar cycloaddition reactions of aryl diazoesters, β-nitrostyrenes and cinnamaldehydes was developed. A novel cascade 1,3-dipolar cycloaddition/Michael addition reaction provides a rapid and step-economic construction of highly substituted polycyclic chroman frameworks.

AB - An efficient method of synthesizing the fully-substituted tetrahydrofuran through intermolecular dipolar cycloaddition reactions of aryl diazoesters, β-nitrostyrenes and cinnamaldehydes was developed. A novel cascade 1,3-dipolar cycloaddition/Michael addition reaction provides a rapid and step-economic construction of highly substituted polycyclic chroman frameworks.

UR - https://www.scopus.com/pages/publications/84886894395

U2 - 10.1039/c3ra44123g

DO - 10.1039/c3ra44123g

M3 - 文章

AN - SCOPUS:84886894395

SN - 2046-2069

VL - 3

SP - 20065

EP - 20070

JO - RSC Advances

JF - RSC Advances

IS - 43

ER -

A stereoselective synthesis of fully substituted tetrahydrofurans through 1,3-dipolar cycloaddition with cinnamaldehydes: An easy access to chroman derivatives

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