Synthesis of 2,3-dihydro-4-pyranones from epoxides via intermolecular [4+2] cycloaddition reaction

Kiran Indukuri; Somasekhar Bondalapati; Sabera Sultana; Anil Kumar Saikia

doi:10.1039/c2ra21468g

Synthesis of 2,3-dihydro-4-pyranones from epoxides via intermolecular [4+2] cycloaddition reaction

Kiran Indukuri, Somasekhar Bondalapati, Sabera Sultana, Anil Kumar Saikia

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

8 Scopus citations

Abstract

An efficient synthesis of 2,3-dihydro-4-pyranones from epoxides and 3-alkoxycyclobutanones via an intermolecular [4+2] cycloaddition reaction, mediated by boron trifluoride etherate has been developed. The reaction is diastereoselective and gives trans diastereomers in excess.

Original language	English
Pages (from-to)	9398-9402
Number of pages	5
Journal	RSC Advances
Volume	2
Issue number	25
DOIs	https://doi.org/10.1039/c2ra21468g
State	Published - 21 Oct 2012
Externally published	Yes

ASJC Scopus subject areas

General Chemistry
General Chemical Engineering

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abstract = "An efficient synthesis of 2,3-dihydro-4-pyranones from epoxides and 3-alkoxycyclobutanones via an intermolecular [4+2] cycloaddition reaction, mediated by boron trifluoride etherate has been developed. The reaction is diastereoselective and gives trans diastereomers in excess.",

author = "Kiran Indukuri and Somasekhar Bondalapati and Sabera Sultana and Saikia, {Anil Kumar}",

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AU - Indukuri, Kiran

AU - Bondalapati, Somasekhar

AU - Sultana, Sabera

AU - Saikia, Anil Kumar

PY - 2012/10/21

Y1 - 2012/10/21

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AB - An efficient synthesis of 2,3-dihydro-4-pyranones from epoxides and 3-alkoxycyclobutanones via an intermolecular [4+2] cycloaddition reaction, mediated by boron trifluoride etherate has been developed. The reaction is diastereoselective and gives trans diastereomers in excess.

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Synthesis of 2,3-dihydro-4-pyranones from epoxides via intermolecular [4+2] cycloaddition reaction

Abstract

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