Combining Two-Directional Synthesis and Tandem Reactions:  Synthesis of Trioxadispiroketals

Paul McDermott; Robert A. Stockman

doi:10.1021/ol0479702

Combining Two-Directional Synthesis and Tandem Reactions: Synthesis of Trioxadispiroketals

Paul McDermott
, Robert A. Stockman

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

50 Citations (Scopus)

Abstract

A tandem bromonium ion-promoted cyclization of two pendant hydroxyl groups onto a central furan core provides a highly direct route to both the [5,5,5]- and the [6,5,6]-trioxadispiroketal ring systems.

Original language	English
Pages (from-to)	27-29
Number of pages	3
Journal	Organic Letters
Volume	7
Issue number	1
DOIs	https://doi.org/10.1021/ol0479702
Publication status	Published - 9 Dec 2005

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10.1021/ol0479702

Cite this

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title = "Combining Two-Directional Synthesis and Tandem Reactions: Synthesis of Trioxadispiroketals",

abstract = "A tandem bromonium ion-promoted cyclization of two pendant hydroxyl groups onto a central furan core provides a highly direct route to both the [5,5,5]- and the [6,5,6]-trioxadispiroketal ring systems.",

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AB - A tandem bromonium ion-promoted cyclization of two pendant hydroxyl groups onto a central furan core provides a highly direct route to both the [5,5,5]- and the [6,5,6]-trioxadispiroketal ring systems.

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