Quick, efficient conversion of phenones to conjugated trienes via germylene cycloaddition

Ryan D. Sweeder; Fern A. Edwards; Karla A. Miller; Mark M. Banaszak Holl; Jeff W. Kampf

doi:10.1021/om0108696

Quick, efficient conversion of phenones to conjugated trienes via germylene cycloaddition

Ryan D. Sweeder, Fern A. Edwards, Karla A. Miller, Mark M. Banaszak Holl, Jeff W. Kampf

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

17 Citations (Scopus)

Abstract

The conversion of phenones into conjugated trienes via germylene based cycloaddition reaction was investigated. The molecular modeling calculations based on DFT theory were performed to explore the comparative energetics of the formed products. The cycloaddition reaction at room temperature gave quantitative results that had some functional group tolerance.

Original language	English
Pages (from-to)	457-459
Number of pages	3
Journal	Organometallics
Volume	21
Issue number	3
DOIs	https://doi.org/10.1021/om0108696
Publication status	Published - 4 Feb 2002
Externally published	Yes

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title = "Quick, efficient conversion of phenones to conjugated trienes via germylene cycloaddition",

abstract = "The conversion of phenones into conjugated trienes via germylene based cycloaddition reaction was investigated. The molecular modeling calculations based on DFT theory were performed to explore the comparative energetics of the formed products. The cycloaddition reaction at room temperature gave quantitative results that had some functional group tolerance.",

author = "Sweeder, {Ryan D.} and Edwards, {Fern A.} and Miller, {Karla A.} and {Banaszak Holl}, {Mark M.} and Kampf, {Jeff W.}",

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T1 - Quick, efficient conversion of phenones to conjugated trienes via germylene cycloaddition

AU - Sweeder, Ryan D.

AU - Edwards, Fern A.

AU - Miller, Karla A.

AU - Banaszak Holl, Mark M.

AU - Kampf, Jeff W.

PY - 2002/2/4

Y1 - 2002/2/4

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AB - The conversion of phenones into conjugated trienes via germylene based cycloaddition reaction was investigated. The molecular modeling calculations based on DFT theory were performed to explore the comparative energetics of the formed products. The cycloaddition reaction at room temperature gave quantitative results that had some functional group tolerance.

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JO - Organometallics

JF - Organometallics

IS - 3

ER -

Quick, efficient conversion of phenones to conjugated trienes via germylene cycloaddition

Abstract

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