Synthesis of the Natural Isomer of a Tetrahomoterpene Alcohol Obtained from the Codling Moth

Stephen B. Bowltis; John A. Katzenellenbogen

doi:10.1021/jo00955a042

Synthesis of the Natural Isomer of a Tetrahomoterpene Alcohol Obtained from the Codling Moth

Stephen B. Bowltis, John A. Katzenellenbogen

Chemistry

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

Abstract

The synthesis of the four possible stereoisomers of 7-methyl-3-propyl-2,6-decadien-l-ol, a tetrahomoterpene isolated from the codling moth, has been achieved, and spectroscopic and gas chromatographic comparison have established the natural material as the 2Z,6Z isomer.

Original language	English (US)
Pages (from-to)	2733-2734
Number of pages	2
Journal	Journal of Organic Chemistry
Volume	38
Issue number	15
DOIs	https://doi.org/10.1021/jo00955a042
State	Published - Jul 1 1973

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Organic Chemistry

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abstract = "The synthesis of the four possible stereoisomers of 7-methyl-3-propyl-2,6-decadien-l-ol, a tetrahomoterpene isolated from the codling moth, has been achieved, and spectroscopic and gas chromatographic comparison have established the natural material as the 2Z,6Z isomer.",

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AB - The synthesis of the four possible stereoisomers of 7-methyl-3-propyl-2,6-decadien-l-ol, a tetrahomoterpene isolated from the codling moth, has been achieved, and spectroscopic and gas chromatographic comparison have established the natural material as the 2Z,6Z isomer.

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Synthesis of the Natural Isomer of a Tetrahomoterpene Alcohol Obtained from the Codling Moth

Abstract

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