Structural Study of an Unusual Diels-Alder Adduct

Emilio Ghisalberti; Brian Skelton; Allan White

doi:10.1071/CH9922089

Structural Study of an Unusual Diels-Alder Adduct

Emilio Ghisalberti
, Brian Skelton
, Allan White

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

4 Citations (Scopus)

Abstract

The structure of the compound obtained on heating the naturally occurring clerodane furanoditerpene (1) had been formulated as (2) on the basis of spectroscopic studies. A single-crystal X-ray diffraction study on the dihydro derivative of (2) has confirmed this and provides support for the stereochemistry previously assigned to (1) on the basis of chemical evidence.

Original language	English
Pages (from-to)	2089-2091
Journal	Australian Journal of Chemistry: an international journal for chemical science
Volume	45
DOIs	https://doi.org/10.1071/CH9922089
Publication status	Published - 1992

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10.1071/CH9922089

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title = "Structural Study of an Unusual Diels-Alder Adduct",

abstract = "The structure of the compound obtained on heating the naturally occurring clerodane furanoditerpene (1) had been formulated as (2) on the basis of spectroscopic studies. A single-crystal X-ray diffraction study on the dihydro derivative of (2) has confirmed this and provides support for the stereochemistry previously assigned to (1) on the basis of chemical evidence.",

author = "Emilio Ghisalberti and Brian Skelton and Allan White",

year = "1992",

doi = "10.1071/CH9922089",

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AU - Ghisalberti, Emilio

AU - Skelton, Brian

AU - White, Allan

PY - 1992

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N2 - The structure of the compound obtained on heating the naturally occurring clerodane furanoditerpene (1) had been formulated as (2) on the basis of spectroscopic studies. A single-crystal X-ray diffraction study on the dihydro derivative of (2) has confirmed this and provides support for the stereochemistry previously assigned to (1) on the basis of chemical evidence.

AB - The structure of the compound obtained on heating the naturally occurring clerodane furanoditerpene (1) had been formulated as (2) on the basis of spectroscopic studies. A single-crystal X-ray diffraction study on the dihydro derivative of (2) has confirmed this and provides support for the stereochemistry previously assigned to (1) on the basis of chemical evidence.

U2 - 10.1071/CH9922089

DO - 10.1071/CH9922089

M3 - Article

SN - 0004-9425

VL - 45

SP - 2089

EP - 2091

JO - Australian Journal of Chemistry: an international journal for chemical science

JF - Australian Journal of Chemistry: an international journal for chemical science

ER -

Structural Study of an Unusual Diels-Alder Adduct

Abstract

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