<b>Terpenses. I. The Absolute Configuration of (-)-Umbellulone and the Thujane Terpenes</b>

Smith, Howard E.; Gordon, A. W.

doi:10.1021/ja00873a049

J. Am. Chem. Soc.

1962

DOI: 10.1021/ja00873a049

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Terpenses. I. The Absolute Configuration of (-)-Umbellulone and the Thujane Terpenes

Howard E. Smith¹,

A. W. Gordon²

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1966

1971

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Die Ableitung der Stereochemie von 1‐Isopropyl‐4‐methyl‐bicyclo[3.1.0]hexan (cis‐und trans‐Thujan) durch Protonenresonanz‐Spektroskopie

Dieffenbacher¹,

Philipsborn²

1966

Helvetica Chimica Acta

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Isomeren. Thujan R ist 97,6% optisch reines Isomeres mit 2,4O/, Thujan A, wahrend letzteres noch 11% Thujan R enthalten soll. Die von chemischen Argumenten unabhangige Kestinimung der relativen Konfigurationen und eine Studie der Konformationen dieser beiden Kohlenwasserstoffe durch 100-MHz-ProtonenresonanzSpektroskopie ist Gegenstand der nachfolgenden Arbeit. Orientierende Messungen der Protonenspektren bei 60 MHz sind bereits in der vorgenannten Arbeit ausgewertet worden.

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Die Ableitung der Stereochemie von 1‐Isopropyl‐4‐methyl‐bicyclo[3.1.0]hexan (cis‐und trans‐Thujan) durch Protonenresonanz‐Spektroskopie

Dieffenbacher¹,

Philipsborn²

1966

Helvetica Chimica Acta

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show abstract

The absolute configuration of thujane

et al. 1966

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Essential oils and related products

Guenther¹,

Gilbertson²,

Koenig³

1971

Anal. Chem.

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Terpenses. I. The Absolute Configuration of (-)-Umbellulone and the Thujane Terpenes

Cited by 3 publications

References 0 publications

Die Ableitung der Stereochemie von 1‐Isopropyl‐4‐methyl‐bicyclo[3.1.0]hexan (cis‐und trans‐Thujan) durch Protonenresonanz‐Spektroskopie

Die Ableitung der Stereochemie von 1‐Isopropyl‐4‐methyl‐bicyclo[3.1.0]hexan (cis‐und trans‐Thujan) durch Protonenresonanz‐Spektroskopie

The absolute configuration of thujane

Essential oils and related products

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