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Terpenoids-XXXIV: structure and stereochemistry of zingiberol and juniper camphor

Tipo de material: TextoTextoSeries ; Tetrahedron, 18(8), p.979-984, 1962Trabajos contenidos:
  • Varma, K.R
  • Jain, T.C
  • Bhaitacharyya, S.C
Recursos en línea: Resumen: Zingiberol has been shown to be a stereoisomeric mixture of peudesmol with rrans- and cis- ring juncture. This has been established by the comparative chemical and NMR studies of zingiberol, juniper camphor and Budesmol. Juniper camphor has been found to possess a cring juncture,
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Zingiberol has been shown to be a stereoisomeric mixture of peudesmol with rrans- and cis- ring juncture. This has been established by the comparative chemical and NMR studies of zingiberol, juniper camphor and Budesmol. Juniper camphor has been found to possess a cring juncture,

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