1H and 13C NMR signal assignments of a novel Baeyer-Villiger originated diterpene lactone

Henriete S. Vieira; Jacqueline A. Takahashi; A. A.Leslie Gunatilaka; Maria Amélia D. Boaventura

doi:10.1002/mrc.1738

¹H and ¹³C NMR signal assignments of a novel Baeyer-Villiger originated diterpene lactone

Henriete S. Vieira, Jacqueline A. Takahashi, A. A.Leslie Gunatilaka, Maria Amélia D. Boaventura

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

4 Scopus citations

Abstract

A highly rearranged novel dilactone was the single product isolated from Baeyer-Villiger oxidation of a norketone prepared from grandiflorenic acid, a natural kaurane diterpene. The complete ¹H and ¹³C NMR assignment is presented for this novel compound that showed discrete in vitro antibacterial activity.

Original language	English (US)
Pages (from-to)	146-150
Number of pages	5
Journal	Magnetic Resonance in Chemistry
Volume	44
Issue number	2
DOIs	https://doi.org/10.1002/mrc.1738
State	Published - Feb 2006

Keywords

1D NMR
2D NMR
Baeyer-Villiger oxidation
Kaurane diterpene lactones

ASJC Scopus subject areas

General Chemistry
General Materials Science

Access to Document

10.1002/mrc.1738

Cite this

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abstract = "A highly rearranged novel dilactone was the single product isolated from Baeyer-Villiger oxidation of a norketone prepared from grandiflorenic acid, a natural kaurane diterpene. The complete 1H and 13C NMR assignment is presented for this novel compound that showed discrete in vitro antibacterial activity.",

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AU - Boaventura, Maria Amélia D.

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