## Abstract For Abstract see ChemInform Abstract in Full Text.
A Novel Asymmetric ent-Kaurane Dimer from Isodon rubescens var. rubescens
โ Scribed by Quan-Bin Han; Zhen-Dan He; Chun-Feng Qiao; Hong-Xi Xu; Han-Dong Sun
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- German
- Weight
- 77 KB
- Volume
- 88
- Category
- Article
- ISSN
- 0018-019X
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โฆ Synopsis
Abstract
A novel asymmetric entโkaurane dimer, xindongnin P (1), was isolated from Isodon rubescens var. rubescens. Its structure was elucidated by detailed spectroscopic analysis. Compound 1 contains a tetrahydrofuran moiety whose formation leads to inversion of configuration at C(16). This differentiates 1 from known related dimers, which were isolated before from the Isodon genus. A likely biogenetic pathway from the alleged monomer precursor 3 is proposed.
๐ SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract Two new diterpenoids, rubescensin S (=(1__ฮฑ__,6__ฮฒ__,14__ฮฒ__)โ7__ฮฑ__,20โepoxyโ1,7,14โtrihydroxyโ16โoxoโ15,16โsecoโ__ent__โkauranโ6,15โolide; **1**) and rubescensin T (=(1__ฮฑ__,6__ฮฒ__,11__ฮฒ__,20__S__)โ7__ฮฑ__,20โepoxyโ1,6,7โtrihydroxyโ20โmethoxyโ8,15โsecoโ__ent__โkaurโ16โenโ11,15โolide; *