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A Novel Asymmetric ent-Kaurane Dimer from Isodon rubescens var. rubescens

โœ 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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โœฆ Synopsis


Abstract

A novel asymmetric entโ€kaurane 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.


๐Ÿ“œ SIMILAR VOLUMES


Ent-Kaurane Diterpenoids from Isodon rub
โœ Quan-Bin Han; Wei-Lie Xiao; Yun-Heng Shen; Han-Dong Sun ๐Ÿ“‚ Article ๐Ÿ“… 2004 ๐Ÿ› John Wiley and Sons โš– 14 KB ๐Ÿ‘ 1 views

## Abstract For Abstract see ChemInform Abstract in Full Text.

Rubescensins S and T: Seco-ent-Kaurane D
โœ Quan-Bin Han; Rong-Tao Li; Ji-Xia Zhang; Han-Dong Sun ๐Ÿ“‚ Article ๐Ÿ“… 2004 ๐Ÿ› John Wiley and Sons ๐ŸŒ German โš– 112 KB

## Abstract Two new diterpenoids, rubescensin S (=(1__ฮฑ__,6__ฮฒ__,14__ฮฒ__)โ€7__ฮฑ__,20โ€epoxyโ€1,7,14โ€trihydroxyโ€16โ€oxoโ€15,16โ€secoโ€__ent__โ€kauranโ€6,15โ€olide; **1**) and rubescensin T (=(1__ฮฑ__,6__ฮฒ__,11__ฮฒ__,20__S__)โ€7__ฮฑ__,20โ€epoxyโ€1,6,7โ€trihydroxyโ€20โ€methoxyโ€8,15โ€secoโ€__ent__โ€kaurโ€16โ€enโ€11,15โ€olide; *