Sempervirenic acid,a diterpene acid from Solidago sempervirens

Sempervirenic acid, a new diterpene has been isolated from Solidago sempervirens and its structure determined by spectroscopic methods and chemical conversions to be 3β-acetoxy-labda-7,13-diene-15-oic acid.     

Isolation and structure of stephalic acid,a new clerodane diterpene from Stevia polycephala

From the methanolic extract of Stevia polycephala a new clerodane-type diterpene, stephalic acid, was isolated. The structure and stereochemistry were determined by a combination of spectral data and single-crystal X-ray analysis.     

3α-Angeloyloxy-2α-hydroxycativic acid,a new diterpene from Brickellia paniculata

The investigation of Brickellia paniculata resulted in the isolation of a new diterpene of the labdane type. It was identified as 3α-angeloyloxy-     

2α-iso-Valeroyloxyeperuic acid,a diterpene from Eupatorium petiolare

The diterpene acid 2α-iso-valeroyloxyeperuic acid was isolated from the aerial parts of Eupatorium petiolare. Its structure and stereochemist     

15-oxo-zoapatlin,a diterpene lactone from Viguiera maculata

The isolation of a new diterpene lactone and two known diterpenoid acids from the aerial parts of Viguiera maculata is reported.     

Tomexanthin,an oxepane diterpene from montanoa tomentosa

Chemical analysis of Montanoa tomentosa yielded an oxepane diterpene, tomexanthin, which was characterized by spectral comparison with the previously established zoapatanol.     

Poilaneic acid,a cembranoid diterpene from Croton poilanei

Poilaneic acid, a cembranoid diterpene from Croton poilanei, has been characterized as (1R*,2E,4Z,7E, 11Z)-12-carboxyl-1-isopropyl-4,8-dimethylcyclotetradecatetraene.     

A diterpene,a sesquiterpene quinone and flavanones from Wyethia helenioides

The aerial parts of Wyethia helenioides afforded a new geranyl nerol derivative (a 16-hydroxy-18-oic acid), two isomeric prenylated lavanones and a quinone derived from bisabolene. The structures were elucidated by spectroscopic methods and some chemical transformations. The chemotaxonomic situation is discussed briefly.     

Three diterpenes from Conyza podocephala

The investigation of Conyza podocephala afforded, in addition to known compounds, two clerodane derivatives and a dihydroxyfarnesyl methylfuran. Furthermore two new resorcinol derivatives were isolated. The structures were elucidated by spectroscopic methods and by chemical transformations. The chemotaxonomic situation within the genus is discussed briefly.     

A diterpene with a new carbon skeleton from Solidago altissima

An Indian sample of Solidago altissima afforded in addition to several clerodanes already isolated from other Solidago species, a diterpene with a new carbon skeleton. Furthermore a ketone and a new anethole derivative were present.     

A diterpene related to erythroxydiol from Helichrysum refluxum

From Helichrysum refluxum, in addition to known compounds, a diterpene acid related to erythroxydiol Z was isolated. The structure was elucidated by NMR techniques.     

Flavonoid dimers from the aerial parts of Conyza stricta

A new flavonoid dimer, strictatin (10), was identified from the aerial part of Conyza stricta, in addition to eleven known compounds. The structure of compound 10 was determined by spectral analyses, including 1D, 2D NMR and HR-ESI-MS experiments. All compounds were identified from Conyza stricta for the first time and flavonoid dimers were firstly reported from the family Asteraceae. The chemotaxonomic significance of the identified metabolites was discussed.     

Stereochemistry of strictic acid and related furano-diterpenes from conyza japonica and grangea maderaspatana

Extraction of Conyza japonica gave strictic acid, ent-2β-hydroxy-15,16-epoxy-3,13(16),14-clerodatrien-18-oic acid and 5,7-dihydroxy-3,8,4′-trimethoxyflavone. Extraction of Grangea maderaspatana gave (-)-hardwickiic acid, ent-15,16-epoxy-1,3,13(16),14-clerodatetraen-18-oic acid and 3-hydroxy-8-acetoxypentadeca-1,9,14-trien-4,6-diyne. The structure of ent-2β-hydroxy-15,16-epoxy-3,13(16),14-cleroclatrien-18-oic acid was deduced by spectroscopic methods and by partial synthesis from (-)-hardwickiic acid and the stereochemistries of strictic acid and (ent-15,16-epoxy-1,3,13(16),14-clerodatraen-18-oic acid were established by correlation with ent-2β-hydroxy-15,16-epoxy-3,13(16),14-clerodatrien-18-oic acid.     

Sphingolipids from Conyza canadensis

Sphingolipid 1 and its corresponding beta-D-glucopyranoside derivative 2 have been isolated from the ethylacetate fraction of Conyza canadensis along with beta-sitosterol 3, stigmasterol 4, beta-sitosterol 3-O-beta-D-glucoside 5 and harmine 6, reported for the first time from this species. The structures of 1 and 2 were elucidated through spectroscopy including two-dimensional NMR.