Secondary Metabolites by Chemical Screening, 36 . Ulupyrinone and Ulufuranol: New Heteroaromatic Metabolites from  Streptomyces spina | Zendy

Henne Petra | Zendy; Grabley Susanne | Zendy; Thiericke Ralf | Zendy; Zeeck Axel | Zendy

Premium

Secondary Metabolites by Chemical Screening, 36 . Ulupyrinone and Ulufuranol: New Heteroaromatic Metabolites from Streptomyces spina

Author(s) -

Henne Petra,

Grabley Susanne,

Thiericke Ralf,

Zeeck Axel

Publication year - 1997

Publication title -

liebigs annalen

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 0947-3440

DOI - 10.1002/jlac.199719970523

Subject(s) - chemistry , streptomyces , chirality (physics) , stereochemistry , absolute configuration , strain (injury) , organic chemistry , genetics , bacteria , biology , chiral symmetry , physics , anatomy , quantum mechanics , nambu–jona lasinio model , quark

Chemical Screening with extracts of Actinomycetes strains resulted in the detection, isolation, and structural elucidation of two new heteroaromatic secondary metabolites, named ulupyrinone ( 1 ) and ulufuranol ( 2 ), from Streptomyces spina (strain FH‐S 2144). The absolute configuration of ulufuranol ( 2 ) was determined by analysis of the CD spectra of its dibenzoate, 3 , using the dibenzoate chirality rule.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research