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<Articles><Article><Journal><PublisherName></PublisherName><JournalTitle>DARU Journal of Pharmaceutical Sciences</JournalTitle><Volume>2</Volume><Issue>2-3</Issue></Journal><ArticleTitle>2D 1H -13C Heteronuclear Shift Correlation Of 2a - Hydroxy Aiantolactone From Pulicaria Undulata C.A. Mey</ArticleTitle><FirstPage>250</FirstPage><LastPage>259</LastPage><AuthorList><Author><FirstName></FirstName><LastName>A. Rustaiyan</LastName></Author><Author><FirstName></FirstName><LastName>Z. Habibi</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2015</Year><Month>10</Month><Day>06</Day></PubDate></History><Abstract>We have reported recently the isolation and characterization of several sesquiterpene lactones from Pulicaria undulata (1).The lactones were isolated from an Et20 - Petrol (1:3) fraction by different chromatographic techniques including HPLC (RP 8, MeOH - H2O, 13:7).In this way three eudesmanolides 1 - 3, a guaianolide 4, a nor -guaianolide 5, as well as the pseudoguaianolide 6 and the xanthanolide 7 were isolated. One of the eudesmanolides (2a - hydroxy aiantolactone), 1, was present as the main component.Such lactones being known as biologically active substances, we have decided to describe for the first time a detailed interpretation of proton, 1H -NMR, 13C - NMR and 2D lH -13C - heteronuclear shift correlation spectra of 2a - hydroxy aiantolactone. The stereochemistry of C - 2 , C - 7 and C - 8 was determined by the NOESY experiments, H - 7 and H - 8 are in the a configuration and H - 2 is in the b configuration.</Abstract><web_url>https://daru.tums.ac.ir/index.php/daru/article/view/30</web_url><pdf_url>https://daru.tums.ac.ir/index.php/daru/article/download/30/30</pdf_url></Article></Articles>
