Two δ‐iodo‐γ‐lactones and two γ‐iodo‐δ‐lactones substituted at the β‐position with phenyl
or 4‐methylphenyl ring have been synthesized in both enantiomeric forms. The starting …

The Suzuki–Miyaura coupling reactions of 3-bromo-2 (5H)-furanones with a variety of
arylboronic acids, promoted by microwave heating, efficiently generate 3-aryl-2 (5H) …

In continuing the studies on the synthesis and evaluation of antifungal activity of the
analogues of (-) incrustoporine, the replacement of the phenyl moiety at C3 of the furanone …

5-氟代苯基糠酰胺的1,3,4-噻二唑衍生物的合成与除草活性测定Synthesis and Herbicidal
Activities of 1,3,4-T Page 1 2008 年第28 卷 有机化学 Vol. 28, 2008 第8 期, 1475~1478 …

The mechanism of action of the antifungal agent 3-(4-bromophenyl)-5-acyloxymethyl-2, 5-
dihydrofuran-2-one against Candida albicans was investigated by flow cytometry, using …

Thieme E-Journals - Synlett / Full Text DE EN Home Products Journals Books Book Series
Service Library Service Help Contact Portal SYNLETT Full-text search Full-text search Author …

Synthesis of analogues of antifungal podolactones via Pd-catalyzed processes revealed that
tandem 6-exo-alkyne carbopalladation/carbonylative lactonization sequence is strongly …

Abstract Several 1, 2‐diazaspiro [4, 4] nona‐2, 8‐diene‐6‐one derivatives were synthesised
via cycloaddition of nitrilimides to 3‐aryliden‐2 (3H)‐furanone derivatives. The formed …

The pharmacological effects of the presence of a sugar moiety, 1, 2, 3-triazole ring and silyl
groups in the structure of biologically active compounds have been extensively studied in …

The Suzuki cross-coupling reaction of arylboronic acids with a bromo-furanone has been
developed to prepare a series of substituted 2, 5-dihydrofuran-2-ones related to the fungal …