This review deals with the synthesis of unnatural and natural 2 (5H)-furanone derivatives
featuring bromine atoms on the heterocyclic ring and/or brominated substituents, which have …

A series of 3-aryl-5-acyloxymethyl-5, 6-dihydro-2H-pyran-2-ones, related to highly
antifungally active butenolides, was synthesized via cyclization of substituted δ-hydroxy …

Phenylacetic acids are efficiently synthesized from acetophenones via thiomorpholides
under Phase Transfer Catalytic (PTC) condition. The reaction proceeds efficiently by using …

Abstract A series of 81 3-phenyl-2 H-benzoxazine-2, 4 (3 H)-diones with substitution at C (6)
on the benzoxazine ring and on the phenyl moiety was synthesized; the compounds were …

Full article: Cycloisomerization of Olefinic Carboxylic Acids Catalyzed by Trifluoromethanesulfonic
Acid Skip to Main Content Taylor and Francis Online homepage Taylor and Francis Online …

5-Acetoxymethyl-3-(4-bromophenyl)-2, 5-dihydrofuran-2-one previously described as highly
antifungally active was found to provide the corresponding 5-methylene derivative via an …

Reduction of (Z)-β-butyltelluro-enones gives the corresponding γ-hydroxy vinylic tellurides
with retention of the double bond configuration. Reaction of γ-hydroxy vinylic tellurides with …

Six enantiomeric pairs of β-aryl-δ-iodo-γ-lactones 8a–c, 9a–c derived from cuminaldehyde,
2, 5-dimethylbenzaldehyde and piperonal were synthesized with high enantiomeric purities …

ABSTRACT Three 3-(halogenated phenyl)-5-acyloxymethyl-2, 5-dihydrofuran-2-ones were
evaluated for activity against 191 strains of common and emerging yeasts and Aspergillus …

An efficient synthesis of the antifungal agent (−)‐incrustoporin and analogues based on ring‐
closing metathesis (RCM) is described. The ready availability of various allyl alcohols …