Chiral δ-iodo-γ-lactones derived from cuminaldehyde, 2,5-dimethylbenzaldehyde and piperonal: chemoenzymatic synthesis and antiproliferative activity-Reference-Cited by-同舟云学术

Chiral δ-iodo-γ-lactones derived from cuminaldehyde, 2,5-dimethylbenzaldehyde and piperonal: chemoenzymatic synthesis and antiproliferative activity

Published:2016-04 Issue:6 Volume:27 Page:227-237
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Gładkowski Witold,Skrobiszewski Andrzej,Mazur Marcelina,Gliszczyńska Anna,Czarnecka Marta,Pawlak Aleksandra,Obmińska-Mrukowicz Bożena,Maciejewska Gabriela,Białońska Agata

Funder

Ministry of Science and Higher Education, Poland

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference53 articles.

1. 3-Phenyl-5-methyl-2H,5H-furan-2-ones: tuning antifungal activity by varying substituents on the phenyl ring

2. Synthesis and structure–antifungal activity Relationships of 3-Aryl-5-alkyl-2,5-dihydrofuran-2-ones and Their Carbanalogues: further refinement of tentative pharmacophore group

3. Synthesis and Antifungal Activity of Aromatic Bis-γ-lactones Analogous to Avenaciolide

4. New antifungal scaffold derived from a natural pharmacophore: Synthesis of α-methylene-γ-butyrolactone derivatives and their antifungal activity against Colletotrichum lagenarium

5. Antifungal 3,5-disubstituted furanones: From 5-acyloxymethyl to 5-alkylidene derivatives

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