Synthesis of anti-proliferative [3.3. 0] furofuranone derivatives by lactonization and functionalization of C-glycosyl compounds
J Ariztia, A Chateau, C Boura, C Didierjean… - Bioorganic & Medicinal …, 2021 - Elsevier
Abstract The [3.3. 0] furofuranone structure is found in numerous families of biologically
active natural products. We took advantage of the stereodiversity afforded by carbohydrate …
active natural products. We took advantage of the stereodiversity afforded by carbohydrate …
A concise synthesis of (+)-goniofufurone,(+)-7-epi-goniofufurone,(+)-crassalactones B and C
Y Zhang, X Liu, F Shui, F Zhou, J Cui, X Chen - Tetrahedron Letters, 2019 - Elsevier
The concise and efficient synthesis of (+)-goniofufurone,(+)-7-epi-goniofufurone,(+)-
crassalactones B and C were achieved in 6 to 7 steps from the known d-glucono-δ-lactone …
crassalactones B and C were achieved in 6 to 7 steps from the known d-glucono-δ-lactone …
Synthesis and antiproliferative activity of new thiazole hybrids with [3.3. 0] furofuranone or tetrahydrofuran scaffolds
New thiazole hybrids were synthesized and evaluated for their in vitro cytotoxicity against a
panel of human malignant cell lines. The key steps in the synthesis of hybrids 3–7 involved …
panel of human malignant cell lines. The key steps in the synthesis of hybrids 3–7 involved …
New Dephenylated Analogues of (–)-Goniofufurone: Optimization of Synthesis from l-Xylose
S Stanisavljević, M Popsavin, V Kojić, G Benedeković… - Synlett, 2024 - thieme-connect.com
Natural products containing highly oxygenated furanofuranone fragments are known for
their potent biological activity, but also for their challenging total synthesis. In this study, the …
their potent biological activity, but also for their challenging total synthesis. In this study, the …
Synthesis and structure of novel iodinated N-glycosyl-sulfonamides through Aza-Ferrier reaction of 2-substituted glycals
We obtained a series of novel N-(2-iodo-2, 3-dideoxy-2-en-glycopyranosides)-sulfonamides
via the Aza-Ferrier rearrangement of protected-2-iodoglycals in good yields and high …
via the Aza-Ferrier rearrangement of protected-2-iodoglycals in good yields and high …
[PDF][PDF] Dérivés C-glycosidiques pour l'imagerie bimodale TEP/FPIR Applications au marquage de dérivés peptidiques RGD
MN PELLEGRINI, MF SUZENET - 2021 - researchgate.net
Les dérivés saccharidiques sont souvent utilisés comme produits de départ chiraux pour
des synthèses totales et peuvent être également considérés comme des plates-formes …
des synthèses totales et peuvent être également considérés comme des plates-formes …