Results 91 to 100 of about 1,562 (203)
A novel spiro[indoline-3,2′-thiazolidine]-2,4′-dione derivative incorporating 3-chloro-4-fluorophenyl and 6-methoxypyridin-3-yl fragments was synthesized and characterized.
Dominika Kuceł +3 more
doaj +1 more source
Nonnatural amino acids are pivotal for expanding the functional diversity of peptides and proteins, enabling novel therapeutic opportunities. Mono-Boc-protected spirocyclization precursors have been developed as versatile intermediates for the ...
Puthiyaparambath, Sharathna +9 more
core +1 more source
Latest developments of spirooxindoles and their derivatives in medicinal chemistry
Spirooxindoles represent a pivotal class of heterocyclic compounds known for their diverse and potent biological activities. Naturally occurring spirooxindoles have been isolated from medicinal plants such as Flueggea virosa and Mitragyna speciosa, inspiring extensive research into their synthetic analogs.
Firoj, Hassan +4 more
openaire +2 more sources
A NHC-catalysed spiroannulation of isatin-derived enals and 1,3-dicarbonyl compounds has been developed, enabling enantioselective synthesis of synthetically important spirooxindole δ-lactones.
Xi-Na Cheng +5 more
core +1 more source
The efficient assembly of hydroindane derivatives incorporating a spirooxindole motif was realized via a new three-component domino reaction of (E)-4-(1-methyl-2-oxoindolin-3-ylidene)-3-oxobutanoates and two molecules of α,β-unsaturated aldehydes under ...
Kun Jiang (166885) +4 more
core +1 more source
This study discusses the synthesis and use of a new library of spirooxindole-benzimidazole compounds as inhibitors of the signal transducer and activator of p53, a protein involved in regulating cell growth and cancer prevention.
Assem Barakat +8 more
doaj +1 more source
Titanium(IV)-Catalyzed Stereoselective Synthesis of Spirooxindole-1-pyrrolines
A stereoselective cyclization between alkylidene oxindoles and 5-methoxyoxazoles has been developed using catalytic titanium(IV) chloride (as low as 5 mol %) to afford spiro[3,3′-oxindole-1-pyrrolines] in excellent yield (up to 99%) and ...
Joseph J. Badillo (1347651) +3 more
core +1 more source
Collective chemical syntheses of spirooxindole alkaloids
Spirooxindole alkaloids and their derivatives exhibit excellent biological activities in different aspects bearing a potential of pharmaceutical application. Many synthetic chemists were attracted to synthesize this type of compounds efficiently.
Cheung, Yuen Tsz
core
Screening of spirooxindole derivatives for anti-tumor activity on melanoma cells.
(A) Structure of analogues SOID-1 to SOID-12 inspired by natural product Sprotryprostatin B. (B) Effect of spirooxindole derivatives on melanoma cell growth.
Sangkil Nam (298303) +10 more
core +1 more source

