Fe3O4@MCM@ZrCI2: A Practical Magnetic Mesoporous Zirconium-Based Nanocomposite as a Reusable Catalyst for the Synthesis of Spirooxindoles

In the present study, we aimed to investigate the catalytic role of the newly reported MCM-41 -based nanocomposite in which the low acidity of this mesoporous moiety was favourably improved via the stabilization of zirconium nanoparticles and was magnetized to make a facile work-up procedure as an applicable and efficient method. The prepared Fe3O4@MCM-41 @ZrCI2 nanocomposite was successfully characterized using different analyses and then it was favourably exploited for the synthesis of spirooxindoles as the most prominent spiro compounds. As predicted, Fe3O4@MCM- 41 @ZrCI2 showed considerable efficiency in the promotion of the studied reaction.

New Methods for the Synthesis of Spirocyclic Cephalosporin Analogues

Spiro compounds provide attractive targets in drug discovery due to their inherent three-dimensional structures, which enhance protein interactions, aid solubility and facilitate molecular modelling. However, synthetic methodology for the spiro-functionalisation of important classes of penicillin and cephalosporin β-lactam antibiotics is comparatively limited. We report a novel method for the generation of spiro-cephalosporin compounds through a Michael-type addition to the dihydrothiazine ring. Coupling of a range of catechols is achieved under mildly basic conditions (K2CO3, DMF), giving the stereoselective formation of spiro-cephalosporins (d.r. 14:1 to 8:1) in moderate to good yields (28−65%).

Highly diastereoselective entry to chiral oxindole-based β-amino boronic acids and spiro derivatives

We here describe the first Cu-catalysed, diastereoselective 1,2-addition of 1,1-diborylmethane to chiral ketimines for the synthesis of quaternary stereocenters and spiro compounds. The method provides easy access to a range...

Synthesis of optically active 2-amino-1′-benzyl-2′,5-dioxo-5H-spiro[indeno[1,2-b]pyran-4,3′-indoline]-3-carbonitriles catalyzed by a bifunctional squaramide derived from quinine

The first organocatalytic asymmetric reaction of propylene malononitrile with oxoindole and 1,3-indandione for the synthesis of chiral indeno-spiro compounds has been developed.