Synthesis of functionalized isoxazole-oxindole hybrids via on water, catalyst free vinylogous Henry and 1,6-Michael addition reactionsElectronic supplementary information (ESI) available. See DOI: 10.1039/c5ra14039k

Various 3-substituted-3-hydroxy isoxazole-oxindole hybrids were synthesized via the vinylogous Henry reaction of 3,5-dimethyl-4-nitroisoxazole and isatin using water as a reaction medium under catalyst free conditions at 50 °C. Systematic studies were carried out to understand the role of the water on the reaction by using D 2 O, brine, ethylene glycol and PEG-400 as a reaction medium along with organic solvents. Among all of these, water (0.170 mol concentration) was found be more efficient giving desired products in 82-99% yields in 45-120 min. Further the quaternary centre (3° alcohol) generated was used for the creation of a double bond which was again used for a 1,6-Michael reaction to produce highly functionalized isoxazole-oxindole derivatives. Various isoxazole-oxindole hybrids were synthesized via vinylogous Henry reaction of 3,5-dimethyl-4-nitroisoxazole and isatin under catalyst free conditions in water. The products obtained were functionalized using 1,6-Michael addition reaction.