@article{Chimaladenne_Rama Krishna Surapureddi_Reddy Valluru_Kampli_Kumar Brahman_Babu Gudise_Vijaya Laxmi_2022, title={Synthesis of Multi-Substituted 4,5-Dihydrofurans: Microwave Assisted Reaction of β-Ketonitriles, Aldehydes and Pyridinium Phenacyl Salts via [1+1+3] Knoevenagel-Michael-Oxa-Michael Cyclization Triple Cascade Sequence}, volume={35}, url={https://asianpubs.org/index.php/ajchem/article/view/35_1_31}, DOI={10.14233/ajchem.2023.26932}, abstractNote={<p style="text-align: justify;">A microwave assisted protocol for the development of fully substituted dihydrofurans has been explained as a three component triple cascade reaction between pyridinium ylide, phenacyl nitriles and aldehydes. This [1+1+3] annulation protocol produced the dihydrofurans having two stereocentres. A total of 14 molecules have been synthesized with high chemical yields.</p>}, number={1}, journal={Asian Journal of Chemistry}, author={Chimaladenne, Venkateswarlu and Rama Krishna Surapureddi, Sri and Reddy Valluru, Krishna and Kampli, Anil and Kumar Brahman, Pradeep and Babu Gudise, Veera and Vijaya Laxmi, Somarapu}, year={2022}, month={Dec.}, pages={224–232} }