• TINA BISEN
• Prof. R. K. Garg

The synthetic sequence consists of the preparation of a properly functionalized epoxygeraniol derivative, and its subsequent stereoselective cyclization mediated by Ti(III). This last step implies a domino process that starts with a homolytic epoxide opening followed by a radical cyclization and regioselective elimination. This concerted process gives access to the cyclohexane moiety with stereochemical control of five of its six carbon atoms. In recent years, a number of studies for implementing assays for the isolation and characterization of trisporoids have been developed because they occur in fungi in very low concentrations and are chemically characterized for their relative instability.

cyclohexane , homolytic trisporoids; regioselective apocarotenoid, epoxygeraniol.

"A REVIEW STUDY FOR INTERMEDIATE COMPOUNDS DURING SYNTHESIS OF TRISPORIC ACIDS IN FUNGAL SPECIES", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.9, Issue 8, page no.c808-c818, August-2022, Available :http://www.jetir.org/papers/JETIR2208285.pdf

"A REVIEW STUDY FOR INTERMEDIATE COMPOUNDS DURING SYNTHESIS OF TRISPORIC ACIDS IN FUNGAL SPECIES", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.9, Issue 8, page no. ppc808-c818, August-2022, Available at : http://www.jetir.org/papers/JETIR2208285.pdf