10.6084/m9.figshare.5612995.v1 Ravindar Kotla Ravindar Kotla P. Aparna P. Aparna Shobha Donthabakthuni Shobha Donthabakthuni Radhakrishnamraju Ruddarraju Radhakrishnamraju Ruddarraju Adharvana Chari Murugulla Adharvana Chari Murugulla Gattu Sridhar Gattu Sridhar Enantioselective total synthesis of β-zearalenol from (<i>s</i>)- propylene oxide Taylor & Francis Group 2017 β-zearalenol Grignard reaction Grubbs RCM S-propylene oxide Yamaguchi macrolactonization 2017-11-17 15:10:25 Journal contribution https://tandf.figshare.com/articles/journal_contribution/Enantioselective_total_synthesis_of_-zearalenol_from_i_s_i_-_propylene_oxide/5612995 <p>The total synthesis of 14-membered resorcylic acid macrolide, β-Zearalenol was accomplished starting from commercially available enantiomerically pure propylene oxide and methyl 2,4-dihydroxy-6-methylbenzoate using Grignard reaction, Asymmetric dihydroxylation, Yamaguchi macrolactonization and RCM as key steps.</p>