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>