Organocatalytic Enantiospecific Total Synthesis of Butenolides.

Molecules

Catalysis Laboratory, School of Chemistry, University of Hyderabad, Central University (P.O.), Gachibowli, Hyderabad 500 046, India.

Published: July 2021

Biologically important, chiral natural products of butenolides, (-)-blastmycinolactol, (+)-blastmycinone, (-)-NFX-2, (+)-antimycinone, lipid metabolites, (+)-ancepsenolide, (+)-homoancepsenolide, mosquito larvicidal butenolide and their analogues were synthesized in very good yields in a sequential one-pot manner by using an organocatalytic reductive coupling and palladium-mediated reductive deoxygenation or organocatalytic reductive coupling and silica-mediated reductive deamination as the key steps.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8306825PMC
http://dx.doi.org/10.3390/molecules26144320DOI Listing

Publication Analysis

Top Keywords

organocatalytic reductive
8
reductive coupling
8
organocatalytic enantiospecific
4
enantiospecific total
4
total synthesis
4
synthesis butenolides
4
butenolides biologically
4
biologically chiral
4
chiral natural
4
natural products
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!