α-N-Phthalimido-Oxy Isobutyrate-Mediated Deoxygenative Arylation: Total Synthesis of Alanenses A and B

13 January 2025, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Inspired by our biosynthetic hypothesis for alanense A, we developed two distinct methods for the deoxygenative arylation of α-N-phthalimido-oxy isobutyrate (NPIB), derived from hydroxyl groups adjacent to or conjugated with a carbonyl moiety. One approach utilizes photoredox catalysis to achieve a radical-mediated arylation reaction. Alternatively, we designed an acid-mediated arylation method that proceeds through a cationic intermediate. The acid-mediated approach was successfully applied to the total syntheses of alanenses A and B, as well as O7′-methyllacinilene E.

Keywords

NPIB
Total synthesis
Deoxygenative arylation
Natural products
Quaternary centers

Supplementary materials

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Description
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supporting information
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General procedures and characterization of newly synthesized compounds
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