Concise Total Synthesis of Permethylated Anigopreissin A, a New Benzofuryl Resveratrol Dimer | Zendy

Chiummiento Lucia | Zendy; Funicello Maria | Zendy; Lopardo Maria Teresa | Zendy; Lupattelli Paolo | Zendy; Choppin Sabine | Zendy; Colobert Françoise | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Concise Total Synthesis of Permethylated Anigopreissin A, a New Benzofuryl Resveratrol Dimer

Author(s) -

Chiummiento Lucia,

Funicello Maria,

Lopardo Maria Teresa,

Lupattelli Paolo,

Choppin Sabine,

Colobert Françoise

Publication year - 2012

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.201101422

Subject(s) - chemistry , sonogashira coupling , moiety , wittig reaction , total synthesis , dimer , furan , stereochemistry , resveratrol , combinatorial chemistry , organic chemistry , palladium , catalysis , biochemistry

The versatile preparation of permethylated anigopreissin A ( 1 ) has been accomplished from methyl 3,5‐dihydroxybenzoate. The key steps of the synthesis are sequential Sonogashira and Suzuki cross‐couplings for the construction of the 2,3‐diarylbenzo[ b ]furan moiety and Wittig olefination for the introduction of the styryl group.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research