A concise route towards isoflavans | Zendy

Basuli Suchand | Zendy; Chinnabattigalla Sreenivasulu | Zendy; Gupta Kshitija | Zendy; Gedu Satyanarayana | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

A concise route towards isoflavans

Author(s) -

Basuli Suchand,

Chinnabattigalla Sreenivasulu,

Gupta Kshitija,

Gedu Satyanarayana

Publication year - 2021

Publication title -

journal of heterocyclic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.321

H-Index - 59

eISSN - 1943-5193

pISSN - 0022-152X

DOI - 10.1002/jhet.4158

Subject(s) - chemistry , intramolecular force , intermolecular force , combinatorial chemistry , catalysis , key (lock) , nanotechnology , stereochemistry , organic chemistry , molecule , computer science , materials science , computer security

Isoflavans have gained considerable interest owing to their potential health benefits. Herein, we have presented a straightforward strategy for isoflavans synthesis. The strategy features an intermolecular [Cu]‐catalyzed arylation of malonates and an intramolecular [Pd]‐catalyzed Buchwald coupling of hydroxy tethered bromoarenes as the key transformations. This protocol enabled the synthesis of a variety of isoflavan analogs.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research