Ir and pmr spectra of 2‐aryl‐4‐thiazolidinones. III. Stereochemical analysis of 2‐aryl‐3‐(2‐pyridyl)‐4‐thiazolidinones | Zendy

Vigorita M. G. | Zendy; Chimirri A. | Zendy; Grasso S. | Zendy; Fenech G. | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Ir and pmr spectra of 2‐aryl‐4‐thiazolidinones. III. Stereochemical analysis of 2‐aryl‐3‐(2‐pyridyl)‐4‐thiazolidinones

Author(s) -

Vigorita M. G.,

Chimirri A.,

Grasso S.,

Fenech G.

Publication year - 1979

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.5570160633

Subject(s) - chemistry , aryl , methylene , europium , stereochemistry , medicinal chemistry , organic chemistry , ion , alkyl

The long‐range coupling through the sulphur atom observed in a number of 2‐aryl‐3‐(2‐pyridyl)‐4‐thiazolidinones suggests that the C 2 proton and one of methylene protons are in a cis 1,3 diequatorial relationship. Some additional information concerning the preferred orientations of the substituents in this system are given from Eu(fod) 3 , [tris(1,1,1,2,2,3,3‐heptafluoro‐7,7‐dimethyloctane‐4,6‐dionato)]europium, induced shift data.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research