Heteroannulation of naphthoquinones. Studies on the reaction of 2‐bromo‐2,3‐dihydronaphthoquinone derivatives with 1,2‐binucleophiles. | Zendy

Couladouros Elias A. | Zendy; Plyta Zoi F. | Zendy; Iliadis Theodoros | Zendy; Roussis Vassilios | Zendy; Papageorgiou Vassilios P. | Zendy

Premium

Heteroannulation of naphthoquinones. Studies on the reaction of 2‐bromo‐2,3‐dihydronaphthoquinone derivatives with 1,2‐binucleophiles.

Author(s) -

Couladouros Elias A.,

Plyta Zoi F.,

Iliadis Theodoros,

Roussis Vassilios,

Papageorgiou Vassilios P.

Publication year - 1996

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.5570330331

Subject(s) - chemistry , stereochemistry , combinatorial chemistry , organic chemistry , medicinal chemistry

Heterocyclic derivatives of naphthoquinones were synthesized via their 2‐bromo‐2,3‐dehydro‐intermediates. This new route may lead to the formation of benzo[ a ]phenothiazin‐5‐ones, benzo[ f ]quinoxalin‐6‐ones as well as their 1,4 (or 7,10) dihydroxy‐derivatives in high yields. The possible mechanisms involved in the formation of these compounds are discussed.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research