Next Article in Journal
New Diterpenoid Alkaloids from the Roots of Delphinium tiantaishanense
Previous Article in Journal
Acylated Flavone Glycosides from the Roots of Saussurea lappa and Their Antifungal Activity
Molecules 2007, 12(3), 345-352; doi:10.3390/12030345
Article

Synthesis of New 1,3-Disubstituted-2,3-dihydro-1H-naphth[1,2e][1,3]oxazines

* ,  and
Received: 15 February 2007 / Revised: 2 March 2007 / Accepted: 3 March 2007 / Published: 7 March 2007
Download PDF [80 KB, uploaded 18 June 2014]

Abstract

1,3-Disubstituted-2,3-dihydro-1H-naphth[1,2-e][1,3]oxazines were prepared through the ring-closurereactions of the aminobenzylnaphthols with substituted aryl-andheteroarylaldehydes.
Keywords: Biological activity; ring-closure reactions; naphth-1; 3-oxazines; amino-benzylnaphthols Biological activity; ring-closure reactions; naphth-1; 3-oxazines; amino-benzylnaphthols
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Share & Cite This Article

Further Mendeley | CiteULike
Export to BibTeX |
EndNote
MDPI and ACS Style

Turgut, Z.; Pelit, E.; Köycü, A. Synthesis of New 1,3-Disubstituted-2,3-dihydro-1H-naphth[1,2e][1,3]oxazines. Molecules 2007, 12, 345-352.

View more citation formats

Related Articles

Article Metrics

Comments

Citing Articles

[Return to top]
Molecules EISSN 1420-3049 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert