Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5262659 | Tetrahedron Letters | 2015 | 4 Pages |
Abstract
A facile and efficient protocol for the synthesis of pyrrole-fused benzoxazines has been developed via a novel molecular iodine-promoted denitration strategy, involving 2-aminophenols, acetylenic esters and β-nitrostyrene derivatives. This method offers the advantages of being nature friendly by avoiding use of metal catalyst and Brønsted acids, wide substrate scope, good yields, clean and simple methodology.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
A. Sagar, Venkata Nagarjuna Babu, Arnab Dey, Duddu S. Sharada,