Journal ArticleOPEN ACCESS

1,8-Diazafloren-9-one with alkyl and aryl isocyanides in the presence of acetylenic esters: A facile synthesis of γ-spiroiminolactones

Journal of Heterocyclic Chemistry (2006) 43(2) 481-484
DOI: 10.1002/jhet.5570430234
22Citations
Citations of this article
9Readers
Mendeley users who have this article in their library.
Get full text

Abstract

The 1:1 intermediate generated by the addition of alkyl and aryl isocyanides to dialkyl acetylenedicarboxylate is trapped by 1,8-diazafloren-9- one to yield iminolactones in good yields.

Cite

CITATION STYLE

APA

Maghsoodlou, M. T., Hazeri, N., Khorassani, S. M. H., Marandi, G., & Nassiri, M. (2006). 1,8-Diazafloren-9-one with alkyl and aryl isocyanides in the presence of acetylenic esters: A facile synthesis of γ-spiroiminolactones. Journal of Heterocyclic Chemistry, 43(2), 481–484. https://doi.org/10.1002/jhet.5570430234

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free