RIGID SPIRO ORTHO-AMINO AROMATIC KETONES - PREPARATION OF HIGHLY FLUORESCENT CARBONYL DERIVATIVES

Citation
Ca. Mateo et al., RIGID SPIRO ORTHO-AMINO AROMATIC KETONES - PREPARATION OF HIGHLY FLUORESCENT CARBONYL DERIVATIVES, New journal of chemistry, 20(3), 1996, pp. 371-374
Citations number
22
Categorie Soggetti
Chemistry
Journal title
ISSN journal
11440546
Volume
20
Issue
3
Year of publication
1996
Pages
371 - 374
Database
ISI
SICI code
1144-0546(1996)20:3<371:RSOAK->2.0.ZU;2-A
Abstract
A possible synthetic pathway to highly fluorescent spiro carbonyl deri vatives at room temperature is reported. N-Benzyl spiro[cyclopentane-1 ,2'-indolin-3'-one] can be considered as the first highly fluorescent phenone derivative at room temperature. The fluorescence is due to its rigid structure and the pi, pi nature of the first excited singlet s tate.