An unexpected four-component (3+1) reaction of an alkyl isocyanide with alkylidene-substituted Meldrum's acid in CH 2 Cl 2 at room temperature produces imino-furopyranones in good yields. The structures of the products are deduced from their IR, 1 H NMR, and 13 C NMR spectra and by X-ray analysis. T
Laccase-catalysed reaction between Meldrum's acid and catechols/hydroquinones – An investigation
✍ Scribed by Kidwai, Mazaahir; Jain, Arti; Sharma, Abha; Kuhad, Ramesh Chander
- Book ID
- 122590175
- Publisher
- Elsevier Science
- Year
- 2013
- Tongue
- English
- Weight
- 830 KB
- Volume
- 16
- Category
- Article
- ISSN
- 1631-0748
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v