Synthesis and antimicrobial activity of [6′-methyl-4′-methoxy-2-oxo-2H-[1]-benzopyran)-2″,4″-dihydro-[1″, 2″, 4″]-triazol-3″-one and 3″-phenyl-thiazolidin-4″-one-phenoxymethyl derivatives of dipyranoquinoline
✍ Scribed by V. V. Mulwad; B. P. Langi; J. Chaskar; A. Chaskar
- Publisher
- Springer
- Year
- 2011
- Tongue
- English
- Weight
- 108 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0091-150X
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## Abstract 4‐Hydroxy‐2‐oxo‐2__H__‐1‐benzopyran‐3‐carboxaldehydes **2a‐d** are prepared from 4‐hydroxy‐2‐oxo‐2__H__‐1‐benzopyrans **1a‐d** __via__ the Vielsmeyer Haack reaction. The 4‐hydroxy‐2‐oxo‐3‐(3′oxo‐3′‐phenylprop‐1′‐enyl)‐2__H__‐1‐benzopyrans **3a‐d** are obtained from **2a‐d** __via__ the
## 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
The title compound, also known as intricatinol, C~17~H~14~O~5~, is a homoisoflavanoid that was isolated for the first time from the twigs and stems of __Caesalpinia digyna__ Rottler. The pyran ring is in an envelope form. O—H...O intramolecular hydrogen bonds are observed. Symmetry-related molecules