This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
ChemInform Abstract: 4, 6‐Diacetylresorcinol in Heterocyclic Synthesis. Part 1. Synthesis and Biological Evaluation of Some New Linearly and Angularly Substituted Pyrano[3, 2‐g]chromenes via Vilsmeier—Haack Formylation of 4, 6‐Diacetylresorcinol, Its Schiff Bases, and Hydrazones. Issue 9 (4th March 2014)
Record Type:
Journal Article
Title:
ChemInform Abstract: 4, 6‐Diacetylresorcinol in Heterocyclic Synthesis. Part 1. Synthesis and Biological Evaluation of Some New Linearly and Angularly Substituted Pyrano[3, 2‐g]chromenes via Vilsmeier—Haack Formylation of 4, 6‐Diacetylresorcinol, Its Schiff Bases, and Hydrazones. Issue 9 (4th March 2014)
Main Title:
ChemInform Abstract: 4, 6‐Diacetylresorcinol in Heterocyclic Synthesis. Part 1. Synthesis and Biological Evaluation of Some New Linearly and Angularly Substituted Pyrano[3, 2‐g]chromenes via Vilsmeier—Haack Formylation of 4, 6‐Diacetylresorcinol, Its Schiff Bases, and Hydrazones.
<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Most products are shown to have weak antimicrobial activities, and dicarboxaldehydes [(III) and (V)] exhibit moderate antibacterial activity against Gram‐positive bacteria, yeast, and fungus.</p> </abstract>