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Catalyst- and template-free condensation of photochromic difurylethene bisaldehyde with o-phenylenediamine led to selective formation of macrocyclic Schiff base [AB]2 product. Application of the same difurylethene bisaldehyde in the McMurry reaction… Click to show full abstract
Catalyst- and template-free condensation of photochromic difurylethene bisaldehyde with o-phenylenediamine led to selective formation of macrocyclic Schiff base [AB]2 product. Application of the same difurylethene bisaldehyde in the McMurry reaction resulted in cyclic dimer formation in moderate yield. No linear oligomers were observed in both approaches.
Keywords:
photochromic difurylethene;
difurylethene;
bisaldehyde potential;
building block;
potential building;
difurylethene bisaldehyde
Journal Title: Chemistry of Heterocyclic Compounds
Year Published: 2019
Link to full text (if available)
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Journal Title: Chemistry of Heterocyclic Compounds
Year Published: 2019
Link to full text (if available)
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recommendations!