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Barton-Zard reaction of nitrostilbenes with ethyl isocyanoacetate carried out in EtOH in the presence of K2CO3 allowed us to minimize the formation of side products and to obtain 3,4-diarylpyrrole-2-carboxylates in… Click to show full abstract
Barton-Zard reaction of nitrostilbenes with ethyl isocyanoacetate carried out in EtOH in the presence of K2CO3 allowed us to minimize the formation of side products and to obtain 3,4-diarylpyrrole-2-carboxylates in high yields.
Keywords:
fragments natural;
carboxylates key;
synthesis diarylpyrrole;
efficient synthesis;
key fragments;
diarylpyrrole carboxylates
Journal Title: Russian Chemical Bulletin
Year Published: 2018
Link to full text (if available)
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Journal Title: Russian Chemical Bulletin
Year Published: 2018
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!