This submission belongs to the session b. Bioorganic, Medicinal and Natural Products of the event The 16th International Electronic Conference on Synthetic Organic Chemistry
Published date
26 Oct, 2012
Citation
ali Maleki, Mohammad Gorban Dekamin, Mohammad Eslami, Aqueous Synthesis of 2-Amino-tetrahydrobenzo[b]pyrans by a Green, Efficient and Simple Organocatalyst, in Proceedings of The 16th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2012, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-16-01115
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Aqueous Synthesis of 2-Amino-tetrahydrobenzo[b]pyrans by a Green, Efficient and Simple Organocatalyst
Mohammad Eslami 1
Mohammad Gorban Dekamin 1
ali Maleki 1
1. 1
Abstract
An efficient and convenient method has been developed for the synthesis of 2-amino-4H-tetrahydrobenzo[b]pyrans derivatives via one-pot , three-component condensation of malononitrile or ethyl cyanoacetete, dimedone and different aldehydes in the presence of a catalytic amount of potassium phthalimide-N-oxyl (POPINO), as a new organocatalyst, in aqueose media. A variety of 2-amino-tetrahydro[b]pyrans derivatives were obtained in high to excellent yield within short reaction times.
Keywords
Multicomponent reaction
dimedone
on water synthesis
2-amino-4H-tetrahydrobenzo[b]pyrans
potassium phthalimide-N-oxyl.
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