Molecular iodine-catalyzed combinatorial library synthesis of 2-amino-3-cyano-4H-pyran derivatives at ambient temperature
Publish place: Journal of Communications In Catalysis، Vol: 1، Issue: 2
Publish Year: 1397
Type: Journal paper
Language: English
View: 617
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Document National Code:
JR_CIC-1-2_002
Index date: 25 May 2019
Molecular iodine-catalyzed combinatorial library synthesis of 2-amino-3-cyano-4H-pyran derivatives at ambient temperature abstract
An efficient and simple synthesis of some 2-amino-3-cyano-4H-pyran derivatives was developed via the one-pot and three-component reaction of aldehydes, ethyl acetoacetate, and malononitrile in the presence of ammonium acetate at room temperature using catalytic amount of iodine. The key advantages of this method are the easy access to various substituted 2-amino-3-cyano-4H-pyran derivatives, short reaction times and high yields.
Molecular iodine-catalyzed combinatorial library synthesis of 2-amino-3-cyano-4H-pyran derivatives at ambient temperature Keywords:
Molecular iodine-catalyzed combinatorial library synthesis of 2-amino-3-cyano-4H-pyran derivatives at ambient temperature authors
Adeleh Moshtaghi Zonouz
Chem. Dep., Fac. Sci, Azarbaijan Shahid Madani Univ., Tabriz, Iran
Saeed Behjat
Naft research center