Triethylammonium acetate-mediated domino-Knoevenagel-hetero-Diels–Alder reaction: synthesis of some angular polyheterocycles
摘要:
A solvent-cum catalyst, ionic liquid triethylammonium acetate-mediated one-pot procedure for the synthesis of some new angular benzopyrano[3,4-c]pyrano-fused pyrazoles, all of which incorporate a tertiary ring junction carbon, has been developed. The stereochemistry of the products has been confirmed by single-crystal X-ray diffraction data.
Gold-Catalyzed Synthesis of Polycyclic Enones from Carbon Tethered 1,3-Enynyl Carbonyls via Tandem Heteroenyne Metathesis and Nazarov Reaction
作者:Tienan Jin、Yoshinori Yamamoto
DOI:10.1021/ol801265s
日期:2008.7.17
An efficient and general Au(III)-catalyzed tandem reaction, heteroenyne metathesis and Nazarov cyclization, of 1,3-enynyl ketones to produce fused tri- and tetracyclic enones has been developed. The products were formed with excellent regioselectivity of the double bond position and with very high diastereoselectivities. In this reaction, the Au(III) catalyst exhibits dual roles for activating both alkynes and carbonyls.
Triethylammonium acetate-mediated domino-Knoevenagel-hetero-Diels–Alder reaction: synthesis of some angular polyheterocycles
作者:Narsidas J. Parmar、Bhavesh R. Pansuriya、Hitesh A. Barad、Bhagyashri D. Parmar、Rajni Kant、Vivek K. Gupta
DOI:10.1007/s00706-012-0873-7
日期:2013.6
A solvent-cum catalyst, ionic liquid triethylammonium acetate-mediated one-pot procedure for the synthesis of some new angular benzopyrano[3,4-c]pyrano-fused pyrazoles, all of which incorporate a tertiary ring junction carbon, has been developed. The stereochemistry of the products has been confirmed by single-crystal X-ray diffraction data.
3-Alkyl-1-benzoxepin-5-on-Derivate und 2-Alkyl-1, 4-naphthochinone aus 2-Acylaryl-propargyläthern