Citation:

Patonay, T., R S. Varma*, A. Vass, A. Levai, AND J. Dudas. HIGHLY DIASTEREOSELECTIVE MICHAEL REACTION UNDER SOLVENT-FREE CONDITIONS USING MICROWAVES: CONJUGATE ADDITION OF FLAVANONE TO ITS CHALCONE PRECURSOR. TETRAHEDRON LETTERS. Elsevier Science Ltd, London, Uk, 42(8):1403-1406, (2001).

Description:

Microwave-assisted reaction of 2'-hydroxychalcones in the presence of DBU resulted in the formation of hitherto unknown dimers by conjugate addition of the intermediate cyclic ketone to the starting enone.

Record Details:

Record Type:DOCUMENT( JOURNAL/ PEER REVIEWED JOURNAL)

Product Published Date:02/12/2001

Record Last Revised:12/22/2005

Record ID: 64843

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Related Organizations:

Role :OWNER

Organization Name :US ENVIRONMENTAL PROTECTION AGENCY

Organization Name :OFFICE OF RESEARCH AND DEVELOPMENT

Organization Name :NATIONAL RISK MANAGEMENT RESEARCH LABORATORY

Organization Name :SUSTAINABLE TECHNOLOGY DIVISION

Document IDs:

EPA Number :EPA/600/J-01/052