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Synthesis of Biaryl Compounds by Vinylogous Michael Reactions

โœ Scribed by Jens Christoffers; Alexander Mann


Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
288 KB
Volume
2000
Category
Article
ISSN
1434-193X

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โœฆ Synopsis


Acceptor-substituted cycloalkenones 1 undergo an iron(III)catalyzed vinylogous Michael reactiona sequence of enone-dienol tautomerism, [4+2]-cycloaddition, and retro-aldol reactionwith quinone derivatives 3. A variety of products is obtained ranging from meta-terphenyl precursors 5 to


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