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Title: Catalytic cascade hydroalkoxylation/isomerization/ [4 + 2] cycloaddition using enyne alcohols as latent dienes or dienophiles. Author: Guo R, Li KN, Gong LZ. Journal: Org Biomol Chem; 2013 Oct 21; 11(39):6707-12. PubMed ID: 24175323. Abstract: Enyne alcohols can react as precursors of either dienes or dienophiles with different substrates after hydroxylation and isomerization by gold catalysis. As such, oxa-bridged tricyclo[5.2.2.02,6]-undec-8-ene-3,5-dione derivatives have been obtained by the Diels–Alder reaction and tetrahydro-1H-furo[3,4-c]pyran derivatives could be accessed by the hetero-Diels–Alder cycloaddition.[Abstract] [Full Text] [Related] [New Search]