Rearrangement of allyl aryl ethers; IV: Reaction of trimethylhydroquinone with cycloalkanediols

Synthesis

Volumn , Issue 6, 2000, Pages 809-812

  Novak, Lajos ^a   Kovács, Péter ^b   Kolonits, Pál ^a   Orovecz, Olivér ^a   Fekete, Jeno ^a   Szántay, Csaba ^a,b  

^a BUDAPEST UNIVERSITY OF TECHNOLOGY AND ECONOMICS   (Hungary)

^b CTRL RES INSTITUTE FOR CHEMISTRY   (Hungary)

Author keywords

Benzofurans; Cyclizations; Diols; Quinones; Rearrangements; Ring contraction; Spiro compounds

Indexed keywords

ALLYL COMPOUND; ETHER DERIVATIVE; HYDROQUINONE DERIVATIVE;

ARTICLE; CATALYSIS; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 0037682948     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2000-6278     Document Type: Article

References (10)

1. Part III: Novák, L.; Kovács, P.; Pirok, Gy.; Kolonits, P.; Hanania, M.; Donáth, K.; Szántay, Cs. Tetrahedron 1997, 53, 9789.
2. Novák, L.; Kovács, P.; Kolonits, P.; Hanania, M.; Fekete, J.; Szabó, É.; Szántay, Cs. Synthesis 1997, 909.
3. Novák, L.; Pirok, Gy.; Kovács, P.; Kolonits, P.; Szántay, Cs. Tetrahedron 1995, 51, 9367.
4. Novák, L.; Kovács, P.; Kolonits, P.; Szántay, Cs. Heterocycles 1994, 38, 177.
5. The reaction between phenol and cyclopentadiene has been described. The phosphonic acid catalyzed process afforded a mixture of p-cyclopent-2-en-l-yl phenol and the corresponding o-isomer; Dader, R.A. J. Am. Chem. Soc. 1953, 75, 5967. Dai, S.H.; Lin, C.Y.; Rao, D.V.; Stuber, F.A.; Carleton, P.S.; Ulrich, H. J. Org. Chem. 1985, 50, 1722.
6. The reaction between phenol and cyclopentadiene has been described. The phosphonic acid catalyzed process afforded a mixture of p-cyclopent-2-en-l-yl phenol and the corresponding o-isomer; Dader, R.A. J. Am. Chem. Soc. 1953, 75, 5967. Dai, S.H.; Lin, C.Y.; Rao, D.V.; Stuber, F.A.; Carleton, P.S.; Ulrich, H. J. Org. Chem. 1985, 50, 1722.
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