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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 34, 2004 - Issue 12
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Original Articles

A New Synthesis of 5,8‐Dimethyl‐2‐tetralone—A Potential Intermediate for the Synthesis of Ring‐A Aromatic Sesquiterpenes. Novel Transformation During Acetoxylation of 5,8‐Dimethyldihydronapthalene

Ajoy K. Banerjee Centro de Química, IVIC, Apartado 21827, Caracas, 1020‐A, VenezuelaCorrespondence[email protected]
,
William Vera Centro de Química, IVIC, Apartado 21827, Caracas, 1020‐A, Venezuela
&
Manuel S. Laya Centro de Química, IVIC, Apartado 21827, Caracas, 1020‐A, Venezuela
Pages 2301-2308 | Received 03 Mar 2004, Published online: 17 Aug 2006

Citations (4)

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Read on this site (1)

William J. Vera & Ajoy K. Banerjee. (2006) Formal Total Synthesis of (±)‐Occidol. Synthetic Communications 36:20, pages 3091-3094.
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Articles from other publishers (3)

Ajoy K. Banerjee, Willam J. Vera, Elvia V. Cabrera & Jennifer L. Sanchez. (2010) Transformation of 5,8-Dimethyl-1-Tetralone: Synthesis of Ar-Occidol. Journal of Chemical Research 34:5, pages 243-245.
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Vinod Kumar, Abhishek Sharma, Meenakshi Sharma, Upendra K. Sharma & Arun K. Sinha. (2007) DDQ catalyzed benzylic acetoxylation of arylalkanes: a case of exquisitely controlled oxidation under sonochemical activation. Tetrahedron 63:39, pages 9718-9723.
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Ajoy K. Banerjee, William Vera & Manuel S. Laya. (2004) A New Synthesis of 5,8‐Dimethyl‐2‐tetralone — A Potential Intermediate for the Synthesis of Ring‐A Aromatic Sesquiterpenes. Novel Transformation During Acetoxylation of 5,8‐Dimethyldihydronaphthalene.. ChemInform 35:44.
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