Thionyl chloride-pyridine mediated rearrangement. Synthesis of potential intermediates for (+) and (±)-occidol.

Article abstract of DOI:10.1080/00397919608004789

Thionyl chloride-pyridine mediated rearrangement of cylohexadienyl alcohols (2) and (8) has provided hyposantonin (3) and tetrahydronaphthalene (9), respectively, which in turn have served as potential intermediates for the synthesis of optically active a

Full text of DOI:10.1080/00397919608004789

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Synthetic Communications: An
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Thionyl Chloride-pyridine
Mediated Rearrangement.
Synthesis of Potential
Intermediates for (+) and (±)-
Occidol
a
a
Ajoy K. Banerjee & William Vera
a
Centre de Química , IVIC , Apartado 21827,
Caracas, 1020-A, Venezuela
Published online: 21 Aug 2006.
To cite this article: Ajoy K. Banerjee & William Vera (1996) Thionyl Chloride-pyridine
Mediated Rearrangement. Synthesis of Potential Intermediates for (+) and (±)-Occidol,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 26:24, 4641-4646, DOI: 10.1080/00397919608004789
To link to this article: http://dx.doi.org/10.1080/00397919608004789
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