Recent advances in the synthesis of pamamycin-607

Article abstract of DOI:10.1080/10426509908546482

Using sultones as crucial intermediates, a short and highly stereoselective synthesis of a precursor of the larger fragment and the methyl ester of the smaller fragment of the macrodiolide pamamycin-607 was achieved.

Full text of DOI:10.1080/10426509908546482

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Phosphorus, Sulfur, and
Silicon and the Related
Elements
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Recent Advances
in the Synthesis of
Pamamycin-607
Peter Metz & Heiko Bernsmann
a Institut für Organische Chemie, TU
Dresden, Mommsenstr, 13, D-01062
Dresden, Germany
b Institut für Organische Chemie, TU
Dresden, Mommsenstr, 13, D-01062
Dresden, Germany
Published online: 17 Mar 2008.
To cite this article: Peter Metz & Heiko Bernsmann (1999): Recent Advances
in the Synthesis of Pamamycin-607, Phosphorus, Sulfur, and Silicon and the
Related Elements, 153:1, 383-384
To link to this article: http://dx.doi.org/10.1080/10426509908546482
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