Issue 7, 1999

Synthetic study of marine lobane diterpenes. Enantioselective syntheses of lobatrienolide and lobatrientriol from (+)-nopinone

Abstract

The first enantioselective syntheses of highly oxygenated lobane diterpenes, (+)-lobatrienolide 4 and (+)-lobatrientriol 5, have been achieved, starting with (4R,5R)-1-acetoxy-4-isopropenyl-5-methyl-5-vinylcyclohex-1-ene 10b which itself has been prepared from (+)-nopinone 7 as a versatile building block toward the asymmetric synthesis of natural products.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1999, 783-788

Synthetic study of marine lobane diterpenes. Enantioselective syntheses of lobatrienolide and lobatrientriol from (+)-nopinone

M. Kato, H. Kosugi, T. Ichiyanagi and O. Yamabe, J. Chem. Soc., Perkin Trans. 1, 1999, 783 DOI: 10.1039/A809983I

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