Issue 23, 1990

Chemoenzymatic, enantiocomplementary, total asymmetric synthesis of leukotrienes-B3 and -B4

Abstract

The ketone 3 has been resolved using various enzyme-catalysed reactions and the enantiomer (+)-3 was transformed into the benzoate 8 while (–)-3 was converted into the esters 10 and 11; compounds 8 and 10 are complementary sections of leukotriene B4 while compounds 8 and 11 are late-stage synthons for leukotriene B3.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1990, 1661-1663

Chemoenzymatic, enantiocomplementary, total asymmetric synthesis of leukotrienes-B3 and -B4

I. C. Cotterill, G. Dorman, K. Faber, R. Jaouhari, S. M. Roberts, F. Scheinmann, J. Spreitz, A. G. Sutherland, J. A. Winders and B. J. Wakefield, J. Chem. Soc., Chem. Commun., 1990, 1661 DOI: 10.1039/C39900001661

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