Publication | Closed Access
Chemoenzymatic, enantiocomplementary, total asymmetric synthesis of leukotrienes-B3 and -B4
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Citations
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References
1990
Year
Medicinal ChemistryKetone 3DerivativesTotal Asymmetric SynthesisBiochemistryNatural SciencesDiversity-oriented SynthesisBenzoate 8Organic ChemistryStereoselective SynthesisPharmacologyAsymmetric CatalysisEnantioselective SynthesisCompounds 8Natural Product Synthesis
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.
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