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Stereochemical course of the hydration reaction catalysed by β-hydroxydecanoylthioester dehydrase. John M. Schwab, John B. Klassen, Asif Habib , J. Chem. Soc., Chem. Commun. , 1986 , 357

Ester coupling reactions – an enduring challenge in the chemical synthesis of bioactive natural products. Michail Tsakos, Eva S. Schaffert, Lise L. Clement, Nikolaj L. Villadsen, Thomas B. Poulsen , Nat. Prod. Rep. , 2015 , 32 , 605

NMR conformational analysis of biosynthetic precursor-type lipid A: monomolecular state and supramolecular assembly. Masato Oikawa, Tetsuya Shintaku, Naohiro Fukuda, Harald Sekljic, Yoshiyuki Fukase, Hiroaki Yoshizaki, Koichi Fukase, Shoichi Kusumoto , Org. Biomol. Chem. , 2004 , 2 , 3557

The pentaketide hydroxyacyl intermediate in aspyrone biosynthesis in Aspergillus melieus is shown to be the (S)-enantiomer using deuterium-labelled precursors and ²H NMR. Alison M. Hill, James Staunton , J. Chem. Soc., Chem. Commun. , 1995 , 861

β-Hydroxydecanoylthioester dehydraes. Steric course at substrate C–4 in the enzyme–catalysed allylic rearrangement. John M. Schwab, John B. Klassen , J. Chem. Soc., Chem. Commun. , 1984 , 296

The biosynthesis of polyketides. T. J. Simpson , Nat. Prod. Rep. , 1985 , 2 , 321

Chapter 14. Biosynthesis. T. J. Simpson , Annu. Rep. Prog. Chem., Sect. B: Org. Chem. , 1986 , 83 , 347