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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