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- Enantioselective synthesis of the lactone moiety of the mevinic acids using D-xylose as a chiral precursor. Roberto Ballini, Enrico Marcantoni, Marino Petrini
, J. Chem. Soc., Perkin Trans. 1
, 1991
, 490
- Methyl (3R)-3-hydroxyhex-5-enoate as a precursor to chiral mevinic acid analogues. Frank Bennett, David W. Knight, Garry Fenton
, J. Chem. Soc., Perkin Trans. 1
, 1991
, 133
- An alternative approach to mevinic acid analogues from methyl (3R)-(–)-3-hydroxyhex-5-enoate and an extension to unambiguous syntheses of (6R)-(+)-and (6S)-(–)-goniothalamin. Frank Bennett, David W. Knight, Garry Fenton
, J. Chem. Soc., Perkin Trans. 1
, 1991
, 519
- The synthesis of the δ-lactone portion of the mevinic acids; a new non-acidic method of cyclic lactone expansion. Alan H. Davidson, Chris D. Floyd, Christopher N. Lewis, Peter L. Myers
, J. Chem. Soc., Chem. Commun.
, 1988
, 1417
- Oxidation of methyl p-tolyl sulfide with bakers' yeast: preparation of a synthon of the mevinic acid-type hypocholestemic agents. Jean Beecher, Ian Brackenridge, Stanley M. Roberts, Jenny Tang, Andrew J. Willetts
, J. Chem. Soc., Perkin Trans. 1
, 1995
, 1641
- Total syntheses of natural (+)-(4R,6R)-4-hydroxy-6-pentylvalerolactone and of (–)-(6R)-massoialactone. Frank Bennett, David W. Knight, Garry Fenton
, J. Chem. Soc., Perkin Trans. 1
, 1991
, 1543
- Chemical synthesis of 3-ethylcompactin, an inhibitor of 3-hydroxy-3-methylglutarylcoenzyme A reductase. Derrick L. J. Clive, K. S. Keshava Murthy, Rajan George, Mark J. Poznansky
, J. Chem. Soc., Perkin Trans. 1
, 1990
, 2099
- Biotransformation of organic sulfides. Herbert L. Holland
, Nat. Prod. Rep.
, 2001
, 18
, 171
- An entry to enantiomerically pure cis decalinic structures from carbohydrates. Claude Taillefumier, Yves Chapleur, Daniel Bayeul, André Aubry
, J. Chem. Soc., Chem. Commun.
, 1995
, 937
- HMG-CoA reductase inhibitors. A. Endo, K. Hasumi
, Nat. Prod. Rep.
, 1993
, 10
, 541