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- The base-catalysed rearrangement of α-acetolactate (2-hydroxy-2-methyl-3-oxobutanoate) : a novel carboxylate ion migration in a tertiary ketol rearrangement. David H. G. Crout, Charles J. R. Hedgecock
, J. Chem. Soc., Perkin Trans. 1
, 1979
, 1982
- Elemental fluorine Part 13. Gas–liquid thin film microreactors for selective direct fluorination. Richard D. Chambers, Darren Holling, Robert C. H. Spink, Graham Sandford
, Lab Chip
, 2001
, 1
, 132
- Asymmetric catalytic construction of fully substituted carbon stereocenters using acyclic α-branched β-ketocarbonyls: the “Methyl Rule” widely exists. Deqian Sun, Shuang Yang, Xinqiang Fang
, Org. Chem. Front.
, 2020
, 7
, 3557
- Stereochemistry of the decarboxylation of α-acetolactate (2-hydroxy-2-methyl-3-oxobutanoate) by the acetolactate decarboxylase of Klebsiella aerogenes. David H. G. Crout, Jennifer Littlechild, Michael B. Mitchell, Stephen M. Morrey
, J. Chem. Soc., Perkin Trans. 1
, 1984
, 2271
- Biosynthesis of valine and isoleucine: synthesis and biological activity of (2S)-α-acetolactic acid (2-hydroxy-2-methyl-3-oxobutanoic acid), and (2R)- and (2S)-α-acetohydroxybutyric acid (2-ethyl-2-hydroxy-3-oxobutanoic acid). Frank B. Armstrong, Elizabeth L. Lipscomb, David H. G. Crout, Michael B. Mitchell, Shimoga R. Prakash
, J. Chem. Soc., Perkin Trans. 1
, 1983
, 1197
- Diastereoselective intramolecular aldol ring closures of threonine derivatives leading to densely functionalised pyroglutamates related to oxazolomycin. Elizabeth A. Heaviside, Mark G. Moloney, Amber L. Thompson
, RSC Adv.
, 2014
, 4
, 16233
- Necic acid synthons. Part 4. Regioselectivity in the reactions of chloro and lodo derivatives of selected 3-hydroxy-2-methylenealkanoate esters with ethyl 2-methyl-3-oxobutanoate. Farouk Ameer, Siegfried E. Drewes, Mark S. Houston-McMillan, Perry T. Kaye
, J. Chem. Soc., Perkin Trans. 1
, 1985
, 1143
- Biosynthesis of austdiol and synthesis of a deuterium labelled biogenetic precursor. Lino Colombo, Cesare Gennari, Giovanni Poli, Carlo Scolastico, Fabrizio Aragozzini, Cosetta Merendi
, J. Chem. Soc., Perkin Trans. 1
, 1983
, 2745
- Biotransformations with acetolactate decarboxylase: unusual conversions of both substrate enantiomers into products of high optical purity. David H. G. Crout, Daniel L. Rathbone
, J. Chem. Soc., Chem. Commun.
, 1988
, 98
- Absolute configuration of the product of the acetolactate synthase reaction by a novel method of analysis using acetolactate decarboxylase. David H. G. Crout, Edward R. Lee, Daniel L. Rathbone
, J. Chem. Soc., Perkin Trans. 1
, 1990
, 1367