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- 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
- 1,2-Bond shift isomerization on copper. Mihály Bartók, Árpád Molnár
, J. Chem. Soc., Chem. Commun.
, 1980
, 1178
- Studies on pyruvate decarboxylase: acyloin formation from aliphatic, aromatic and heterocyclic aldehydes. David H. G. Crout, Howard Dalton, David W. Hutchinson, Masanori Miyagoshi
, J. Chem. Soc., Perkin Trans. 1
, 1991
, 1329
- Modelling the ambient distribution of organic compounds during the August 2003 ozone episode in the southern UK. Steven R. Utembe, Michael E. Jenkin, Richard G. Derwent, Alastair C. Lewis, James R. Hopkins, Jacqueline F. Hamilton
, Faraday Discuss.
, 2005
, 130
, 311
- Stereospecific formation of R-aromatic acyloins by Zymomonas mobilis pyruvate decarboxylase. Stephen Bornemann, David H. G. Crout, Howard Dalton, Vladimír Kren, Mario Lobell, Gregory Dean, Nicholas Thomson, Margaret M. Turner
, J. Chem. Soc., Perkin Trans. 1
, 1996
, 425
- Catalytic mechanism of acetolactate decarboxylase from Brevibacillus brevis towards both enantiomers of α-acetolactate. Chenxiao Zhao, Hao Su, Yongjun Liu
, RSC Adv.
, 2016
, 6
, 80621
- Skeletal rearrangement of α-hydroxy-ketones upon electron impact. M. J. Frearson, D. M. Brown
, J. Chem. Soc. C
, 1968
, 2909
- Sustainable energy and fuels from biomass: a review focusing on hydrothermal biomass processing. Koray Alper, Kubilay Tekin, Selhan Karagöz, Arthur J. Ragauskas
, Sustainable Energy Fuels
, 2020
, 4
, 4390
- Stereoelectronic control of the base-catalysed rearrangement of 2-hydroxy-3-oxocarboxylates. David H. G. Crout, Edward R. Lee, David P. J. Pearson
, J. Chem. Soc., Perkin Trans. 2
, 1991
, 381