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- Synthesis and mode of action of 1-substituted trans-cyclopropane 1,2-dicarboxylic acids: inhibitors of the methylaspartase reaction. Kamal Badiani, Philip Lightfoot, David Gani
, Chem. Commun.
, 1996
, 675
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Preparation of N-substituted aspartic acids via
enantiospecific conjugate addition of N-nucleophiles to fumaric acids
using methylaspartase: synthetic utility and mechanistic
implications 1. M. Saeed Gulzar, Mahmoud Akhtar, David Gani
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 649
- LX.—The conditions underlying the formation of unsaturated and cyclic compounds from halogenated open-chain derivatives. Part VI. Products derived from halogenated α-methylglutaric acids. Christopher Kelk Ingold
, J. Chem. Soc., Trans.
, 1925
, 127
, 387
- Carbon-13 labelling study of the coenzyme B12-dependent methylitaconate ⇌α-methyleneglutarate model rearrangement reaction and examination of potential cyclopropane intermediates. Paul Dowd, Roger Hershline
, J. Chem. Soc., Perkin Trans. 2
, 1988
, 61
- 114. Fused carbon rings. Part IX. The synthesis of stereoisomeric 1-methylcyclohexane-1 : 2-dicarboxylic acids and of various methylcyclohexanecarboxylicacetic acids. The influence of the angular methyl group on the stability of their anhydrides. R. P. Linstead, A. F. Millidge
, J. Chem. Soc.
, 1936
, 478
- Model experiments pertaining to the mechanism of action of vitamin B12-dependent α-methyleneglutarate mutase. Susan Ashwell, Alwyn G. Davies, Bernard T. Golding, Robyn Hay-Motherwell, Samson Mwesigye-Kibende
, J. Chem. Soc., Chem. Commun.
, 1989
, 1483