Isomerisation of 2,2-dimethyl dimedone to (d,l) cis-chrysanthemic acid
β Scribed by Alain Krief; Guillaume Lorvelec; Stephane Jeanmart
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 117 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
D,L) cis-Chrysanthemic acid has been obtained in four steps from 2,2-dimethyl dimedone which involves Bamford-Stevens olefination and tandem cyclization-Grob fragmentation reactions.
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The effects of anoxic conditions on product inhibition and the stability of L-ATC hydrolase were investigated in the conversion of D,L-2-amino-A2-thiamline-4-carboxylic acid (D, L-ATC ) to L-cystine using the cell free extract enzyme of Pseudomonas sp. in the presence of hydroxylamine. At L-cysteine