Preparation of pure optically active (3s)- and (4s)- tert -butylcyclohexenes
β Scribed by S. K. Sadozai; J. A. Lepoivre; R. A. Dommisse; F. C. Alderweireldt
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2010
- Weight
- 312 KB
- Volume
- 89
- Category
- Article
- ISSN
- 0037-9646
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## I I94 The synthesis was performed on a 10 g scale and (S)-a-methylserine had an enantiomeric purity of >99% as assessed by gas chromatographic enantiomeric analysis.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
2S,3S)-3-methyl-and 3-isopropylaspartic acids were synthesized by bioconversion of the corresponding alkylfumarates (mesaconate and 3-isopropylfumarate) using pmethylaspartase from cell-free extracts of Clostridium tetanomorphum. Optically pure (2S,3S)-3-alkylaspartic acids were transformed in sever
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v