A novel chemo-enzymatic synthesis of argininebased gemini cationic surfactants bis(Args) is reported. These compounds consist of two single N ␣ -acyl-arginine structures connected through the alfa-carboxylic groups of the arginine residues by a ␣,-diaminoalkane spacer chain. N ␣ -Acyl-L-arginine alk
Biological properties of arginine-based gemini cationic surfactants
✍ Scribed by Lourdes Pérez; Maria Teresa Garcia; Isabel Ribosa; Maria Pilar Vinardell; Angeles Manresa; Maria Rosa Infante
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 81 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0730-7268
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A novel enzymatic approach for the synthesis of arginine N-alkyl amide and ester derivatives is reported. Papain deposited onto solid support materials was used as catalyst for the amide and ester bond formation between Z-Arg-OMe and various long-chain alkyl amines and alcohols (H 2 N-C n , HO-C n ;
## 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 “Full Text” option. The original article is trackable v
## 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 “Full Text” option. The original article is trackable v