Regioselective ethanolysis of peracylated methyl l3, a-D-glucopyranoside and methyl a-D-mannopyranoside in anhydrous organic solvent (n-hexane/EtOI I L 99/l) could afford 6-OH derivatives exclusively by Can&& rugosu lipase (CRL,). No 4 + 6 acyl migration was observed in such an anhydrous solvent sys
Lipase-catalyzed regioselective protection of hydroxyl groups in aromatic dihydroxyaldehydes and ketones
β Scribed by Giovanni Nicolisi; Mario Piattelli; Claudia Sanfilippo
- Book ID
- 104205012
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- French
- Weight
- 439 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
β¦ Synopsis
Pseudomonas cepacaa ltpase catalyzes the acetylatton m orgamc solvent of dihydroxyaldehydes and ketones using vmyl acetate as acyl donor The method IS completely regoselecuve and allows to obtam partrally acetylated compounds different from those obtamed by enzymic hydrolysis of polyacetoxy arylaldehydes and ketones cepacia Irpase. The authors would also ltke to extend their thanks to MS C Rocco for performmg NMR spectra
π SIMILAR VOLUMES
Comparative Lipase-Catalyzed Hydrolysis of Ethylene Glycol Derived Esters. The 2-Methoxyethyl Ester as a Protective Group in Peptide and Glycopeptide Synthesis. -The 2-methoxyethyl ester group is found to be a potent protecting group in the synthesis of various peptides and glycopeptides. It can be