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  • Lipase-catalyzed enantioselective transesterification of prochiral 1-((1,3-dihydroxypropan-2-yloxy)methyl)-5,6,7,8-tetrahydroquinazoline-2,4(1H,3H)-dione in ionic liquids.

Lipase-catalyzed enantioselective transesterification of prochiral 1-((1,3-dihydroxypropan-2-yloxy)methyl)-5,6,7,8-tetrahydroquinazoline-2,4(1H,3H)-dione in ionic liquids.

Chirality (2017-11-16)
Renata Kołodziejska, Renata Studzińska, Hanna Pawluk
ABSTRACT

The application of ionic liquids as solvents for transesterification of prochiral pirymidine acyclonucleoside using lipase (EC 3.1.1.3) Amano PS from Burkholderia cepacia (BCL) is reported. The effect of using medium reaction, acyl group donor, and temperature on the activity and enantioselectivity of BCL was studied. From the investigated ionic solvents, the hydrophobic ionic liquid [BMIM]PF

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Sigma-Aldrich
1,3-Propylene sulfite, 99%
Sigma-Aldrich
Vinyl butyrate, contains 20 ppm 4-methoxyphenol as stabilizer, ≥99.0% (GC)
Sigma-Aldrich
1-Hexyl-3-methylimidazolium tetrafluoroborate, ≥97.0% (HPLC)