Organic reactions catalyzed by insolubilized enzymes; i-peptide synthesis catalyzed by insolubilized α-chymotrypsin
✍ Scribed by D. Salvador; J.V. Sinisterra; J.M. Guisan
- Publisher
- Elsevier Science
- Year
- 1990
- Weight
- 853 KB
- Volume
- 62
- Category
- Article
- ISSN
- 0304-5102
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The synthesis of L-tyrosine glyceryl ester, from glycerol and L-tyrosine methyl ester, was carried out by a transesterification reaction catalyzed by a-chymotrypsin. Values of 60 % (v/v) for glycerol and 200 mM for L-tyrosine methyl ester were optimal for the transesterification reaction. Additional
Aldol reaction of methyl o-isocyanocarboxylates (CNCH(R)aXmc: R -H. Me, Et, i\_Pr)th kntaldehyde or acetaldchyde in the presence of 0.5-1.0 molX of a chiral ~aainoalkyl)ferrocenylphosphine-Sold(I) complex Rave optically active G-methoxycarbonyl-6,5-dialkyl-2-oxszolines with high ensntioaelcctivity i