- ￥346
- Merck
- 美国
- 8.20234.0025
- 2026年02月13日
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文献和实验Chemical Methods for Peptide-Oligonucleotide Conjugate Synthesis
Methods of peptide-oligonucleotide conjugate synthesis are presented that may be useful in the study of cell targeting and delivery of oligonucleotides and their analogs. The first method involves total stepwise solid-phase synthesis on a single
Detection of Aromatic -Hydroxyketones with Tetrazolium Salts
In principle there are two ways for the biocatalytic synthesis of α-hydroxyketones. Oxidoreductases may be used to convert diketones or diols into the respective α-hydroxyketones. This kind of reaction is exploited, e.g., in the industrial
Cross-Linked Enzyme Aggregates
CLEA for the one-pot synthesis of (S) mandelic acid from benzaldehyde in high yield and enantioselectivity.
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