4-Acetoxy-2-azetidinone

RNA Oligonucleotide Synthesis Via 5-Silyl-2-Orthoester Chemistry

from deoxyribonucleic acid (DNA) synthesis strategies, are limited in their ability to produce oligos of sufficient purity and length for high-throughput applications. The more recently developed 5′-silyl-2′-acetoxy ethyl orthoester chemistry (2′-ACE™), circumvents

Extrachromosomal elements, plasmids, sele

protein that, in the presence of acetyl coenzyme A, catalyzes the formation of hydroxyl acetoxy derivatives of chloramphenicol that are unable to bind to the ribosome. Like with ampicillin , the Cmr gene product destroys the antibiotic