hydrolytic cleavage

The hydrolytic cleavage of the silylether gives the acyloin.

The enzyme catalyzes the hydrolytic cleavage of the N-acetamido group in chitin.

Although hydrolytic cleavage is the mildest method, usually the low yields for relatively complicated substrates is a big problem.

Final removal of the peptide from the linkage occurs simultaneously with side-chain deprotection with anhydrous hydrogen fluoride via hydrolytic cleavage.

FENs catalyse hydrolytic cleavage of the phosphodiester bond at the junction of single and double stranded DNA.

A deoxyribonuclease (DNase, for short) is any enzyme that catalyzes the hydrolytic cleavage of phosphodiester linkages in the DNA backbone.

The advantage of this approach is the ability to reduce the amount of hydrolytic cleavage necessary to achieve high enantioselectivity, allowing for overall yields up to approximately 90%, based on the olefin.

The hydrolytic cleavage is irreversible and is considered as an in vitro artefact resulting from a miss-folding of the catalytic site to present the branch nucleotide (BP) correctly for the reaction.

The Na+/K+-ATPase is a P-type pump that extrudes 3Na+ ions in exchange for 2K+ ions for each hydrolytic cleavage of ATP.

P.Rabindra Reddy, Pallerla Manjula and S.Krishna Mohan Novel peptide based copper (II) complexes for total hydrolytic cleavage of DNA.

P. Rabindra Reddy, S. Krishna Mohan, R. Madhusudhan Raju and P. Ettaiah Zinc complexes for hydrolytic cleavage of DNA.

The complex, [κ3-TACN)Cu(II)Cl], a catalyst for hydrolytic cleavage of phosphodiester bonds in DNA, is prepared as follows from TACN trihydrochloride:

Organosolv pulping involves contacting a lignocellulosic feedstock such as chipped wood with an aqueous organic solvent at temperatures ranging from 140-220 C. This causes lignin to break down by hydrolytic cleavage of alpha aryl-ether links into fragments that are soluble in the solvent system.

The characteristic feature of the universal solid supports is that the release of the oligonucleotides occurs by the hydrolytic cleavage of a P-O bond that attaches the 3'-O of the 3'-terminal nucleotide residue to the universal linker as shown in Scheme 6.