Reductive cleavage methods, such as borane or lithium aluminum hydride (LiAlH4) reduction, can be used to break specific peptide bonds. This can be useful in the synthesis of peptides with disulfide bridges, where protecting groups and selective cleavage are necessary.
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2-Formylamino-N-(N'-phenyl-hydrazinocarbonylmethyl)-acetamide
2-(1,1-Dioxo-2,3-dihydro-1H-1λ6-thiophen-3-yl)-phenol
1,2,4-Triazine, 3-(2-chlorophenoxy)-5,6-diphenyl-
2-Butanol, 1-(phenyltelluro)-
2,2,6,6-TETRAMETHYLPIPERIDINE HYDROBROMIDE
2-[2-(2-Thienyl)ethyl]benzoic acid
(8S,23S,25R)-de-A,B-8-(benzyloxy)cholestan-23,25,26-triol
1,2-bis(4-chlorophenyl)-2-oxoethyl acetate
phenyl 3-O-(tert-butyldimethylsilyl)-4-O-(p-methoxybenzyl)-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside
methyl (phenylseleno)formate
methyl 2,3,4-tri-O-benzyl-α-D-mannopyranoside
5,5-dimethyl-2-pyrrolidone
