Deprotection Reagents

Description1H-Imidazole-1-carboxylic acid-3-butenyl ester can be used:To prepare bis-naphthyridine derived cyclic mismatch binding ligands (CMBLs) which exhibit DNA repeat binding properties.As a reagent in the chemoselective esterification of

Description1H-Imidazole-1-carboxylic acid-3-butenyl ester can be used:To prepare bis-naphthyridine derived cyclic mismatch binding ligands (CMBLs) which exhibit DNA repeat binding properties.As a reagent in the chemoselective esterification of

2,5-Hexanedione.

2,5-Hexanedione.

2-(2-Methoxyethoxy)ethyl 2-(chlorosulfonyl)benzoate.

2-(Benzoyloxymethyl)benzoic acid.

2-(Boc-amino)-5-(aminomethyl)pyridine.

2-(Boc-amino)-5-(aminomethyl)pyridine.

DescriptionLearn More at theProfessor and Product Portalof Professor Bruce Lipshutz.Phenol protecting group in the synthesis of laterifluorones.Used to prepare a SEM-ether which was, in turn, removed with BBr3and cyclized to a benzo-oxapane.

DescriptionLearn More at theProfessor and Product Portalof Professor Bruce Lipshutz.Phenol protecting group in the synthesis of laterifluorones.Used to prepare a SEM-ether which was, in turn, removed with BBr3and cyclized to a benzo-oxapane.

DescriptionLearn More at theProfessor and Product Portalof Professor Bruce Lipshutz.Phenol protecting group in the synthesis of laterifluorones.Used to prepare a SEM-ether which was, in turn, removed with BBr3and cyclized to a benzo-oxapane.

DescriptionLearn More at theProfessor and Product Portalof Professor Bruce Lipshutz.Phenol protecting group in the synthesis of laterifluorones.Used to prepare a SEM-ether which was, in turn, removed with BBr3and cyclized to a benzo-oxapane.