MPM (4-methoxybenzyl) protection of hydroxy functions under mild acidic conditions

New Methods for the Synthesis of Glycosides and Oligosaccharides—Are There Alternatives to the Koenigs‐Knorr Method? [New Synthetic Methods (56)]

Richard R. Schmidt · Angewandte Chemie International Edition in English · 1986 · 1.4K citations

Proteinlipid Interaction, Bioorganic Chemistry, Koenigs‐knorr Method +20

Specific removal of o-methoxybenzyl protection by DDQ oxidation.

Yuji Oikawa, Tadao Yoshioka, Osamu Yonemitsu · Tetrahedron Letters · 1982 · 614 citations

Advanced Oxidation Process, Chemical Engineering, Engineering +2

On the selectivity of deprotection of benzyl, mpm (4-methoxybenzyl) and dmpm (3,4-dimethoxybenzyl) protecting groups for hydroxy functions

Kiyoshi Horita, Tadao Yoshioka, Tatsuyoshi Tanaka et al. · Tetrahedron · 1986 · 508 citations

Derivative (Chemistry), Derivatives, Organic Chemistry +4

Benzyl trichloroacetimidate, a versatile reagent for acid-catalysed benzylation of hydroxy-groups

Tommy Iversen, David R. Bundle · Journal of the Chemical Society Chemical Communications · 1981 · 231 citations

Derivative (Chemistry), Engineering, Electrosynthesis +11

A Convenient Benzylation Procedure for β-Hydroxy Esters

Ulrich Widmer · Synthesis · 1987 · 77 citations

Chiral Substrates, Halogenation, Engineering +9