Mild and rapid azide- mediated, palladium catalyzed cleavage of allylester based protecting groups

<i>p</i>-Alkoxybenzyl Alcohol Resin and <i>p</i>-Alkoxybenzyloxycarbonylhydrazide Resin for Solid Phase Synthesis of Protected Peptide Fragments

Su-Sun Wang · Journal of the American Chemical Society · 1973 · 777 citations

Protected Peptide Fragmentssu-sun, Engineering, Peptide Engineering +13

New rules of selectivity: allylic alkylations catalyzed by palladium

Barry M. Trost · Accounts of Chemical Research · 1980 · 630 citations

Asymmetric Catalysis, Altmetrics, Palladiumbarry M. Trostcite +15

Selective cleavage of the allyl and (allyloxy)carbonyl groups through palladium-catalyzed hydrostannolysis with tributyltin hydride. Application to the selective protection-deprotection of amino acid derivatives and in peptide synthesis

Olivier Dangles, F. GUIBE, G.G.A. Balavoine et al. · The Journal of Organic Chemistry · 1987 · 259 citations

Derivative (Chemistry), Engineering, Biochemistry +14

The allylic protection method in solid-phase oligonucleotide synthesis. An efficient preparation of solid-anchored DNA oligomers

Yoshihiro Hayakawa, Shigeharu Wakabayashi, Hisatoyo Kato et al. · Journal of the American Chemical Society · 1990 · 181 citations

Dna Nanotechnology, Solid-phase Oligonucleotide Synthesis, Nucleic Acid Chemistry +15

The allyloxycarbonyl group for alcohol protection: quantitative removal or transformation into allyl protecting group via π-allyl complexes of palladium

F. GUIBE, Y. SAINT M'LEUX · Tetrahedron Letters · 1981 · 155 citations

Cross-coupling Reaction, Allyloxycarbonyl Group, Engineering +6