Masumi Itoh

A new -butyloxycarbonylating reagent, 2--butyloxycarbonyloxyimino-2-phenylacetoni trile.

Masumi Itoh, Daijiro Hagiwara, Takashi Kamiya · Tetrahedron Letters · 1975 · 144 citations

Organic Chemistry, Synthetic Chemistry, Butyloxycarbonyloxyimino-2-phenylacetoni Trile +1

Peptides. VI. Some Oxime Carbonates as Novel <i>t</i>-Butoxycarbonylating Reagents

Masumi Itoh, Daijiro Hagiwara, Takashi Kamiya · Bulletin of the Chemical Society of Japan · 1977 · 99 citations · Full text

I. Selective Protection of α- or Side-chain Carboxyl Groups of Aspartic and Glutamic Acid. A Facile Synthesis of β-Aspartyl and γ-Glutamyl Peptides

Masumi Itoh · Chemical and Pharmaceutical Bulletin · 1969 · 68 citations · Full text

Bioorganic Chemistry, Glutamic Acid, Biochemistry +13

Peptides. IV. Racemization Suppression by the Use of Ethyl 2-Hydroximino-2-cyanoacetate and Its Amide

Masumi Itoh · Bulletin of the Chemical Society of Japan · 1973 · 49 citations · Full text

Diversity Oriented Synthesis, Racemization Suppression, Biochemistry +9

Peptides. II. A New Synthetic Method for the Amino-protected Amino Acid Activated Esters

Masumi Itoh · Chemical and Pharmaceutical Bulletin · 1970 · 23 citations · Full text

New Synthetic Method, Engineering, Biochemistry +11