Yutaka Nakazono

On the regioselectivity of the reaction of N-methoxycarbonylpyridinium chloride with Grignard reagents: highly regioselective synthesis of 2-substituted N-methoxycarbonyl-1,2-dihydropyridines.

Ryohei Yamaguchi, Yutaka Nakazono, Mituyosi Kawanisi · Tetrahedron Letters · 1983 · 92 citations

N-methoxycarbonylpyridinium Chloride, Grignard Reagents, Organic Chemistry +5

Highly Regioselective α-Addition of Alkynyl and Alkenyl Grignard Reagents to 1-Alkoxycarbonylpyridinium Salts and Its Application to Synthesis of 1-Azabicycloalkanes and (±)-Solenopsin A

Ryohei Yamaguchi, Yutaka Nakazono, Toshitsugu Matsuki et al. · Bulletin of the Chemical Society of Japan · 1987 · 69 citations · Full text

High α-Regioselectivity, Derivatives, Engineering +15

Synthesis of both the enantiomers of dihydroactinidiolide. a pheromone component of the red imported fire ant

Kenji Mori, Yutaka Nakazono · Tetrahedron · 1986 · 48 citations

Pheromone Biochemistry, Organic Chemistry, Semiochemical +5

Lipase-catalyzed kinetic resolution of methyl 4-hydroxy-5-tetradecynoate and its application to a facile synthesis of japanese beetle pheromone

Eiichiro Fukusaki, Shuji Senda, Yutaka Nakazono et al. · Tetrahedron · 1991 · 39 citations

Biosynthesis, Engineering, Biotransformation +12

Synthesis of both the enantiomers invictolide, a pheromone component of the red imported fire ant

Kenji Mori, Yutaka Nakazono · Tetrahedron · 1986 · 32 citations

Semiochemical, Pheromone Component, Entomology +1