Minako Hashizume

发表

Design , Synthesis , and Structure − Activity Relationships of Novel Pyrazolo [ 5 , 1 ‐ b ] thiazole Derivatives as Potent and Orally Active Corticotropin-Releasing Factor 1 Receptor Antagonists

K. Takeda, M. Ino, Yoshinori Takahashi, 2012 .

Synthesis and structure-activity relationships of 8-substituted-2-aryl-5-alkylaminoquinolines: Potent, orally active corticotropin-releasing factor-1 receptor antagonists.

K. Shikata, K. Takeda, M. Ino, 2012, Bioorganic & medicinal chemistry.

An effective use of benzoic anhydride and its derivatives for the synthesis of carboxylic esters and lactones: a powerful and convenient mixed anhydride method promoted by basic catalysts.

Isamu Shiina, Minako Hashizume, Mari Kubota, 2004, The Journal of organic chemistry.

Synthesis of (9E)-isoambrettolide, a macrocyclic musk compound, using the effective lactonization promoted by symmetric benzoic anhydrides with basic catalysts

Isamu Shiina, Minako Hashizume, 2006 .

Evaluation of the efficiency of the macrolactonization using MNBA in the synthesis of erythromycin A aglycon.

Takashi Katoh, T. Katoh, Isamu Shiina, 2009, Chemical record.

Enantioselective total synthesis of octalactin a using asymmetric aldol reactions and a rapid lactonization to form a medium-sized ring.

Isamu Shiina, Minako Hashizume, Yu-ji Takasuna, 2005, Chemistry.

Enantioselective Total Synthesis of Octalactin A Using Asymmetric Aldol Reactions and a Rapid Lactonization to Form a Medium‐Sized Ring.

Isamu Shiina, Minako Hashizume, Yu-ji Takasuna, 2006 .

Asymmetric total synthesis of octalactin B using a new and rapid lactonization

Isamu Shiina, Minako Hashizume, Hiromi Oshiumi, 2004 .

Design, synthesis, and structure-activity relationships of a series of 2-Ar-8-methyl-5-alkylaminoquinolines as novel CRF₁ receptor antagonists.

K. Takeda, M. Ino, Minako Hashizume, 2012, Bioorganic & medicinal chemistry letters.