Yuji Kazuta

Development of Versatile <i>cis</i>- and <i>trans</i>-Dicarbon-Substituted Chiral Cyclopropane Units:  Synthesis of (1<i>S</i>,2<i>R</i>)- and (1<i>R</i>,2<i>R</i>)-2-Aminomethyl-1-(1<i>H</i>-imidazol-4-yl)cyclopropanes and Their Enantiomers as Conformationally Restricted Analogues of Histamine

Yuji Kazuta, Akira Matsuda, Satoshi Shuto · The Journal of Organic Chemistry · 2002 · 80 citations

Target Histamine, Enantioselective Synthesis, Heterocyclic +11

Cyclopropane-Based Conformational Restriction of Histamine. (1<i>S</i>,2<i>S</i>)-2-(2-Aminoethyl)-1-(1<i>H</i>-imidazol-4-yl)cyclopropane, a Highly Selective Agonist for the Histamine H₃ Receptor, Having a <i>cis</i>-Cyclopropane Structure

Yuji Kazuta, Kazufumi Hirano, Kentaro Natsume et al. · Journal of Medicinal Chemistry · 2003 · 70 citations · Full text

Construction of a <i>cis</i>-Cyclopropane via Reductive Radical Decarboxylation. Enantioselective Synthesis of <i>cis-</i> and <i>trans-</i>1-Arylpiperazyl-2-phenylcyclopropanes Designed as Antidopaminergic Agents

Kazuya Yamaguchi, Yuji Kazuta, Hiroshi Abe et al. · The Journal of Organic Chemistry · 2003 · 57 citations

Bioorganic Chemistry, Organic Chemistry, Chemistry +16

Stereochemical Diversity-Oriented Conformational Restriction Strategy. Development of Potent Histamine H ₃ and/or H ₄ Receptor Antagonists with an Imidazolylcyclopropane Structure

Mizuki Watanabe, Yuji Kazuta, Hideki Hayashi et al. · Journal of Medicinal Chemistry · 2006 · 56 citations · Full text

A Systematic Study of the Hydride Reduction of Cyclopropyl Ketones with Structurally Simplified Substrates. Highly Stereoselective Reductions of<i>Trans</i>-Substituted Cyclopropyl Ketones via the Bisected<i>s</i>-<i>Cis</i>Conformation

Yuji Kazuta, Hiroshi Abe, Tamotsu Yamamoto et al. · The Journal of Organic Chemistry · 2003 · 31 citations