Takeshi Yamada

Temperature- and ionic strength-induced conformational changes in the lipid head group region of liposomes as suggested by zeta potential data

Kimiko Makino, Takeshi Yamada, Mariko Kimura et al. · Biophysical Chemistry · 1991 · 274 citations

Proteinlipid Interaction, Biochemistry, Protein Folding +6

Michael Addition Reactions between Chiral Equivalents of a Nucleophilic Glycine and (<i>S</i>)- or (<i>R</i>)-3-[(<i>E</i>)-Enoyl]-4-phenyl-1,3-oxazolidin-2-ones as a General Method for Efficient Preparation of β-Substituted Pyroglutamic Acids. Case of Topographically Controlled Stereoselectivity

Vadim A. Soloshonok, Chaozhong Cai, Takeshi Yamada et al. · Journal of the American Chemical Society · 2005 · 86 citations · Full text

Efficient Asymmetric Synthesis of Novel 4-Substituted and Configurationally Stable Analogues of Thalidomide

Takeshi Yamada, Takuya Okada, Kazuhiko Sakaguchi et al. · Organic Letters · 2006 · 86 citations

Design, Synthesis, and Evaluation of a New Generation of Modular Nucleophilic Glycine Equivalents for the Efficient Synthesis of Sterically Constrained α-Amino Acids

Trevor K. Ellis, Hisanori Ueki, Takeshi Yamada et al. · The Journal of Organic Chemistry · 2006 · 85 citations

Combinatorial Chemistry, Medicinal Chemistry, Alpha-amino Acids +14

Application of modular nucleophilic glycine equivalents for truly practical asymmetric synthesis of β-substituted pyroglutamic acids

Vadim A. Soloshonok, Hisanori Ueki, Trevor K. Ellis et al. · Tetrahedron Letters · 2005 · 83 citations

Engineering, Biochemistry, Natural Sciences +7