Mari Nakatani

Chiral Amine-Catalyzed Asymmetric Baylis<i>−</i>Hillman Reaction:  A Reliable Route to Highly Enantiomerically Enriched (α-Methylene-β-hydroxy)esters

Yoshiharu Iwabuchi, Mari Nakatani, N. Yokoyama et al. · Journal of the American Chemical Society · 1999 · 407 citations

Highly Enantiomerically Enriched, Engineering, Organic Chemistry +8

β-Isocupreidine–hexafluoroisopropyl acrylate method for asymmetric Baylis–Hillman reactions

Ayako Nakano, Sakie Kawahara, Saori Akamatsu et al. · Tetrahedron · 2005 · 87 citations

β-Isocupreidine–hexafluoroisopropyl Acrylate Method, Organic Chemistry, Chemistry +2

An efficient synthesis of (+)-aureol via boron trifluoride etherate-promoted rearrangement of (+)-arenarol

Masahiko Nakamura, Akiyuki Suzuki, Mari Nakatani et al. · Tetrahedron Letters · 2002 · 51 citations

Cross-coupling Reaction, Engineering, Alkene Metathesis +9

Stable axial-rich conformation of pyranoses derived from L-rhamnose and D-mannose

Hidetoshi Yamada, Mari Nakatani, Tomonari Ikeda et al. · Tetrahedron Letters · 1999 · 47 citations

Bioorganic Chemistry, Engineering, Biochemistry +6

A New Strategy toward the Total Synthesis of Stachyflin, A Potent Anti-Influenza A Virus Agent:  Concise Route to the Tetracyclic Core Structure

Mari Nakatani, Masahiko Nakamura, Akiyuki Suzuki et al. · Organic Letters · 2002 · 45 citations

Combinatorial Chemistry, Medicinal Chemistry, Tetracyclic Core Structure +14