Momotoshi Okazaki

First enantioselective synthesis of (–)- and (+)-virgatusin, tetra-substituted tetrahydrofuran lignan

Satoshi Yamauchi, Momotoshi Okazaki, Koichi Akiyama et al. · Organic & Biomolecular Chemistry · 2005 · 45 citations

Single Isomer, Tetra-substituted Tetrahydrofuran Lignan, Biochemistry +7

Regulated-Stereoselective Construction of Thirteen Stereogenic Centers Necessary for the Frame of (+)-Discodermolide, Based on Iterative Lewis Acid-Promoted Aldol Reactions

Syun‐ichi Kiyooka, Kazi A. Shahid, Fumitaka Goto et al. · The Journal of Organic Chemistry · 2003 · 34 citations

A straightforward, highly stereoselective construction of eight stereogenic centers in (+)-discodermolide C1–C13 segment, based on a strategy of iterative aldol reactions

Kazi A. Shahid, Jahan Mursheda, Momotoshi Okazaki et al. · Tetrahedron Letters · 2002 · 18 citations

Cross-coupling Reaction, Stereogenic Centers, Engineering +6

Systematic Strategy for the Synthesis of Cyanobacterin and Its Stereoisomers. 1. Asymmetric Total Synthesis of Dechloro-cyanobacterin and Its Enantiomer

Yasushi Haga, Momotoshi Okazaki, Yoshihiro Shuto · Bioscience Biotechnology and Biochemistry · 2003 · 17 citations · Full text

Engineering, Non-chlorinated Analog, Organic Chemistry +16

Total Synthesis of (+)-Phrymarolin I from (+)-Malic Acid

Momotoshi Okazaki, Fumito Ishibashi, Yoshihiro Shuto et al. · Bioscience Biotechnology and Biochemistry · 1997 · 16 citations · Full text

Biochemistry, Natural Sciences, -Malic Acid +10