scispace - formally typeset
K

Kazuo Nagasawa

Researcher at Tokyo University of Agriculture and Technology

Publications -  329
Citations -  6484

Kazuo Nagasawa is an academic researcher from Tokyo University of Agriculture and Technology. The author has contributed to research in topics: Enantioselective synthesis & Catalysis. The author has an hindex of 40, co-authored 311 publications receiving 5777 citations. Previous affiliations of Kazuo Nagasawa include Harvard University & University of Tokyo.

Papers
More filters
Journal ArticleDOI

Sequential stereodivergent organocatalysis and programmed organocascades

TL;DR: In this Perspective, the importance of in situ tunability in dynamic asymmetric organocatalysis for obtaining different functional outcomes with single-flask operation is emphasized.
Journal ArticleDOI

A caged ligand for a telomeric G-quadruplex.

TL;DR: The design, synthesis, and characteristics of the first example of a caged compound targeting telomeric G4 are described, which was confirmed to result in inhibition of telomerase activity in vitro and in growth inhibition of several cancer cell lines.
Journal ArticleDOI

Synthesis of Skeletal Analogues of Saxitoxin Derivatives and Evaluation of Their Inhibitory Activity on Sodium Ion Channels NaV1.4 and NaV1.5

TL;DR: Skeletal analogues of saxitoxin (STX) that possess a fused-type tricyclic ring system, designated FD-STX, were synthesized as candidate sodium ion channel modulators, and their inhibitory activity on sodium ion channels was examined by means of cell-based assay.
Journal ArticleDOI

Rif1 promotes association of G-quadruplex (G4) by its specific G4 binding and oligomerization activities.

TL;DR: A model on how Rif1 may facilitate the formation of chromatin architecture through its G4 binding and oligomerization properties is presented.
Journal ArticleDOI

Synthetic study of marine macrolide swinholide A. stereocontrolled synthesis of the C11 - C23 segment

TL;DR: In this paper, the C11-C23 segment of swinholide A was synthesized stereoselectively starting from (S)-malic acid via double nitroaldol reaction under high pressure and differentiation of the left and right parts of the symmetric compound 10 as the key steps.