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Masayuki Takahashi

Researcher at Scripps Research Institute

Publications -  20
Citations -  648

Masayuki Takahashi is an academic researcher from Scripps Research Institute. The author has contributed to research in topics: RNA & Allylic rearrangement. The author has an hindex of 13, co-authored 20 publications receiving 641 citations. Previous affiliations of Masayuki Takahashi include Yale University.

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Journal ArticleDOI

Monitoring Molecular Recognition of the Ribosomal Decoding Site

TL;DR: An internal loop containing adenine residues A1492 and A1493 in 16S rRNA of the 30S (small) ribosomal subunit constitutes a major component of the bacterial decoding site.
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Solid-phase synthesis of benzimidazole libraries biased for RNA targets

TL;DR: An efficient and highly versatile synthesis of two libraries 1(x,y) and 2-Ar( x,y,z) or 2-R 2 (x,Y,w) based on the privileged benzimidazole scaffold is described, aimed at obtaining molecules biased for binding to RNA targets by incorporating functionalities, which are frequently found in natural RNA-ligands.
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Novel paromamine derivatives exploring shallow-groove recognition of ribosomal-decoding-site RNA.

TL;DR: An in vitro transcription–translation assay of a series of 6‐derivatives showed the 6′‐position to be very sensitive to substitution, which suggests that the group at the 6‐position plays a pivotal role in RNA target recognition.
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Regio- and Stereoselective Cross-Coupling of Substituted Olefins and Imines. A Convergent Stereoselective Synthesis of Saturated 1,5-Aminoalcohols and Substituted Piperidines

TL;DR: A mild and efficient alkoxide-directed C−C bond-forming reaction is described that provides a regio- and stereoselective route to 1,5-aminoalcohols based on cross-coupling of substituted olefins and imines.
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Novel 2,5-dideoxystreptamine derivatives targeting the ribosomal decoding site RNA.

TL;DR: The ribosomal decoding site is the target of aminoglycoside antibiotics that specifically recognize an internal loop RNA structure and RNA-targeted 2,5-dideoxystreptamine-4-amides are synthesized in which a sugar moiety in natural am inoglycosides is replaced by heterocycles.