Facile synthesis of diazido-functionalized biaryl compounds as radioisotope-free photoaffinity probes by Suzuki-Miyaura coupling

Bioorganic and Medicinal Chemistry

Volumn 17, Issue 6, 2009, Pages 2490-2496

  Hosoya, Takamitsu ^a   Inoue, Atsushi ^a   Hiramatsu, Toshiyuki ^a   Aoyama, Hiroshi ^b   Ikemoto, Takaaki ^c   Suzuki, Masaaki ^c  

^a TOKYO INSTITUTE OF TECHNOLOGY   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

^c RIKEN   (Japan)

Author keywords

Dantrolene; Photoaffinity labeling; Radioisotope free; Suzuki Miyaura coupling

Indexed keywords

3 AZIDO 5 (AZIDOMETHYL)PHENYLBORONIC ACID PINACOL ESTER; AZIDE; CALCIUM ION; DANTROLENE; DANTROLENE DERIVATIVE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; UNCLASSIFIED DRUG;

ANIMAL TISSUE; ARTICLE; CALCIUM TRANSPORT; CHEMICAL STRUCTURE; MOUSE; NONHUMAN; PHOTOAFFINITY LABELING; REACTION ANALYSIS; SARCOPLASMIC RETICULUM; STRUCTURE ANALYSIS; SUZUKI MIYAURA COUPLING REACTION; SUZUKI REACTION; SYNTHESIS;

AZIDES; CALCIUM; MAGNETIC RESONANCE SPECTROSCOPY; PHOTOAFFINITY LABELS; RADIOISOTOPES; SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION; SPECTROMETRY, MASS, FAST ATOM BOMBARDMENT;

EID: 62549144399     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2009.01.070     Document Type: Article

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