| Literature DB >> 17117852 |
Hiroyuki Nakashima1, Makoto Hashimoto, Yutaka Sadakane, Takenori Tomohiro, Yasumaru Hatanaka.
Abstract
The first effective method for the introduction of a versatile substituent on 3-phenyl-3-trifluoromethyldiazirine has been developed. The simple preparation of a useful aldehyde intermediate allows easy access to various elaborated photoaffinity ligands, including a l-phenylalanine analog bearing a diazirine ring (TmdPhe). The asymmetric synthesis of TmdPhe was easily accomplished in gram quantities. Site-directed incorporation of this compound into the structure of a calmodulin-binding peptide using automated peptide synthesis afforded a photoreactive peptide that was successfully used for the specific labeling of calmodulin.Entities:
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Year: 2006 PMID: 17117852 DOI: 10.1021/ja066479y
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419