118977-96-1Relevant articles and documents
Rapid synthesis of 11C-labeled FK506 for positron emission tomography
Murakami, Yoshihiro,Kuroda, Akio,Osoda, Kazuhiko,Nishimura, Shintaro
, p. 641 - 644 (2003)
The present study describes a rapid synthesis method for labeled [11C]FK506 for positron emission tomography (PET). A one-pot reaction from [11C]CH3I, involving a Wittig reaction as the key carbon-carbon bond formation was developed. The chemical process was accomplished using a designed, fully automated synthetic apparatus, and an injectable solution of [11C]FK506 was obtained in only 34 min from [11C]CH3I. The decay-corrected radiochemical yield based on [11C]CH3I was 11.9%, and the specific activity was 39.8 GBq/μmol.
Total Synthesis of the Immunosuppressant (-)-FK-506
Jones, Todd K.,Mills, Sander G.,Reamer, Robert A.,Askin, D.,Desmond, Richard,et al.
, p. 1157 - 1159 (2007/10/02)
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