857026-03-0

Upstream product

• 857026-02-9 (3-fluoro-1-hydroxymethyl-3-methyl-butyl)-carbamic acid tert-butyl ester 
• 603142-91-2 (4S)-4-(2-fluoro-2-methylpropyl)-1,3-oxazolidin-2-one 
• 13139-15-6 N-tert-butoxycarbonyl-L-leucine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 603142-90-1 (4S)-4-(2-hydroxy-2-methylpropyl)-1,3-oxazolidin-2-one 
• 603142-92-3 (2S)-2-amino-4-fluoro-4-methylpentan-1-ol 

Relevant academic research and scientific papers

Electrostatic Effects Accelerate Decatungstate-Catalyzed C-H Fluorination Using [18F]- And [19F]NFSI in Small Molecules and Peptide Mimics

The site-selective fluorination of unactivated C(sp3)-H bonds provides unique opportunities to rapidly alter drug properties or generate radiotracers for positron emission tomography (PET) imaging. Toward this goal, photoactivated decatungstate

Practical and efficient route to (S)-γ-fluoroleucine

A practical and efficient route to (S)-γ-fluoroleucine was developed via compound 9. Introduction of the fluorine was achieved using N,N-diethylaminosulfur trifluoride (DAST) treatment on a tertiary alcohol 8.