Simple synthesis of deuterium and 13C labeled trifluoromethyl phenyldiazirine derivatives as stable isotope tags for mass spectrometry

13Citations
Citations of this article
10Readers
Mendeley users who have this article in their library.

Abstract

The synthesis of trifluoromethyl diazirine with a stable isotope tag is reported. We found that both Friedel-Crafts acylation and reduction of aryl carbonyl to methylene, using commercially available stable-isotope reagents, were utilized for the synthesis of diazirinyl fatty acid derivatives. The stable isotope labeled diazirine may be valuable for identifying binding sites by mass spectrometry. © 2004 Pharmaceutical Society of Japan.

Cite

CITATION STYLE

APA

Hashimoto, M., & Hatanaka, Y. (2004). Simple synthesis of deuterium and 13C labeled trifluoromethyl phenyldiazirine derivatives as stable isotope tags for mass spectrometry. Chemical and Pharmaceutical Bulletin, 52(11), 1385–1386. https://doi.org/10.1248/cpb.52.1385

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free