Published February 1992 | Version v1
Journal article

Further investigation on the radiosynthesis of α-[11C]methyl-tryptophan

  • 1. Johns Hopkins Medical Institutions, Baltimore, MD (United States)

Description

Improved procedures for the radiosynthesis of α-[11C]-methyl-tryptophan and α-[11C]methyl-tryptophan methyl ester were studied. Following α-deprotonation of tryptophan methyl ester benzaldimine with LDA, 60 - 80% of no carrier added [11C]iodomethane was incorporated in 5 minutes at 27 - 30 oC. After HPLC purification, radiochemically pure α-[11C]methyl-tryptophan or its methyl ester was produced with minimum chemical contamination form tryptophan. The [11C]methyl-tryptophan synthesized, however, was found to be a racemate. (Author)

Additional details

Publishing Information

Journal Title
Journal of Labelled Compounds and Radiopharmaceuticals
Journal Volume
31
Journal Issue
2
Journal Page Range
p. 151-157.
ISSN
0362-4803
CODEN
JLCRD4

Optional Information

Contract/Grant/Project number
Grant USPHS DA 06309; USPHS NS-15080