N-fluorolactams: Rapid, mild, and regiospecific fluorinating agents

Journal Article · Fri May 11 00:00:00 EDT 1990 · Journal of Organic Chemistry; (United States)

DOI:https://doi.org/10.1021/jo00297a071· OSTI ID:5955511

Satyamurthy, N; Bida, G T; Phelps, M E; Barrio, J R ^[1]

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1. Univ. of California, Los Angeles (United States) Lab. of Nuclear Medicine, Los Angeles, CA (United States)

A method for the synthesis of fluorine-18 labelled N-fluorolactams by reaction with dilute fluorine-18 in freon has been developed. Chemical yields range from 33-79%. Fluorination of a number of Grignard reagents with these fluorolactams has also been achieved, with yields ranging as high as 51%. The reaction of the fluorolactams with Grignard reagents is mild, regiospecific, and facile.

• DOE Contract Number: AC03-76SF00012
• OSTI ID: 5955511
• Journal Information: Journal of Organic Chemistry; (United States), Vol. 55:10; ISSN 0022-3263
• Country of Publication: United States
• Language: English

Related Subjects

37 INORGANIC
ORGANIC
PHYSICAL AND ANALYTICAL CHEMISTRY
GRIGNARD REAGENTS
FLUORINATION
LACTAMS
CHEMICAL PREPARATION
CHEMICAL SHIFT
FLUORINE
FLUORINE 18
FREONS
GAS CHROMATOGRAPHY
NMR SPECTRA
POSITRON COMPUTED TOMOGRAPHY
ALKALINE EARTH METAL COMPOUNDS
AMIDES
BETA DECAY RADIOISOTOPES
BETA-PLUS DECAY RADIOISOTOPES
CHEMICAL REACTIONS
CHROMATOGRAPHY
COMPUTERIZED TOMOGRAPHY
DIAGNOSTIC TECHNIQUES
ELEMENTS
EMISSION COMPUTED TOMOGRAPHY
FLUORINE ISOTOPES
HALOGENATED ALIPHATIC HYDROCARBONS
HALOGENATION
HALOGENS
HOURS LIVING RADIOISOTOPES
ISOMERIC TRANSITION ISOTOPES
ISOTOPES
LIGHT NUCLEI
MAGNESIUM COMPOUNDS
NANOSEC LIVING RADIOISOTOPES
NONMETALS
NUCLEI
ODD-ODD NUCLEI
ORGANIC COMPOUNDS
ORGANIC HALOGEN COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
ORGANOMETALLIC COMPOUNDS
RADIOISOTOPES
SEPARATION PROCESSES
SPECTRA
SYNTHESIS
TOMOGRAPHY
400201* - Chemical & Physicochemical Properties