The degradation of toluene‐<sup>14</sup>C

A variety of methods for the preparation of selectively mono-, di-or tri-labelled arenes are reviewed. The review concentrates on those for which the application to labelled synthesis has been demonstrated. Further methods, the application of which to labelled synthesis appears viable but which have not been reduced to practise, are included also. The available methods provide a range of substitution patterns.

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Synthesis of [4,6‐¹³C]nicotinic acid

Barber

1985

Labelled Comp Radiopharmac

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The degradation of toluene‐¹⁴C

Abstract: A method of degradation of toluene-% is described which makes it possible to determine the specific activity of each of the ring carbon atoms.

Cited by 15 publications

References 12 publications

Synthese von 2.4.6‐Tri‐tert.‐butyl‐phenoxyl‐[1‐¹³C]

Synthese von 2.4.6‐Tri‐tert.‐butyl‐phenoxyl‐[1‐¹³C]

Synthetic approaches to regiospecifically mono‐ and dilabelled arenes

Synthesis of [4,6‐¹³C]nicotinic acid

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The degradation of toluene‐14C

Abstract: A method of degradation of toluene-% is described which makes it possible to determine the specific activity of each of the ring carbon atoms.

Cited by 15 publications

References 12 publications

Synthese von 2.4.6‐Tri‐tert.‐butyl‐phenoxyl‐[1‐13C]

Synthese von 2.4.6‐Tri‐tert.‐butyl‐phenoxyl‐[1‐13C]

Synthetic approaches to regiospecifically mono‐ and dilabelled arenes

Synthesis of [4,6‐13C]nicotinic acid

Contact Info

Product

Resources

About

The degradation of toluene‐¹⁴C

Synthese von 2.4.6‐Tri‐tert.‐butyl‐phenoxyl‐[1‐¹³C]

Synthese von 2.4.6‐Tri‐tert.‐butyl‐phenoxyl‐[1‐¹³C]

Synthesis of [4,6‐¹³C]nicotinic acid