## Abstract [__phenyl__‐^13^C~6~]Lachnanthocarpone ([__phenyl__‐^13^C~6~]2,6‐dihydroxy‐9‐phenylphenalen‐1‐one), a hypothetical intermediate in the biosynthesis of various natural phenylphenalenones, was prepared in four steps using [U‐^13^C]bromobenzene to introduce the label. Based on related meth
A simple synthesis of 13C6-labelled flavone and 5-methoxyflavone
✍ Scribed by Jeffrey J. Ares; Kenneth R. Wehmeyer
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- French
- Weight
- 253 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
The ^13^C~6~‐labelled molecules, flavone and 5‐methoxyflavone, with the carbon‐13 label at all six carbons of the aromatic B ring, have been prepared for use as internal standards in isotope dilution‐mass spectrometry. The key step involves addition of a labelled benzoyl group to the methyl group of a hydroxyacetophenone, forming a 1,3‐diketone. Overall yields from ^13^C~6~‐benzoic acid were 38% for the labelled flavone and 45% for the labelled 5‐methoxyflavone.
📜 SIMILAR VOLUMES
Aniline (IV), specifically 13C labeled in the 4-or in the 3,5-position (IVa and IVb), has been synthesized with 55% yield from I3C labeled pnitrophenol (11). The reduction of the NO2 group and the removal of the OH group was performed in one step by reduction and hydrogenolytic cleavage o f p-nitrop
Pure 3-l-chlorotyrosine-[ring-13 C 6 ] is prepared by chlorination of the 5-oxazolidinone of l-tyrosine-[ring-13 C 6 ] with SO 2 Cl 2 in CH 3 COOH-Et 2 O and successive one-pot regeneration of the protected aminoacidic functions by BCl 3 in dichloromethane.
## Abstract ^3^H‐Sch 58235 was prepared at a specific activity of 29.1 Ci/mmol by Ir(COD)(Cy~3~P)PyPF~6~ catalysed exchange with tritium gas. ^14^C‐Sch 58235 was prepared in three steps from __p__‐hydroxy[ring‐U‐^14^C]benzaldehyde with an overall radiochemical yield of 21%. ^13^C~6~‐Sch 58235 was s