Synthesis of [ phenyl ‐ 13 C 6 ]lachnanthocarpone and other  13 C‐labelled phenylphenalenones | Zendy

Otálvaro Felipe | Zendy; Quiñones Winston | Zendy; Echeverri Fernando | Zendy; Schneider Bernd | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Synthesis of [ phenyl ‐ 13 C 6 ]lachnanthocarpone and other 13 C‐labelled phenylphenalenones

Author(s) -

Otálvaro Felipe,

Quiñones Winston,

Echeverri Fernando,

Schneider Bernd

Publication year - 2004

Publication title -

journal of labelled compounds and radiopharmaceuticals

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.432

H-Index - 47

eISSN - 1099-1344

pISSN - 0362-4803

DOI - 10.1002/jlcr.808

Subject(s) - chemistry , bromobenzene , stereochemistry , organic chemistry , catalysis

[ 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 methodologies further native phenylphenalenones such as [ phenyl ‐ 13 C 6 ]anigorufone, [1‐ 13 C]anigorufone and [4′‐O 13 CH 3 ]4′‐methoxyanigorufone were synthesized in labelled form. Copyright © 2004 John Wiley & Sons, Ltd.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research