Tautomerism and 1H and 13C NMR assignment of methyl derivatives of 9-hydroxyphenalenone

被引：1

作者：

Honeyman, B

Spalding, C

Jensen, D

Haddon, RC

机构：

[1] Augustana Coll, Dept Chem, Rock Isl, IL 61021 USA

[2] Univ Calif Riverside, Dept Chem, Riverside, CA 92521 USA

[3] Univ Calif Riverside, Dept Environm Chem & Engn, Riverside, CA 92521 USA

来源：

MAGNETIC RESONANCE IN CHEMISTRY | 2005年 / 43卷 / 12期

关键词：

NMR; H-1; C-13; chemical shifts; 9-hydroxyphenalenone;

D O I：

10.1002/mrc.1706

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

9-Hydroxyphenalenone is a planar multicyclic beta-keto-enol that demonstrates C-2v symmetry on the NMR timescale. Off-axis substitution breaks the molecular symmetry and results in tautomers. H-1 and C-13 NMR assignments were made for 9-hydroxyphenalenone and three methyl derivatives, and the solution-phase tautomers were determined. Copyright (c) 2005 John Wiley & Sons, Ltd.

引用

页码：1053 / 1056

页数：4

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