Tetrahedron Letters

A synthesis of the abietane diterpenoid quinone (±)-royleanone via maleoylcobalt technology.

LS Liebeskind, R Chidambaram, S Nimkar, D Liotta

Index: Liebeskind; Chidambaram; Nimkar; Liotta Tetrahedron Letters, 1990 , vol. 31, # 26 p. 3723 - 3726

Full Text: HTML

Citation Number: 12

Abstract

Abstract (±)-Royleanone has been synthesized by rapid construction of a highly substituted quinone using maleoylcobalt complex technology followed by acid induced cyclization of the corresponding hydroquinone methyl ether onto a tethered enone. The synthesis was completed by straightforward functional group manipulations.

Related Articles:

A strategy for generalization of the regiospecific synthesis of substituted quinones from cyclobutenediones

[Liebeskind, Lanny S.; Granberg, Kenneth L.; Zhang, Jing Journal of Organic Chemistry, 1992 , vol. 57, # 16 p. 4345 - 4352]

More Articles...