A Preliminary Approach to Nonenolizable β,β-Tricarbonyls: Assembly of a Hyperevolutin Prototype1
摘要:
A synthetic approach to the h perevolutin A acylated phloroglucinol ring system is described. Thus, intramolecular allene-nitrile oxide cycloaddition of 10 was used to construct the bicyclic framework and vicinal quaternary centers in cycloadduct 20 in the key bond-forming step. Treatment of 20 with Raney nickel and hydrogen gas produced primary enamine 21 which contains a nonenolizable, beta,beta-tricarbonyl group in latent form.
A Preliminary Approach to Nonenolizable β,β-Tricarbonyls: Assembly of a Hyperevolutin Prototype1
摘要:
A synthetic approach to the h perevolutin A acylated phloroglucinol ring system is described. Thus, intramolecular allene-nitrile oxide cycloaddition of 10 was used to construct the bicyclic framework and vicinal quaternary centers in cycloadduct 20 in the key bond-forming step. Treatment of 20 with Raney nickel and hydrogen gas produced primary enamine 21 which contains a nonenolizable, beta,beta-tricarbonyl group in latent form.
A Preliminary Approach to Nonenolizable β,β-Tricarbonyls: Assembly of a Hyperevolutin Prototype<sup>1</sup>
作者:David G. J. Young、Dongxiang Zeng
DOI:10.1021/jo010884k
日期:2002.5.1
A synthetic approach to the h perevolutin A acylated phloroglucinol ring system is described. Thus, intramolecular allene-nitrile oxide cycloaddition of 10 was used to construct the bicyclic framework and vicinal quaternary centers in cycloadduct 20 in the key bond-forming step. Treatment of 20 with Raney nickel and hydrogen gas produced primary enamine 21 which contains a nonenolizable, beta,beta-tricarbonyl group in latent form.