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Synthesis of a 1,2,7,8-Tetraoxa-spiro[5.5]undecane 被引量:1

Synthesis of a 1,2,7,8-Tetraoxa-spiro[5.5]undecane
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摘要 Synthesis of a new spiro organic peroxide is described. The peroxy bonds were incorporated into the substrate framework via an acid-catalyzed ketal exchange reaction using hydrogen peroxide as the source of peroxy linkage. The hydroperoxyl groups were then bonded at the OH ends via Hg(II)-induced electrophilic additions to the C-C double bonds, giving a novel sprio structure with one peroxy bond in each of the two six-membered rings. The ester functionalities in the side chains also make it possible to conduct further structural modifications. Synthesis of a new spiro organic peroxide is described. The peroxy bonds were incorporated into the substrate framework via an acid-catalyzed ketal exchange reaction using hydrogen peroxide as the source of peroxy linkage. The hydroperoxyl groups were then bonded at the OH ends via Hg(II)-induced electrophilic additions to the C-C double bonds, giving a novel sprio structure with one peroxy bond in each of the two six-membered rings. The ester functionalities in the side chains also make it possible to conduct further structural modifications.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2007年第9期1304-1308,共5页 中国化学(英文版)
基金 Project supported by the National Natural Science Foundation 0f China (Nos. 20025207, 20272071, 20372075, 20321202, 20672129, and 20621062), and the Chinese Academy of Sciences (Nos. NKGCX2-SW-209 and KJCX2.YW.H08).
关键词 PEROXIDE ANTIMALARIAL ARTEMISININ hydrogen peroxide spiro compound peroxide, antimalarial, artemisinin, hydrogen peroxide, spiro compound
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