Dioxopyrrolines. LIII. Stereochemical Pathway of [2 + 2] Photocycloaddition Reaction of 4-Ethoxycarbonyl-5-phenyl-lH-pyrrole-2,3-dione to Cyclic Enol Trimethylsilyl Ethers

Takehiro Sano, Miyuki Hirose, Yoshie Horiguchi, Fumiyuki Kiuchi, Yoshisuke Tsuda

研究成果: Article査読

6 被引用数 (Scopus)

抄録

The photocycladdition reaction of the dioxopyrroline 1 to cyclic trimethylsilyloxy olefins was examined. The addition of 3-trimethylsilyloxy-lH-indene and 4-trimethylsilyloxy-l,2-dihydronaphthalene occurred in a regio- and stereoselective manner to give the cis-anti-cis cyclobutanes 3 and 4, respectively. The stereochemical result supported the stereo-selection rule which states that the photocycloaddition of a very polar dioxopyrroline-olefin pair proceeds in an s + s manner via a favored O-endo-π-complex transition. On the other hand, the addition of 1-trimethylsilyloxycyclopentene and l-trimethylsily!oxycyclohexene occurred less stereoselectively, proceeding predominantly in an s + a manner to give the adducts 5a, b, 6a, b, 7a, b, and 12. The results are consistent with the prediction of the stereo-selection rule obtained by assuming that these dioxopyrroline-olefin pairs are polar. The latter cases demonstrate that an increased steric hindrance around the olefin moiety affects the polarity of enone-olefin pair in the transition state.

本文言語English
ページ(範囲)64-72
ページ数9
ジャーナルChemical and Pharmaceutical Bulletin
41
1
DOI
出版ステータスPublished - 1993 1月 1
外部発表はい

ASJC Scopus subject areas

  • 化学 (全般)
  • 創薬

フィンガープリント

「Dioxopyrrolines. LIII. Stereochemical Pathway of [2 + 2] Photocycloaddition Reaction of 4-Ethoxycarbonyl-5-phenyl-lH-pyrrole-2,3-dione to Cyclic Enol Trimethylsilyl Ethers」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

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