Rhodium-catalyzed transformation of propargyl alcohol derivatives to 2-silylmethyl-2-alkenals

Isamu Matsuda, Nakayoshi Niikawa, Rika Kuwabara, Hirofumi Inoue, Hideo Nagashima, Kenji Itoh

研究成果: Contribution to journalArticle査読

19 被引用数 (Scopus)

抄録

Propargyl-type alcohols (6) and the corresponding esters of carbonic acid (4) or acetic acid (5) react with two equivalents of Me2PhSiH in the presence of catalytic amounts of Rh4(CO)12 under CO pressure at 100°C to give 2-(dimethylphenylsilylmethyl)-2-alkenals (3), whereas 2-substituted-3-(dimethylphenylsilyl)propenals (7, 8 and 9) are also isolated with the concomitant formation of 3 when a similar reaction is operated with shortage of Me2PhSiH or with lowering of reaction temperature. The isolated 9 is selectively converted to 3 by the Rh4(CO)12 catalyzed reaction with Me2PhSiH under CO pressure. This fact suggests that the transformation of 4, 5 or 6 to 3 is accomplished by either a one-pot procedure or a stepwise procedure relayed by 7, 8 or 9. Usefulness of this protocol is demonstrated by the synthesis of 18 in which ethisterone (17) is directly converted by a one-pot procedure.

本文言語英語
ページ(範囲)133-141
ページ数9
ジャーナルJournal of Organometallic Chemistry
574
1
DOI
出版ステータス出版済み - 2 8 1999

All Science Journal Classification (ASJC) codes

  • 生化学
  • 物理化学および理論化学
  • 有機化学
  • 無機化学
  • 材料化学

フィンガープリント

「Rhodium-catalyzed transformation of propargyl alcohol derivatives to 2-silylmethyl-2-alkenals」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。

引用スタイル