Convenient synthesis of β-silyl ketones from β-stannyl enol silyl ethers via a [1,4] anionic rearrangement of silicon

Hiroyuki Nakahira, Ilhyong Ryu*, Akiya Ogawa, Nobuaki Kambe, Noboru Sonoda

*Corresponding author for this work

Research output: Contribution to journalArticle

6 Scopus citations

Abstract

The transmetalation (Sn to Li) and [1,4] anionic rearrangement of β-stannyl enol silyl ethers have been achieved, providing a convenient method for synthesis of β-silyl ketones.

Original languageEnglish
Pages (from-to)3361-3363
Number of pages3
JournalBulletin of the Chemical Society of Japan
Volume63
Issue number11
DOIs
StatePublished - 1 Nov 1990

Fingerprint Dive into the research topics of 'Convenient synthesis of β-silyl ketones from β-stannyl enol silyl ethers via a [1,4] anionic rearrangement of silicon'. Together they form a unique fingerprint.

  • Cite this