Abstract
Lithium butatrienolates were prepared in situ by the 1,4-elimination from 2-butynyl trimethylsilyl ethers along with a retro-Brook rearrangement. The addition reaction of the enolates with the aldehydes afforded β-hydroxy-α-vinyl-idene acylsilanes.
Original language | English |
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Pages (from-to) | 1937-1938 |
Number of pages | 2 |
Journal | Bulletin of the Chemical Society of Japan |
Volume | 77 |
Issue number | 10 |
DOIs | |
Publication status | Published - 2004 Oct |
ASJC Scopus subject areas
- Chemistry(all)