Base-induced rearrangement of 1-trimethylsilylpropargyl alcohol. Generation of lithiated trimethylsiloxyallenes and their reactions

Tetrahedron Letters

Volumn 21, Issue 7, 1980, Pages 623-626

  Kuwajima, Isao ^a   Kato, Masahiro ^a  

^a TOKYO INSTITUTE OF TECHNOLOGY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0000065808     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)85575-1     Document Type: Article

References (14)

1. Reaction of furyllithium with acyltrimethylsilanes. Specific generation of 5-trimethylsiloxy-3,4-pentadienone enolates.
2. 1-Trimethylsilylallylic alcohols as homoenolate precursors. Stereo- and regio-specific synthesis of silyl enol ethers
3. Efficient method for the preparation of trimethylsilyl enol ethers of acyltrimethylsilanes
4. AN EFFICIENT METHOD FOR THE PREPARATION OF ACYLSILANE AND α-HALOACYLSILANE
5. Simple route to mono-, di-, and tri-substituted allenic compounds
6. A new simple stereoselective synthesis of -α, β unsaturated carbonyl compounds.