Diastereoselectivity in the directed aldol condensation of 2-trimethylsiloxyfuran with aldehydes. A stereodivergent route to threo and erythro δ-hydroxy-γ-lactones
- Author
- JEFFORD, C. W1 ; JAGGI, D; BOUKOUVALAS, J
[1] Univ. Geneva, dep. organic chemistry, Geneva 1211, Switzerland - Source
Tetrahedron letters. 1987, Vol 28, Num 35, pp 4037-4040 ; ref : 21 ref
- CODEN
- TELEAY
- ISSN
- 0040-4039
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Aldolisation Aldéhyde Cycle 5 chaînons Diastéréosélectivité Hétérocycle oxygène Lactone Silicium Composé organique Furanne(triméthylsiloxy-2) Furannone-2(dihydro-«2,5» hydroxy-«1p» hexyl-«5») Furannone-2(«α»-hydroxyphénéthyl-«5» perhydro) Hexanal
- Keyword (en)
- Aldol condensation Aldehyde Five membered ring Diastereoselectivity Oxygen heterocycle Lactone Silicon Organic compounds
- Keyword (es)
- Aldolización Aldehido Ciclo 5 eslabones Diastereoselectividad Heterociclo oxígeno Lactona Silicio
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06A Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 8314229
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1016/S0040-4039(01)83855-7 
https://dx.doi.org/10.1016/S0040-4039(01)83855-7
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