Total synthesis of (-)-laurenyne: use of acetal-initiated cyclizations to prepare functionalized eight-membered cyclic ethers
- Author
- OVERMAN, L. E1 ; THOMPSON, A. S
[1] Univ. California, dep. chemistry, Irvine CA 92717, United States - Source
Journal of the American Chemical Society. 1988, Vol 110, Num 7, pp 2248-2256 ; ref : 50 ref
- CODEN
- JACSAT
- ISSN
- 0002-7863
- Scientific domain
- Biochemistry, molecular biology, biophysics; Chemistry; Organic chemistry; Atomic molecular physics
- Publisher
- American Chemical Society, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Acétal Composé aliphatique Composé énynique Cycle 8 chaînons Cyclisation Enantiomère(-) Hétérocycle oxygène Spectre IR Spectre RMN Spectre masse Butanal(t-butyldiphénylsiloxy-«4»)[(chloro-«2p» tosyloxyméthyl-«1p» triméthylsilyl-«5p») hexène-«5p» yl éthyl] acétal Carbone 13 Hydrogène 1 Laurényne Oxocinne dérivé
- Keyword (en)
- Acetal Aliphatic compound Enynic compound Eight membered ring Cyclization Enantiomer(-) Oxygen heterocycle Infrared spectrum NMR spectrum Mass spectrum
- Keyword (es)
- Acetal Compuesto alifático Compuesto enínico Ciclo 8 eslabones Ciclización Enantiómero(-) Heterociclo oxígeno Espectro IR Espectro de RMN Espectro masa
- 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
- 7585384
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
10.1021/ja00215a040 
https://dx.doi.org/10.1021/ja00215a040
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