Diastereoselective π-facialy controlled nucleophilic of chiral vinylorgano-metallics to chiral β,γ-unsaturated ketones. II: A practical method for stereocontrolled elaboration of the decahydro-as-indacene subunit of ikarugamycin
- Author
- PAQUETTE, L. A1 ; ROMINE, J. L; LIN, H.-S
[1] Ohio state univ., Evans Chemical Laboratories, Columbus OH 43210, United States - Source
Tetrahedron letters. 1987, Vol 28, Num 1, pp 31-34 ; ref : 15 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)
- Acétal Addition chimique Ammoniac Composé bicyclique Composé insaturé Composé monocyclique Composé tricyclique Cétone Diastéréosélectivité Hydrocarbure bromé Lithium Réaction nucléophile Réduction chimique Cyclopentène(bromo-«2» éthyl-«3» méthyl-«4») Ikarugamycine Indacène dérivé Norbornène-5dione-2,7,diméthylacétal-7
- Keyword (en)
- Acetal Addition reaction Ammonia Bicyclic compound Unsaturated compound Monocyclic compound Tricyclic compound Ketone Diastereoselectivity Bromocarbon Lithium Nucleophilic reaction Chemical reduction
- Keyword (es)
- Acetal Adición química Amoniaco Compuesto bicíclico Compuesto insaturado Compuesto monocíclico Compuesto tricíclico Cetona Diastereoselectividad Hidrocarburo bromado Litio Reacción nucléofila Reducción química
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C05 Alicyclic compounds, terpenoids, prostaglandins, steroids / 001C03C05A Alicyclic compounds
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 8095828
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(00)95641-7 
https://dx.doi.org/10.1016/S0040-4039(00)95641-7
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