Stereoselective construction of steroidal trans-hydrindanes via intramolecular ester enolate alkylation [1,2]
- Author
- DEUKJOON KIM; SANGHEE KIM; JAE JEONG LEE; HAK SUNG KIM
Seoul national univ., coll. pharmacy, Kwanak-ku, Seoul 151-742, Korea, Republic of - Source
Tetrahedron letters. 1990, Vol 31, Num 28, pp 4027-4028, 2 p ; ref : 10 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)
- Alkylation Composé bicyclique Composé homoallylique Composé saturé Cétone Dithioacétal Hétérocycle soufre Réaction intramoléculaire Spirane Stéréosélectivité Pent-4-énoïque acide(«2»-méthyl-«3»-[«2»-(«2»-[tosyloxy] éthyl)-«1,3»-dithian-«2»-ylméthyl]) ester éthyle Spiro [«1,3»-dithiane-«2:5p»-indén-«1p»-one](«7a»-méthyl [octahydro])
- Keyword (en)
- Alkylation Bicyclic compound Homoallylic compound Saturated compound Ketone Dithioacetal Sulfur heterocycle Intramolecular reaction Spiran Stereoselectivity
- Keyword (es)
- Alquilación Compuesto bicíclico Compuesto homoalílico Compuesto saturado Cetona Ditioacetal Heterociclo azufre Reacción intramolecular Espirano Estereoselectividad
- 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
- 19380238
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)94490-3 
https://dx.doi.org/10.1016/S0040-4039(00)94490-3
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