A novel construction of polyfunctionalised trans-hydroindanes via sulphur-mediated intramolecular double Michael type reaction
- Author
- IHARA, M1 ; SUZUKI, S; TANIGUCHI, N; FUKUMOTO, K; KABUTO, C
[1] Tohoku univ., pharmaceutical inst., Aobayama, Sendai 980, Japan - Source
Journal of the Chemical Society. Chemical communications. 1991, Num 17, pp 1168-1169 ; ref : 7 ref
- CODEN
- JCCCAT
- ISSN
- 0022-4936
- Scientific domain
- Chemistry; Crystallography; Atomic molecular physics
- Publisher
- Royal Society of Chemistry, Cambridge
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Addition Michaël Composé bicyclique Composé saturé Cétoester Cétosulfure Réaction intramoléculaire Stéréoisomère trans Stéréosélectivité Indène-4-carboxylique acide(7-oxo[perhydro]-5-phénylthio) ester méthyle
- Keyword (en)
- Michael addition Bicyclic compound Saturated compound Ketoester Ketosulfide Intramolecular reaction Trans stereoisomer Stereoselectivity
- Keyword (es)
- Adición Michael Compuesto bicíclico Compuesto saturado Cetoester Cetosulfuro Reacción intramolecular Estereoisómero trans 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
- 4999120
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
10.1039/c39910001168 
https://dx.doi.org/10.1039/c39910001168
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