Synthesis of nitrocyclopentanes via a 3 + 2 strategy
- Author
- GHERA, E; YECHEZKEL, T; HASSNER, A
Bar-Ilan univ., dep. chemistry, Ramat Gan 52900, Israel - Source
Journal of organic chemistry. 1993, Vol 58, Num 24, pp 6716-6724 ; ref : 24 ref
- CODEN
- JOCEAH
- ISSN
- 0022-3263
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- American Chemical Society, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Addition Michaël Composé monocyclique Composé éthylénique Cyclisation Réaction intramoléculaire Réaction tandem Stéréosélectivité But-1-ène(1-nitro) Styrène(β-nitro) Sulfone(2-[bromométhyl]allyl phényl) Sulfone(2-aryl-5-méthylène-3-nitrocyclopentyl phényl) Sulfone(2-éthyl-5-méthylène-3-nitrocyclopentyl phényl)
- Keyword (en)
- Michael addition Monocyclic compound Ethylenic compound Cyclization Intramolecular reaction Tandem reaction Stereoselectivity
- Keyword (es)
- Adición Michael Compuesto monocíclico Compuesto etilénico Ciclización Reacción intramolecular Reacción tándem 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
- 3817189
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/jo00076a035 
https://dx.doi.org/10.1021/jo00076a035
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