Synthesis of aryl sulfones via L-proline-promoted CuI-catalyzed coupling reaction of aryl halides with sulfinic acid salts
- Author
- WEI ZHU; DAWEI MA
Department of Chemistry, Fudan University, Shanghai 200433, China
State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China - Source
Journal of organic chemistry. 2005, Vol 70, Num 7, pp 2696-2700, 5 p ; ref : 9 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)
- Acide sulfinique Acétanilide Alcool Amine Aminoacide Arène(halogéno) Composé aromatique Copulation chimique Cuivre I Iodure Cétone Ester Groupe fonctionnel Méthyle sulfoxyde Nitrile Proline Réaction catalytique Sulfone Synthèse chimique Phénylalanine dérivé Propionique acide(2-(butoxycarbonylamino)-3-[4-(phénylsulfonyl)phényl]) ester méthyle
- Keyword (en)
- Sulfinic acid Alcohol Amine Aminoacid Haloarene Aromatic compound Chemical coupling Copper I Iodides Ketone Ester Functional group Methyl sulfoxide Nitrile Proline Catalytic reaction Sulfone Chemical synthesis
- Keyword (es)
- Acido sulfínico Alcohol Amina Aminoácido Haloareno Compuesto aromático Copulación química Cobre I Ioduro Cetona Ester Grupo funcional Sulfóxido de dimetilo Nitrilo Prolina Reacción catalítica Sulfona Síntesis química
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C03 Noncondensed benzenic compounds
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 16639767
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/jo047758b 
https://dx.doi.org/10.1021/jo047758b
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