Racemization in prins cyclization reactions
- Author
- JASTI, Ramesh1 ; RYCHNOVSKY, Scott D1
[1] Department of Chemistry, University of California, Irvine, 1102 Natural Sciences II, Irvine, California 92697-2025, United States - Source
Journal of the American Chemical Society. 2006, Vol 128, Num 41, pp 13640-13648, 9 p ; ref : 32 ref
- CODEN
- JACSAT
- ISSN
- 0002-7863
- Scientific domain
- Biochemistry, molecular biology, biophysics; Chemistry; Organic chemistry; Atomic molecular physics
- Publisher
- American Chemical Society, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Activité optique Etude expérimentale Excès énantiomère Marquage isotopique Mécanisme réaction Nucléophile Pureté optique Racémisation Réaction Prins Solvant Transposition Cope Oxocarbénium composé
- Keyword (en)
- Optical activity Experimental study Enantiomeric excess Isotope labelling Reaction mechanism Nucleophile Optical purity Racemization Prins reaction Solvent Cope rearrangement
- Keyword (es)
- Actividad óptica Estudio experimental Exceso enantiómero Marcación isotópica Mecanismo reacción Nucleófilo Pureza óptica Racemización Reacción Prins Solvente Transposición Cope
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03B Reactivity and mechanisms / 001C03B02 Kinetics and mechanisms
- Discipline
- General chemistry and physical chemistry Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 18193264
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/ja064783l 
https://dx.doi.org/10.1021/ja064783l
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