Novel fragmentation reaction of 2-alkyl- and 2,4-dialkyl-3-iodo-1-oxocyclohexan-2,4-carbolactones
- Author
- KHIM, Seock-Kyu1 ; MINGSHI DAI1 ; XUQING ZHANG1 ; LEI CHEN1 ; PETTUS, Liping1 ; THAKKAR, Kshitij1 ; SCHULTZ, Arthur G1
[1] Department of Chemistiy, Rensselaer Polytechnic Institute, Troy, New York 12180, United States - Source
Journal of organic chemistry. 2004, Vol 69, Num 22, pp 7728-7733, 6 p
- 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)
- Alcoolate Effet stérique Encombrement stérique Fragmentation Hétérocycle oxygène Iode composé organique Lactone Lithium hydroxyde Nucléophile Butyrolactone dérivé Cyclohexanone dérivé Cyclohexènone(4-hydroxy) dérivé Furan-2-one dérivé
- Keyword (en)
- Alkoxide Steric effect Steric hindrance Fragmentation Oxygen heterocycle Organic iodine compounds Lactone Lithium hydroxide Nucleophile
- Keyword (es)
- Alcoholato Efecto estérico Embarazo estérico Fragmentación Heterociclo oxígeno Lactona Litio hidróxido Nucleófilo
- 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
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06A Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 16219232
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/jo0490853 
https://dx.doi.org/10.1021/jo0490853
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