Synthesis of intermediates for the lactone moiety of mevinic acids via tellurium chemistry
- Author
- ARCHANA KUMAR; DITTMER, D. C
Syracuse univ., cent. sci. technology, dep. chemistry, Syracuse NY 13244, United States - Source
Journal of organic chemistry. 1994, Vol 59, Num 17, pp 4760-4764
- 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)
- Alcool secondaire Cycle 6 chaînons Epoxyde Hydroxyester Hétérocycle oxygène Lactone Réaction asymétrique Tellure Hept-6-énoïque acide(3-[t-butyldiméthylsiloxy]-5-hydroxy) ester t-butyle Méthanesulfinate(hydroxy) Oxirane-2-butyrique acide(β-[t-butyldiphénylsiloxy]-3-tosyloxy) ester méthyle Pyran-2-one(4-[t-butyldiméthylsiloxy]-perhydro-6-vinyl)
- Keyword (en)
- Secondary alcohol Six membered ring Epoxide Hydroxyester Oxygen heterocycle Lactone Asymmetric reaction Tellurium
- Keyword (es)
- Alcohol secundario Ciclo 6 eslabones Epóxido Hidroxiester Heterociclo oxígeno Lactona Reacción asimétrica Teluro
- Classification
- 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
- 4184320
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/jo00096a017 
https://dx.doi.org/10.1021/jo00096a017
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