Oxidation of 3β,28-diacetoxy-18-lupen-21-one with peroxy acids : a way to des-E-lupane derivatives
- Author
- KLINOTOVA, E1 ; REJZEK, M1 ; ZUNOVA, H1 ; SEJBAL, J1 ; KLINOT, J1 ; URBAN, J
[1] Charles univ., dep. organic chemistry, 128 40 Prague, Czechoslovakia - Source
Collection of Czechoslovak chemical communications. 1993, Vol 58, Num 10, pp 2505-2516 ; ref : 11 ref
- Publisher
- Czechoslovak Academy of Sciences, Institute of Organic Chemistry and Biochemistry, Praha
- Publication country
- Czech Republic
- Document type
- Article
- Language
- English
- Keyword (fr)
- Acylate Alcool secondaire Alcool tertiaire Catalyse acide Composé pentacyclique Enone Epoxyde Oxydation Peracide organique Triterpène Lup-18-én-21-one(3β,28-diacétoxy) Lupan-21-one(3β,28-diacétoxy-18,19-époxy)
- Keyword (en)
- Acylate Secondary alcohol Tertiary alcohol Acid catalysis Pentacyclic compound Enone Epoxide Oxidation Organic peracid Triterpene
- Keyword (es)
- Acilato Alcohol secundario Alcohol terciario Catálisis ácida Compuesto pentacíclico Enona Epóxido Oxidación Perácido orgánico Triterpeno
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C05 Alicyclic compounds, terpenoids, prostaglandins, steroids / 001C03C05B Terpenoids
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 3961992
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
10.1135/cccc19932505 
https://dx.doi.org/10.1135/cccc19932505
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