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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

CODEN
CCCCAK
ISSN
0010-0765
Scientific domain
Chemistry
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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