Total syntheses of (±)-cephalotaxine and (±)-8-oxocephalotaxine
- Author
- KUEHNE, M. E1 ; BORNMANN, W. G; PARSONS, W. H; SPITZER, T. D; BLOUNT, J. F; ZUBIETA, J
[1] Univ. Vermont, dep. chemistry, Burlington VT 05405, United States - Source
Journal of organic chemistry. 1988, Vol 53, Num 15, pp 3439-3450 ; ref : 70 ref
- 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)
- Alcaloïde Anticancéreux Composé aromatique Composé pentacyclique Hétérocycle oxygène azote Lactame Oxydation Racémique Spirane Transposition chimique Aza-«1»spiro [«4.4»] nonanedione-2,6([benzodioxole-«1,3»yl-«5»]-«2p» éthyl-«1») Cyclopenta dioxolo pyrrolo benzazépine dérivé Céphalotaxine(oxo-8) Céphalotaxine Pyrindine-«1»one-2([benzodioxole-«1,3»yl-«5»]-«2p» éthyl-«1» hexahydro)
- Keyword (en)
- Alkaloid Antineoplastic agent Aromatic compound Pentacyclic compound Oxygen nitrogen heterocycle Lactam Oxidation Racemate Spiran Chemical rearrangement
- Keyword (es)
- Alcaloide Anticanceroso Compuesto aromático Compuesto pentacíclico Heterociclo oxígeno nitrógeno Lactamo Oxidación Racémico Espirano Transposición química
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06D Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 7291161
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/jo00250a008 
https://dx.doi.org/10.1021/jo00250a008
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