Synthesis of the enantiomeric furobenzofurans, late precursors for the synthesis of (+)- and (-)-aflatoxins B1, B2, G1, and G2
- Author
- CIVITELLO, E. R; RAPOPORT, H
Univ. California, dep. chemistry, Berkeley CA 94720, United States - Source
Journal of organic chemistry. 1994, Vol 59, Num 14, pp 3775-3782 ; ref : 12 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)
- Aldoxime Composé aromatique Composé tricyclique Cyclisation Enantiosélectivité Hétérocycle oxygène Réaction électrochimique Réduction chimique Régiosélectivité Transposition chimique Benzofurane-3-propionique acide(α-benzyloxy-2,3-dihydro-4,6-ditosyloxy-2-méthoxy) ester méthyle Furo[2,3-b]benzofurane dérivé Valérique acide(2-benzyloxy-5-[(3,5-ditosyloxyphénoxy)imino]) ester méthyle
- Keyword (en)
- Aldoxime Aromatic compound Tricyclic compound Cyclization Enantioselectivity Oxygen heterocycle Electrochemical reaction Chemical reduction Regioselectivity Chemical rearrangement
- Keyword (es)
- Aldoxima Compuesto aromático Compuesto tricíclico Ciclización Enantioselectividad Heterociclo oxígeno Reacción electroquímica Reducción química Regioselectividad Transposición química
- 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
- 4139129
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/jo00093a008 
https://dx.doi.org/10.1021/jo00093a008
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