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Stereoselective synthesis of tetrahydrofurans via formal [3+2]-cycloaddition of aldehydes and allylsilanes. Formal total synthesis of the muscarine alkaloids (-)-allomuscarine and (+)-epimuscarine

Author
ANGLE, Steven R1 ; EL-SAID, Nahla A1
[1] Department of Chemistry, University of California-Riverside, Riverside, California 92521-0403, United States
Source

Journal of the American Chemical Society. 2002, Vol 124, Num 14, pp 3608-3613

CODEN
JACSAT
ISSN
0002-7863
Scientific domain
Biochemistry, molecular biology, biophysics; Chemistry; Organic chemistry; Atomic molecular physics
Publisher
American Chemical Society, Washington, DC
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Alcaloïde Ammonium quaternaire composé Cycle 5 chaînons Cycloaddition dipolaire Diastéréosélectivité Furane dérivé Hétérocycle oxygène Synthèse totale Allomuscarine Epimuscarine Réaction Fleming Tamao
Keyword (en)
Alkaloid Quaternary ammonium compound Five membered ring Dipolar cycloaddition Diastereoselectivity Furan derivatives Oxygen heterocycle Total synthesis
Keyword (es)
Alcaloide Amonio cuaternario compuesto Ciclo 5 eslabones Cicloadición dipolar Diastereoselectividad Furano derivado Heterociclo oxígeno Síntesis total
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
13603263

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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