Palladium catalysed cross-coupling of vinyl triflates with 9-alkyl-9-borobicyclo[3,3,1]nonanes. Total synthesis of (-)-isoseiridine
- Author
- GRIGG, R1 ; KENNEWELL, P; SAVIC, V1
[1] Leeds univ., school chemistry, Leeds LS29 JT, United Kingdom - Source
Tetrahedron (Oxford. Print). 1994, Vol 50, Num 18 ; IX, 5489-5494 [7 p.] ; ref : 13 ref
- CODEN
- TETRAB
- ISSN
- 0040-4020
- Scientific domain
- Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Alcool secondaire Copulation chimique Cycle 5 chaînons Enantiomère Enone Furane dérivé Hétérocycle oxygène Lactone Palladium Phytotoxine Réaction catalytique Réaction croisée Synthèse totale 1,3-Dioxolane(2-[but-3-ényl]) 9-Borabicyclo [3.3.1] nonane Furan-2-one(2,5-dihydro-3-méthyl-4-trifluoromésyloxy) Isoseiridine
- Keyword (en)
- Secondary alcohol Chemical coupling Five membered ring Enantiomer Enone Furan derivatives Oxygen heterocycle Lactone Palladium Phytotoxin Catalytic reaction Cross reaction Total synthesis
- Keyword (es)
- Alcohol secundario Copulación química Ciclo 5 eslabones Enantiómero Enona Furano derivado Heterociclo oxígeno Lactona Paladio Fitotoxina Reacción catalítica Reacción cruzada 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
- 4065467
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
10.1016/S0040-4020(01)80703-1 
https://dx.doi.org/10.1016/S0040-4020(01)80703-1
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