Pd catalysed intramolecular coupling between tertiary amines and allylic groups ; synthesis of 3-hydro-1H-2-benzazepinium salts
- Author
- GRELLIER, M1 ; PFEFFER, M1 ; VAN KOTEN, G
[1] CNRS Univ. Louis-Pasteur, lab. synthèses métallo-induites, 67070 Strasbourg, France - Source
Tetrahedron letters. 1994, Vol 35, Num 18 ; 2810, 2877-2880 [5 p.]
- CODEN
- TELEAY
- ISSN
- 0040-4039
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Amine tertiaire Ammonium quaternaire composé Cation organique Composé allylique Composé aromatique Composé bicyclique Cyclisation Hétérocycle azote Palladium Complexe Réaction catalytique Réaction intramoléculaire 2-Benzoazépinium(2,3-dihydro-2,2-diméthyl) Prop-2-én-1-ol(1-[2-([diméthylamino] méthyl) phényl]) acétate
- Keyword (en)
- Tertiary amine Quaternary ammonium compound Organic cation Allylic compound Aromatic compound Bicyclic compound Cyclization Nitrogen heterocycle Palladium Complexes Catalytic reaction Intramolecular reaction
- Keyword (es)
- Amina terciaria Amonio cuaternario compuesto Catión orgánico Compuesto alílico Compuesto aromático Compuesto bicíclico Ciclización Heterociclo nitrógeno Paladio Complejo Reacción catalítica Reacción intramolecular
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06B Heterocyclic compounds with only one n hetero atom and condensed derivatives
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4113215
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/S0040-4039(00)76648-2 
https://dx.doi.org/10.1016/S0040-4039(00)76648-2
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