On the occurrence of the 1,3,5-trisubstitution pattern in the O-alkylation of p-tert-butylcalix[6]arene
- Author
- NERI, P; CONSOLI, G. M. L; CUNSOLO, F; PIATTELLI, M
CNR, ist. studio sostanze naturali interesse alimentare chimico-farmaceutico, 95028 Valverde, Italy - Source
Tetrahedron letters. 1994, Vol 35, Num 17 ; 2633, 2795-2798 [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)
- Alkylation Calixarène Composé polycyclique Cyclophane Césium Fluorure Ether Macrocycle Potassium Carbonate Réaction catalytique Régiosélectivité Spectre RMN Substitution électrophile Hydrogène 1 [1.6] Métacyclophane(hexa-t-butyl hexahydroxy) [1.6] Métacyclophane(hexa-t-butyl trialcoxytrihydroxy)
- Keyword (en)
- Alkylation Calixarene Polycyclic compound Cyclophane Cesium Fluorides Ether Macrocycle Potassium Carbonates Catalytic reaction Regioselectivity NMR spectrum Electrophilic substitution
- Keyword (es)
- Alquilación Calixareno Compuesto policíclico Ciclofano Cesio Fluoruro Eter Macrociclo Potasio Carbonato Reacción catalítica Regioselectividad Espectro de RMN Sustitución electrófila
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C05 Alicyclic compounds, terpenoids, prostaglandins, steroids / 001C03C05A Alicyclic compounds
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4054100
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)77035-3 
https://dx.doi.org/10.1016/S0040-4039(00)77035-3
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