Thallium(III)-mediated allylation of alcohols and carboxylic acids: umpolung of reactivity of allylmetal (group IVb) compounds
- Author
- OCHIAI, M1 ; FUJITA, E; ARIMOTO, M; YAMAGUCHI, H
[1] Kyoto univ., inst. chemical res., Kyoto 611, Japan - Source
Chemical and pharmaceutical bulletin. 1984, Vol 32, Num 12, pp 5027-5030 ; ref : 12 ref
- CODEN
- CPBTAL
- ISSN
- 0009-2363
- Scientific domain
- Organic chemistry; Pharmacology drugs
- Publisher
- Maruzen, Tokyo
- Publication country
- Japan
- Document type
- Article
- Language
- English
- Keyword (fr)
- Acide carboxylique Acétique acide Alcool Allylation Composé aliphatique Composé allylique Composé benzénique Cycle 6 chaînons Cyclisation Etain Composé organique Ethanol Hétérocycle oxygène Inversion polarité Méthanol Réaction intramoléculaire Silicium Composé organique Thallium III Composé Acétique acide,ester alcoxyméthyl-3 butène-3yle Ether(alkyl cinnamyl) Ether(allyl éthyl) Nitrate(cinnamyl) Pyranne(heptyl-2 méthylène-5 perhydro) Silane(allyl triméthyl) Stannane(allyl triméthyl) Thallium III acétate(trifluoro)
- Keyword (en)
- Carboxylic acid Acetic acid Alcohol Allylation Aliphatic compound Allylic compound Benzenic compound Six membered ring Cyclization Tin Organic compounds Ethanol Oxygen heterocycle Polarity inversion Methanol Intramolecular reaction Silicon Organic compounds Thallium III Compounds
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C02 Aliphatic compounds
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 9054208
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
10.1248/cpb.32.5027 
https://dx.doi.org/10.1248/cpb.32.5027
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