Palladium catalyzed cyclization-carbonylation of allylic 2-alkynoates : facile synthesis of α-alkylidene-γ-butyrolactone β-acetic acid derivatives
- Author
- JIANGUO JI; XIYAN LU
Chinese acad. sci., Shanghai inst. organic chemistry, Shanghai 200032, China - Source
Tetrahedron (Oxford. Print). 1994, Vol 50, Num 30 ; VII, 9067-9078 [13 p.] ; ref : 18 ref
- CODEN
- TETRAB
- ISSN
- 0040-4020
- Scientific domain
- Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Acide carboxylique Carbonylation Composé énynique Coordinat organique Cycle 5 chaînons Cyclisation Diester Effet milieu Enone Hétérocycle oxygène Lactone Palladium Complexe Réaction catalytique Stéréosélectivité Acide alc-2-ynoïque ester allyle Acide alcanoïque(2-[4-méthoxycarbonylméthyl-2-oxo-perhydro-2-furylidène]) ester méthyle Furane-3-acétique acide(4-[1-chloroalkylidène]-5-oxo-2,3,4,5-tétrahydro])
- Keyword (en)
- Carboxylic acid Carbonylation Enynic compound Organic ligand Five membered ring Cyclization Diester Medium effect Enone Oxygen heterocycle Lactone Palladium Complexes Catalytic reaction Stereoselectivity
- Keyword (es)
- Acido carboxílico Carbonilación Compuesto enínico Ligando orgánico Ciclo 5 eslabones Ciclización Diester Efecto medio Enona Heterociclo oxígeno Lactona Paladio Complejo Reacción catalítica Estereoselectividad
- 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
- 4254890
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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