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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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