Efficient palladium-catalyzed coupling of Baylis-Hillman acetates with an allylstannane

Synthesis

Volumn , Issue 4, 2010, Pages 661-665

  Park, Jinhyung ^a   Kwon, Young Bum ^a   Yang, Kyungmo ^a   Rhee, Hakjune ^b   Yoon, Cheol Min ^a  

^a Korea University   (South Korea)

^b Hanyang University   (South Korea)

Author keywords

1,5 diene; Allylation; Allyltributylstannane; Baylis Hillman acetates; Bis allylpalladium

Indexed keywords

ALLYLATIONS; ALLYLTRIBUTYLSTANNANE; BAYLIS-HILLMAN ACETATES; BAYLIS-HILLMAN ADDUCTS; CATALYZED COUPLING; ETHYL ACRYLATES; HIGH YIELD; METHYL VINYL KETONES; ROOM TEMPERATURE;

KETONES; OLEFINS; PALLADIUM;

ORGANOMETALLICS;

ACETIC ACID DERIVATIVE; ACRYLIC ACID ETHYL ESTER; ACRYLONITRILE; ALKADIENE; ALLYL COMPOUND; KETONE DERIVATIVE; PALLADIUM; TIN DERIVATIVE; VINYL DERIVATIVE;

ADDITION REACTION; ARTICLE; BAYLIS HILLMAN REACTION; CATALYSIS; CATALYST; CROSS COUPLING REACTION; OXIDATION; QUANTUM YIELD; REACTION ANALYSIS; ROOM TEMPERATURE;

EID: 76249115691     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0029-1218612     Document Type: Article

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