The palladium(0) Suzuki cross-coupling reaction as the key step in the synthesis of aporphinoids

Tetrahedron

Volumn 60, Issue 27, 2004, Pages 5725-5735

  Suau, R ^a   Rico, R ^a   Najera F ^a   Ortiz Lopez F J ^a   Lopez Romero J M ^a   Moreno Manas M ^b   Roglans, A ^b  

^a UNIVERSITY OF MÁLAGA   (Spain)

^b UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

Author keywords

4,5 Dioxoaporphine; 4 Hydroxy dehydroaporphine; Apomorphine; Aporphine; Aporphinoids; Cascade cyclization; Oxalyl chloride; Palladium; Reduction; Suzuki cross coupling

Indexed keywords

ACETAMIDE DERIVATIVE; APORPHINE DERIVATIVE; BENZENEBORONIC ACID; LEWIS ACID; PALLADIUM; PHENYLACETIC ACID DERIVATIVE;

ARTICLE; CYCLIZATION; PRIORITY JOURNAL; SUZUKI REACTION; SYNTHESIS;

LATEOLABRAX JAPONICUS;

EID: 2942521185     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.05.014     Document Type: Article

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