Radical and palladium-mediated cyclizations of ortho-iodo benzyl enamines: A scope and limitation study

Synlett

Volumn , Issue 11, 1998, Pages 1227-1230

  Berteina, Sabine ^a   De Mesmaeker, Alain ^a  

^a NOVARTIS PHARMA AG   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0000062386     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1998-1900     Document Type: Article

References (47)

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46. 1H NMR of the crude reaction mixture. After purification by flash chromatography on silica gel (eluent: toluene/AcOEt 85/15), 47 was obtained in 60% yield.
47. 1H NMR of the crude reaction mixture. After purification by flash chromatography on silica gel (eluent: toluene/AcOEt 9/ 1), 47 was isolated in 66% yield.