Palladium-catalyzed C-allylation of naphthols by direct use of allylic alcohols under neutral conditions

Chemistry Letters

Volumn , Issue 12, 1996, Pages 1021-1022

  Tada, Yuzuki ^a   Satake, Akiharu ^a   Shimizu, Isao ^a   Yamamoto, Akio ^a  

^a WASEDA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0042103128     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.1996.1021     Document Type: Article

References (24)

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15. 3.
16. M. Sakamoto, I. Shimizu, and A. Yamamoto, Bull. Chem. Soc. Jpn., 69, 1065 (1996). Some papers concerning palladium-catalyzed allylation with allylic alcohols have been reported. These references are cited in this paper.
17. 2 is converted into zero valent palladium species by alkyl-or arylphosphine and water: a) F. Ozawa, A. Kubo, and T. Hayashi, Chem. Lett., 1992, 2177.
18. b) C. Amatore, A. Jutand, and M. A. M'Barki, Organometallics, 11, 3009 (1992).
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23. Dihydroxynaphthalene 22 is insoluble in toluene.
24. 3, 67.9 MHz) δ 203.5, 152.4. 141.3, 136.7, 135.8, 132.7, 130.3, 126.1, 126.0, 123.7, 117.9, 117.4, 116.0, 55.6, 46.5, 28.9.