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Volumn 349, Issue 4-5, 2007, Pages 662-668

Chemoselective palladium-catalyzed reaction in aqueous media: Selectivity in the reaction of haloanilines with 1,1-dimethylallyl alcohol

Author keywords

Allylation; Chemoselectivity; Haloanilines; Palladium; Synthetic methods; Vinylation; water

Indexed keywords


EID: 34547204123     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200600584     Document Type: Article
Times cited : (34)

References (44)
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    • a) J. Muzart, Tetrahedron 2005, 61, 4179-4212, and references cited therein;
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    • Comprehensive review for Heck reaction in aqueous media: I. P. Beletskaya, A. V. Cheprakow, in: Organic Synthesis in Water, (Ed. : P. A. Grieco), Blackie Academic and Professional, London, 1998, Chap. 6, pp. 141-213.
    • Comprehensive review for Heck reaction in aqueous media: I. P. Beletskaya, A. V. Cheprakow, in: Organic Synthesis in Water, (Ed. : P. A. Grieco), Blackie Academic and Professional, London, 1998, Chap. 6, pp. 141-213.
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    • Chem. Abstr. 1996, 180874;
    • Chem. Abstr. 1996, 180874;
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    • We also reported the special property and reactivity of amino acids; a Y. Yokoyama, T. Yamaguchi, M. Sato, E. Kobayashi, Y. Murakami, and H. Okuno, Chem. Pharm. Bull. 2006, 54, 1715-1719;
    • We also reported the special property and reactivity of amino acids; a) Y. Yokoyama, T. Yamaguchi, M. Sato, E. Kobayashi, Y. Murakami, and H. Okuno, Chem. Pharm. Bull. 2006, 54, 1715-1719;
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    • [2a]
    • [2a]
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    • A part of this work was presented at 43rd Symposium on the Chemistry of Natural Products, Osaka, 2001: Y. Yokoyama, H. Hikawa, M. Mitsuhashi, A. Uyama, M. Hiroki, M. Murakami, 43rd Tennen Yuki Kagoubutu Toronkai Koen Yoshisyu (Abstracts Paper) 2001, 539-544.
    • A part of this work was presented at 43rd Symposium on the Chemistry of Natural Products, Osaka, 2001: Y. Yokoyama, H. Hikawa, M. Mitsuhashi, A. Uyama, M. Hiroki, M. Murakami, 43rd Tennen Yuki Kagoubutu Toronkai Koen Yoshisyu (Abstracts Paper) 2001, 539-544.
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    • 2O at 100°C for 3 h.
    • 2O at 100°C for 3 h.
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    • It was reported that 2-iodo-N-allylaniline gave 3-methylindole (32) by intramolecular Heck reaction using these conditions; a) R. Odle, ; B. Blevins; M. Ratcliff; L. S. Hegedus, J. Org. Chem. 1980, 45, 2709-2710;
    • It was reported that 2-iodo-N-allylaniline gave 3-methylindole (32) by intramolecular Heck reaction using these conditions; a) R. Odle, ; B. Blevins; M. Ratcliff; L. S. Hegedus, J. Org. Chem. 1980, 45, 2709-2710;
  • 44
    • 34547196533 scopus 로고    scopus 로고
    • 2 and TPPTS were further added to the mixture from the first reaction, and then aqueous AcOH was added for neutralization. However, the reaction did not proceed.
    • 2 and TPPTS were further added to the mixture from the first reaction, and then aqueous AcOH was added for neutralization. However, the reaction did not proceed.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.