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Volumn 67, Issue 43, 2011, Pages 8238-8247

Regioselective synthesis of trifluoromethyl group containing allylic amines by palladium-catalyzed allylic amination and sequential isomerization

Author keywords

[No Author keywords available]

Indexed keywords

1 (1,1,1 TRIFLUORO 4 PHENYLBUT 3 EN 2 YL) 4 METHYLPIPERAZINE; 1 (1,1,1 TRIFLUORO 4 PHENYLBUT 3 EN 2 YL) 4 PHENYLPIPERAZINE; 1 (1,1,1 TRIFLUORO 4 PHENYLBUT 3 EN 2 YL) 4 PHENYLPIPERIDINE; 1 (4,4,4 TRIFLUORO 1 PHENYLBUT 2 ENYL) 4 METHYLPIPERAZINE; 1 (4,4,4 TRIFLUORO 1 PHENYLBUT 2 ENYL) 4 PHENYLPIPERAZINE; 1 (4,4,4 TRIFLUORO 1 PHENYLBUT 2 ENYL) 4 PHENYLPIPERIDINE; 1,1,1 TRIFLUORO 4 (4 FLUOROPHENYL)BUT 3 EN 2 YL ACETATE; 1,1,1 TRIFLUORO 4 (4 METHOXYPHENYL)BUT 3 EN 2 YL ACETATE; 1,1,1 TRIFLUORO 4 2 TOLYLBUT 3 EN 2 YL ACETATE; 1,1,1 TRIFLUORO 4 PHENYL N,N DIPROPYLBUT 3 EN 2 AMINE; 1,1,1 TRIFLUORO 4 PHENYLBUT 3 EN 2 YL ACETATE; 4 (1,1,1 TRIFLUORO 4 PHENYLBUT 3 EN 2 YL)MORPHOLINE; 4 (4,4,4 TRIFLUORO 1 PHENYLBUT 2 ENYL)MORPHOLINE; 4,4,4 TRIFLUORO 1 PHENYL N,N DIPROPYLBUT 2 EN 1 AMINE; 4,4,4 TRIFLUORO N ISOPROPYL 1 PHENYLBUT 2 EN 1 AMINE; ALLYL COMPOUND; AMINE; METHYL GROUP; N (4,4,4 TRIFLUORO 1 PHENYLBUT 2 ENYL)BENZENAMINE; N BENZYL 4,4,4 TRIFLUORO 1 PHENYLBUT 2 EN 1 AMINE; N BUTYL 4,4,4 TRIFLUORO 1 PHENYLBUT 2 EN 1 AMINE; N ETHYL 1,1,1 TRIFLUORO N ISOPROPYL 4 PHENYLBUT 3 EN 2 AMINE; N ETHYL 4,4,4 TRIFLUORO N ISOPROPYL 1 PHENYLBUT 2 EN 1 AMINE; N,N DIBUTYL 1,1,1 TRIFLUORO 4 PHENYLBUT 3 EN 2 AMINE; N,N DIBUTYL 4,4,4 TRIFLUORO 1 PHENYLBUT 2 EN 1 AMINE; N,N DIETHYL 1,1,1 TRIFLUORO 4 PHENYLBUT 3 EN 2 AMINE; N,N DIETHYL 4,4,4 TRIFLUORO 1 PHENYLBUT 2 EN 1 AMINE; PALLADIUM; TERT BUTYL 1,1,1 TRIFLUORO 4 PHENYLBUT 3 EN 2 YL CARBONATE; TRIFLUOROMETHYL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 80053052619     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.08.093     Document Type: Article
Times cited : (31)

References (53)
  • 3
    • 36448990108 scopus 로고    scopus 로고
    • For [Pd]
    • Selected examples of transition metal-catalyzed allylic aminations of allylic esters: For [Pd] I. Dubovyk, I.D.G. Watson, and A.K. Yudin J. Am. Chem. Soc. 129 2007 14172
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 14172
    • Dubovyk, I.1    Watson, I.D.G.2    Yudin, A.K.3
  • 47
    • 65249120351 scopus 로고    scopus 로고
    • references therein
    • X.L. Hou, and B.H. Zheng Org. Lett. 11 2009 1789 and references therein
    • (2009) Org. Lett. , vol.11 , pp. 1789
    • Hou, X.L.1    Zheng, B.H.2
  • 48
    • 37049068051 scopus 로고
    • Examples of kinetic resolution in the palladium-catalyzed allylic substitutions of 1,3-disubstituted unsymmetrical allylic esters: T. Hayashi, A. Yamamoto, and Y. Ito J. Chem. Soc., Chem. Commun. 1986 1090
    • (1986) J. Chem. Soc., Chem. Commun. , pp. 1090
    • Hayashi, T.1    Yamamoto, A.2    Ito, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.