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Volumn 130, Issue 13, 2008, Pages 4492-4496

Construction of a chiral quaternary carbon center by indium-catalyzed asymmetric α-alkenylation of β-ketoesters

Author keywords

[No Author keywords available]

Indexed keywords

ALKYLATION; CATALYST ACTIVITY; CHIRALITY; ESTERS; INDIUM COMPOUNDS;

EID: 41549124113     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja710408f     Document Type: Article
Times cited : (74)

References (43)
  • 10
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    • Recently transition metal-catalyzed Conia-ene type alkenylation reactions have been reported. (a) Au catalysis: Kennedy-Smith, J. J.; Staben, S. T.; Toste, F. D. J. Am. Chem. Soc. 2004, 126, 4526-4527.
    • Recently transition metal-catalyzed Conia-ene type alkenylation reactions have been reported. (a) Au catalysis: Kennedy-Smith, J. J.; Staben, S. T.; Toste, F. D. J. Am. Chem. Soc. 2004, 126, 4526-4527.
  • 11
    • 33845959705 scopus 로고    scopus 로고
    • Au catalysis: Ochida, A.; Ito, H.; Sawamura, M. J. Am. Chem. Soc. 2006, 128, 16486-16487.
    • (b) Au catalysis: Ochida, A.; Ito, H.; Sawamura, M. J. Am. Chem. Soc. 2006, 128, 16486-16487.
  • 12
    • 27644479913 scopus 로고    scopus 로고
    • Re catalysis: Kuninobu, Y.; Kawata, A.; Takai, K. Org. Lett. 2005, 7, 4823-4825.
    • (c) Re catalysis: Kuninobu, Y.; Kawata, A.; Takai, K. Org. Lett. 2005, 7, 4823-4825.
  • 13
    • 20444465253 scopus 로고    scopus 로고
    • Ni/Yb catalysis: Gao, Q.; Zheng, B.-F.; Li, J.-H.; Yang, D. Org. Lett. 2005, 7, 2185-2188.
    • (d) Ni/Yb catalysis: Gao, Q.; Zheng, B.-F.; Li, J.-H.; Yang, D. Org. Lett. 2005, 7, 2185-2188.
  • 14
    • 0001521888 scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Fuji, K. Chem. Rev. 1993, 93, 2037-2066.
    • (1993) Chem. Rev , vol.93 , pp. 2037-2066
    • Fuji, K.1
  • 39
    • 0025762435 scopus 로고    scopus 로고
    • This auxiliary is used for a diastereoselective 1,4-addition reaction, a Guingant, A. Tetrahedron: Asymmetry 1991, 2, 415-418
    • This auxiliary is used for a diastereoselective 1,4-addition reaction. (a) Guingant, A. Tetrahedron: Asymmetry 1991, 2, 415-418.
  • 42
    • 41549154954 scopus 로고    scopus 로고
    • Single crystal used for the X-ray structural analysis was analyzed by HPLC to provide the same retention time as the major enantiomer
    • Single crystal used for the X-ray structural analysis was analyzed by HPLC to provide the same retention time as the major enantiomer.
  • 43
    • 33845557646 scopus 로고    scopus 로고
    • (S)-1-Methoxypentan-2-amine was prepared by methylation of L-(+)-isoleucinol with NaH/MeI according to Meyers et al.'s procedure: Meyers, A. I.; Williams, D. R.; Erickson, G. W.; White, S.; Druelinger, M. J. J. Am. Chem. Soc. 1981, 103, 3081-3087.
    • (S)-1-Methoxypentan-2-amine was prepared by methylation of L-(+)-isoleucinol with NaH/MeI according to Meyers et al.'s procedure: Meyers, A. I.; Williams, D. R.; Erickson, G. W.; White, S.; Druelinger, M. J. J. Am. Chem. Soc. 1981, 103, 3081-3087.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.