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Volumn 6, Issue 20, 2004, Pages 3605-3607

Catalytic asymmetric synthesis of vicinal diamine derivatives through enantioselective N-allylation using chiral π-allyl Pd-catalyst

Author keywords

[No Author keywords available]

Indexed keywords

DIAMINE DERIVATIVE; OPIATE AGONIST; PALLADIUM; SIGMA OPIATE RECEPTOR;

EID: 6444242312     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol048498n     Document Type: Article
Times cited : (35)

References (33)
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    • For reviews on catalytic asymmetric allylation with a chiral π-allylpalladium complex, see: (a) Hayashi, T. In Catalytic Asymmetric Synthesis; Ojima, I., Ed.; VCH Publishers: New York, 1994; pp 325-365. (b) Trost, B. M.; Van Vranken, D. L. Chem. Rev. 1996, 96, 395. (c) Williams, J. M. Synlett, 1996, 705.
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    • For reviews on catalytic asymmetric allylation with a chiral π-allylpalladium complex, see: (a) Hayashi, T. In Catalytic Asymmetric Synthesis; Ojima, I., Ed.; VCH Publishers: New York, 1994; pp 325-365. (b) Trost, B. M.; Van Vranken, D. L. Chem. Rev. 1996, 96, 395. (c) Williams, J. M. Synlett, 1996, 705.
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    • For reviews on catalytic asymmetric allylation with a chiral π-allylpalladium complex, see: (a) Hayashi, T. In Catalytic Asymmetric Synthesis; Ojima, I., Ed.; VCH Publishers: New York, 1994; pp 325-365. (b) Trost, B. M.; Van Vranken, D. L. Chem. Rev. 1996, 96, 395. (c) Williams, J. M. Synlett, 1996, 705.
    • (1996) Synlett , pp. 705
    • Williams, J.M.1
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    • note
    • The reverse of the enantioselectivity in the reaction of 1e was confirmed by converting 2e to 2a (see the Supporting Information). The absolute configuration of the major enantiomer of the product 2d was also determined by conversion to 2a (see the Supporting Information), while that of 2c was not determined.
  • 24
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    • note
    • The absolute configuration of the product 2f was not determined.
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    • Trost, B.M.1    Kruger, A.C.2    Bunt, R.C.3    Zambrano, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.