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Volumn 46, Issue 4, 2007, Pages 572-575

Total synthesis of paliurine F

Author keywords

Alkaloids; Copper; Enamides; Macrocyclization; Total synthesis

Indexed keywords

AMINES; AROMATIZATION; COPPER; ETHERS; REACTION KINETICS; SYNTHESIS (CHEMICAL);

EID: 33846522460     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200602865     Document Type: Article
Times cited : (112)

References (49)
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    • For asymmetric syntheses of trans-3-hydroxyprolinol derivatives, see: a C. Herdeis, H. P. Hubmann, H. Lotter, Tetrahedron: Asymmetry 1994, 5, 119-128;
    • For asymmetric syntheses of trans-3-hydroxyprolinol derivatives, see: a) C. Herdeis, H. P. Hubmann, H. Lotter, Tetrahedron: Asymmetry 1994, 5, 119-128;
  • 36
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    • The relative stereochemistry of 11 was confirmed by NOE experiments on the oxazolidinone obtained after reaction of 11 with sodium hydride; see the Supporting Information for more details.
    • The relative stereochemistry of 11 was confirmed by NOE experiments on the oxazolidinone obtained after reaction of 11 with sodium hydride; see the Supporting Information for more details.
  • 38
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    • 3, acetone) sequence; see the Supporting Information for more details.
    • 3, acetone) sequence; see the Supporting Information for more details.
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    • For the use of intermolecular amidation reactions in total syntheses of complex molecules, see: a
    • For the use of intermolecular amidation reactions in total syntheses of complex molecules, see: a) R. Shen, C. T. Lin, J. A. Porco, Jr., J. Am. Chem. Soc. 2002, 124, 5650-5651;
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 5650-5651
    • Shen, R.1    Lin, C.T.2    Porco Jr., J.A.3
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    • For macrocyclization using an intramolecular amidation of an aryl bromide, see: a
    • For macrocyclization using an intramolecular amidation of an aryl bromide, see: a) G. Cuny, M. Bois-Choussy, J. Zhu, Angew. Chem. 2003, 115, 4922-4925;
    • (2003) Angew. Chem , vol.115 , pp. 4922-4925
    • Cuny, G.1    Bois-Choussy, M.2    Zhu, J.3
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    • Angew. Chem. Int. Ed. 2003, 42, 4774-4777;
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    • [9] The reason for this discrepancy is unclear at present, although it might be attributed to contamination by a small amount of impurity in the natural sample.
    • [9] The reason for this discrepancy is unclear at present, although it might be attributed to contamination by a small amount of impurity in the natural sample.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.