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Volumn 113, Issue 2, 1991, Pages 726-728

Bis(oxazolines) as Chiral Ligands in Metal-Catalyzed Asymmetric Reactions. Catalytic, Asymmetric Cyclopropanation of Olefins

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EID: 85008090337     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00002a080     Document Type: Article
Times cited : (1062)

References (23)
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    • and references cited therein.
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    • Scheffold, R., Ed.; Springer: Berlin
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    • (1989) Modern Synthetic Methods , vol.5 , pp. 199-248
    • Pfaltz, A.1
  • 6
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    • For previous uses of oxazoline-derived ligands, see: (a) Brunner, H.; Obermann, U. Chem. Ber. 1989, 122, 499–507.
    • (1989) Chem. Ber. , vol.122 , pp. 499-507
    • Brunner, H.1    Obermann, U.2
  • 10
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    • With chiral diazoacetate esters, Pfaltz has obtained an 82:18 trans/cis mixture in up to 97% ee for trans, 95% ee for cis.
    • Fritschi, H.; Leutenegger, U.; Pfaltz, A. Helv. Chim. Acta 1988, 71, 1553–1565. With chiral diazoacetate esters, Pfaltz has obtained an 82:18 trans/cis mixture in up to 97% ee for trans, 95% ee for cis.
    • (1988) Helv. Chim. Acta , vol.71 , pp. 1553-1565
    • Fritschi, H.1    Leutenegger, U.2    Pfaltz, A.3
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    • 2-symmetric ligands, see: Whitesell, J. K. Chem. Rev. 1989, 59, 1581–1590.
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    • Whitesell, J.K.1
  • 13
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    • 3). The assignment of absolute stereochemistry was made by comparison with literature values: (a) Inoue, Y.; Sugita, T.; Walborsky, H. M. Tetrahedron 1964, 20, 1695–1699.
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    • Inoue, Y.1    Sugita, T.2    Walborsky, H.M.3
  • 20
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    • When the Aratani catalyst was used, the product was isolated in 92% ee.
    • Aratani, T. Pure Appl. Chem. 1985, 57, 1839–1844. When the Aratani catalyst was used, the product was isolated in 92% ee.
    • (1985) Pure Appl. Chem. , vol.57 , pp. 1839-1844
    • Aratani, T.1
  • 21
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    • Doyle, M.P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.