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Volumn 12, Issue 22, 2010, Pages 5274-5277

Enantioselective synthesis of anti -β-hydroxy-α-amido esters via transfer hydrogenation

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; ESTER;

EID: 78449267573     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol102323k     Document Type: Article
Times cited : (64)

References (61)
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    • Homogeneous Hydrogenations. in
    • For recent reviews on hydrogenation and transfer hydrogenation, see:;,;, Eds.; Wiley-VCH Verlag GmbH & Co KGaA: Weinheim
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    • Ohkuma, T.1    Noyori, R.2    Beller, M.3    Bolm, C.4
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    • For reviews on DKR, see:; Angew. Chem., Int. Ed. 2005, 44, 3974-4001
    • Noyori, R.; Ohkuma, T. Angew. Chem., Int. Ed. 2001, 40, 40-73 For reviews on DKR, see: Vedejs, E.; Jure, M. Angew. Chem., Int. Ed. 2005, 44, 3974-4001
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 40-73
    • Noyori, R.1    Ohkuma, T.2    Vedejs, E.3    Jure, M.4
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    • Synthesis of syn -β-hydroxy-α-amino esters
    • Synthesis of syn -β-hydroxy-α-amino esters
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    • Synthesis of Amino Acid Derivatives via Asymmetric Hydrogenation. in
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    • Shimizu, H.; Nagasaki, I.; Sayo, N.; Saito, T. Synthesis of Amino Acid Derivatives via Asymmetric Hydrogenation. In Asymmetric Synthesis and Application of α-Amino Acids; American Chemical Society: Washington, D.C., 2009; Vol. 1009, pp 203 - 226.
    • (2009) Asymmetric Synthesis and Application of α-Amino Acids , pp. 203-226
    • Shimizu, H.1    Nagasaki, I.2    Sayo, N.3    Saito, T.4
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    • Synthesis of anti -β-hydroxy-α-amino esters
    • Synthesis of anti -β-hydroxy-α-amino esters
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    • Stereoselective Synthesis of anti -β-Hydroxy-α-Amino Acids Using anti -Selective Asymmetric Hydrogenation. in
    • American Chemical Society: Washington, D.C. 1009
    • Hamada, Y.; Makino, K. Stereoselective Synthesis of anti -β-Hydroxy-α-Amino Acids Using anti -Selective Asymmetric Hydrogenation. In Asymmetric Synthesis and Application of α-Amino Acids; American Chemical Society: Washington, D.C., 2009; Vol. 1009, pp 227 - 238.
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    • The exception being developments discussed in ref 9c
    • The exception being developments discussed in ref 9c.
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    • Synthesis of syn -β-hydroxy-α-amino esters using transfer hydrogenation
    • Synthesis of syn -β-hydroxy-α-amino esters using transfer hydrogenation
  • 48
    • 78449309876 scopus 로고    scopus 로고
    • 1H NMR analysis of the relevant J coupling values. See
    • 1H NMR analysis of the relevant J coupling values. See
  • 52
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    • 3N (5:2) complex
    • 3N (5:2) complex.
  • 53
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    • Running the reaction for only two days and 20 mol % catalyst yielded the product in 55% yield and 96:4 er
    • Running the reaction for only two days and 20 mol % catalyst yielded the product in 55% yield and 96:4 er.
  • 54
    • 78449294055 scopus 로고    scopus 로고
    • Ortho-substituted aromatics are not reported in any of the references 9. However, ortho-substituted aromatic ketones have been reduced using ATH. For an example, see
    • Ortho-substituted aromatics are not reported in any of the references 9. However, ortho-substituted aromatic ketones have been reduced using ATH. For an example, see
  • 58
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    • The absolute stereochemistry has not been determined
    • The absolute stereochemistry has not been determined.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.