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Volumn 137, Issue 2, 2015, Pages 999-1006

Catalytic, asymmetric, and stereodivergent synthesis of non-symmetric β,β-Diaryl-α-Amino Acids

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL REACTIONS; ENANTIOSELECTIVITY; HYDROGENATION; STEREOCHEMISTRY; STEREOSELECTIVITY; SULFUR COMPOUNDS;

EID: 84921452781     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja511872a     Document Type: Article
Times cited : (99)

References (85)
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    • 3 rd ed. Ojima, I. John Wiley & Sons: Hoboken, NJ, Chapter 7
    • Shang, G.; Li, W.; Zhang, Z. In Catalytic Asymmetric Synthesis, 3 rd ed.; Ojima, I., Ed.; John Wiley & Sons: Hoboken, NJ, 2010; Chapter 7, pp 343-436.
    • (2010) Catalytic Asymmetric Synthesis , pp. 343-436
    • Shang, G.1    Li, W.2    Zhang, Z.3
  • 46
    • 84904822853 scopus 로고    scopus 로고
    • Soloshonok, V. A. Izawa, K. ACS Symposium Series 1009; American Chemical Society: Washington, DC, Chapter 13
    • Shimizu, H.; Nagasaki, I.; Sayo, N.; Saito, T. In Asymmetric Synthesis and Application of α-Amino Acids; Soloshonok, V. A.; Izawa, K., Eds.; ACS Symposium Series 1009; American Chemical Society: Washington, DC, 2009; Chapter 13; 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
  • 71
    • 77956032927 scopus 로고    scopus 로고
    • Related scrambling in Suzuki-Miyaura coupling of β-ketoester derived enol tosylates has been reported. See
    • Related scrambling in Suzuki-Miyaura coupling of β-ketoester derived enol tosylates has been reported. See: Nishikado, H.; Nakatsuji, H.; Ueno, K.; Nagase, R.; Tanabe, Y. Synlett 2010, 2087-2092
    • (2010) Synlett , pp. 2087-2092
    • Nishikado, H.1    Nakatsuji, H.2    Ueno, K.3    Nagase, R.4    Tanabe, Y.5
  • 72
    • 38049047508 scopus 로고    scopus 로고
    • For a description of the microscale screening conditions utilized in this study see
    • For a description of the microscale screening conditions utilized in this study see: Shultz, C. S.; Krska, S. Acc. Chem. Res. 2007, 40, 1320-1326
    • (2007) Acc. Chem. Res. , vol.40 , pp. 1320-1326
    • Shultz, C.S.1    Krska, S.2
  • 81
    • 84921528418 scopus 로고    scopus 로고
    • For a previous report of attempted but unsuccessful reduction of a symmetric N -Boc-β,β-bis(4-fluorophenyl) dehydroaminoacid ester see reference 8p
    • For a previous report of attempted but unsuccessful reduction of a symmetric N -Boc-β,β-bis(4-fluorophenyl) dehydroaminoacid ester see reference 8p.
  • 82
    • 84921447749 scopus 로고    scopus 로고
    • Geometry optimizations were performed using Spartan10, version 1.1.0; Wavefunction, Inc. Irvine, CA, using the B3LYP density functional with 6-31G∗ basis sets
    • Geometry optimizations were performed using Spartan10, version 1.1.0; Wavefunction, Inc.: Irvine, CA, 2011, using the B3LYP density functional with 6-31G∗ basis sets.
    • (2011)
  • 85
    • 84921509264 scopus 로고    scopus 로고
    • Crystallographic information has been deposited with the Cambridge Crystallographic Database and is available online at. See CCDC deposition 1033704
    • Crystallographic information has been deposited with the Cambridge Crystallographic Database and is available online at http://www.ccdc.cam.ac.uk/Community/Requestastructure/Pages/DataRequest.aspx. See CCDC deposition 1033704.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.