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Volumn 107, Issue 12, 2007, Pages 5759-5812

Asymmetric catalysis mediated by synthetic peptides

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSTS; ENANTIOSELECTIVITY; PEPTIDES; PROTONATION;

EID: 38349112828     PISSN: 00092665     EISSN: None     Source Type: Journal    
DOI: 10.1021/cr068377w     Document Type: Review
Times cited : (556)

References (296)
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  • 26
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    • For recent reviews of proline catalyzed reactions, see: a
    • For recent reviews of proline catalyzed reactions, see: (a) List, B. Tetrahedron 2002, 58, 5573.
    • (2002) Tetrahedron , vol.58 , pp. 5573
    • List, B.1
  • 27
  • 34
    • 0037012379 scopus 로고    scopus 로고
    • For examples of micelles accelerating aldol reactions, see: (a) Dickerson, T. J, Janda, K. D. J. Am. Chem. Soc. 2002, 124, 3220
    • For examples of micelles accelerating aldol reactions, see: (a) Dickerson, T. J.; Janda, K. D. J. Am. Chem. Soc. 2002, 124, 3220.
  • 86
    • 33644594477 scopus 로고    scopus 로고
    • The Julia-Colorma epoxidation has been featured in several previous reviews: (a) Kelly, D. R.; Roberts, S. M. Biopolymers (Pept. Sci.) 2006, 84, 74.
    • The Julia-Colorma epoxidation has been featured in several previous reviews: (a) Kelly, D. R.; Roberts, S. M. Biopolymers (Pept. Sci.) 2006, 84, 74.
  • 108
    • 38349111214 scopus 로고    scopus 로고
    • A similar compilation appears in references 77a and 77d
    • A similar compilation appears in references 77a and 77d.
  • 141
    • 33847802878 scopus 로고    scopus 로고
    • Early work on enantioselective electrochemical reduction using (amino acid)-coated electrodes was carried out by Miller. See: Watkins, B. F.; Behling, J. R.; Kariv, E.; Miller, L. L. J. Am. Chem. Soc. 1975, 97, 3549.
    • Early work on enantioselective electrochemical reduction using (amino acid)-coated electrodes was carried out by Miller. See: Watkins, B. F.; Behling, J. R.; Kariv, E.; Miller, L. L. J. Am. Chem. Soc. 1975, 97, 3549.
  • 154
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    • Enantiomeric excess of product 74 was determined with chiral shift reagents: Ueyanagi, K.; Inoue, S. Makromol. Chem. 1977, 178, 235.
    • Enantiomeric excess of product 74 was determined with chiral shift reagents: Ueyanagi, K.; Inoue, S. Makromol. Chem. 1977, 178, 235.
  • 161
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    • See ref 62
    • See ref 62.
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    • For the use of amino acid-functionalized surfactants, see: b
    • For the use of amino acid-functionalized surfactants, see: (b) Brown, J. M.; Bunton, C. A. J. Chem. Soc., Chem. Commun. 1974, 969.
    • (1974) J. Chem. Soc., Chem. Commun , pp. 969
    • Brown, J.M.1    Bunton, C.A.2
  • 167
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    • For the use of N-protected amino acid derivatives and surfactants, see: f
    • For the use of N-protected amino acid derivatives and surfactants, see: (f) Inoue, T.; Nomura, K.; Kimizuka, H. Bull. Chem. Soc. Jpn. 1976, 49, 719.
    • (1976) Bull. Chem. Soc. Jpn , vol.49 , pp. 719
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    • See ref 59
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    • See ref 60
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    • See ref 61
    • See ref 61.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.