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Volumn 67, Issue 34, 2011, Pages 6155-6165

Enantioselective epoxidation of α,β-unsaturated ketones catalyzed by stapled helical l-Leu-based peptides

Author keywords

, Unsaturated ketones; Enantioselective epoxidation; Helix; Organocatalyst; Stapled peptide

Indexed keywords

ALPHA CRYSTALLIN; EPOXIDE; HEPTAPEPTIDE; KETONE DERIVATIVE; LEUCINE;

EID: 79960573401     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.06.075     Document Type: Article
Times cited : (48)

References (54)
  • 34
    • 6344260329 scopus 로고    scopus 로고
    • It has already been known that (Z)-chalcone is isomerised under hydroperoxide conditions to an equimolar mixture of the (Z)- and (E)-isomers prior to epoxidation. See reference:, Therefore, the authors did not attempt to examine the epoxidation to (Z)-chalcone
    • It has already been known that (Z)-chalcone is isomerised under hydroperoxide conditions to an equimolar mixture of the (Z)- and (E)-isomers prior to epoxidation. See reference: D.R. Kelly, E. Caroff, R.W. Flood, W. Heal, and S.M. Roberts Chem. Commun. 2004 2016 2017 Therefore, the authors did not attempt to examine the epoxidation to (Z)-chalcone
    • (2004) Chem. Commun. , pp. 2016-2017
    • Kelly, D.R.1    Caroff, E.2    Flood, R.W.3    Heal, W.4    Roberts, S.M.5
  • 42
    • 79960607051 scopus 로고    scopus 로고
    • CCDC-797487 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge at (or from the Cambridge Crystallographic Data Center, 12, Union Road, Cambridge CB2 1EZ, UK; fax: (+44) 1223-336-033; or deposit@ccdc.cam.ac.uk).
    • CCDC-797487 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge at www.ccdc.cam.ac.uk/conts/ retrieving.html (or from the Cambridge Crystallographic Data Center, 12, Union Road, Cambridge CB2 1EZ, UK; fax: (+44) 1223-336-033; or deposit@ccdc.cam.ac.uk) .


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.