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Volumn 45, Issue 7, 2006, Pages 1126-1130

A biomimetic chromanol cyclization leading to α-tocopherol

Author keywords

Biomimetic synthesis; Cyclization; Diastereoselectivity; Enzyme catalysis; Peptides

Indexed keywords

BIOMIMETIC SYNTHESIS; CYCLIZATION; DIASTEREOSELECTIVITY; ENZYME CATALYSIS; PEPTIDES;

EID: 33746316224     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200503123     Document Type: Article
Times cited : (42)

References (14)
  • 14
    • 33746286957 scopus 로고    scopus 로고
    • unpublished results
    • The diastereo-face-selectivity depends on the configurations of the dipeptide, whereas the influence of the camphanoyl unit is negligible. The use of (-)-camphanate is purely for convenience, as tocopherols that are epimeric at C2 can be separated by HPLC and hence the de of the cyclization can be easily determined (C. Grütter, E. Alonso, A. Chougnet, W.-D. Woggon, unpublished results).
    • Grütter, C.1    Alonso, E.2    Chougnet, A.3    Woggon, W.-D.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.