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Volumn 40, Issue 20, 1999, Pages 3913-3916

A convergent, stereocontrolled synthesis of C2-symmetrical and pseudosymmetrical sulfur-tethered bis(amino alcohols)

Author keywords

Amino alcohols; Asymmetric synthesis; Enzyme inhibitor; Sulfides

Indexed keywords

AMINOALCOHOL; PROTEINASE INHIBITOR;

EID: 0033553384     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)00568-7     Document Type: Article
Times cited : (13)

References (31)
  • 21
    • 0025985752 scopus 로고
    • 10. These compounds are obtained in high enantiomeric purity by asymmetric epoxidation of (E)-allyl alcohols, followed by the regio- and stereoselective ring opening (by primary amines or by other nitrogen nucleophiles) of the resulting epoxy alcohols: Canas, M.; Poch, M.; Verdaguer, X.; Moyano, A.; Pericàs, M. A.; Riera, A. Tetrahedron Lett. 1991, 32, 6931-6934.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 6931-6934
    • Canas, M.1    Poch, M.2    Verdaguer, X.3    Moyano, A.4    Pericàs, M.A.5    Riera, A.6
  • 31
    • 0013554892 scopus 로고    scopus 로고
    • note
    • 2), 49.5 (CH), 50.1 (CH), 73.6 (2CH), 79.7 (2Cq), 155.8 (Cq), 156.1 (Cq).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.