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Volumn 16, Issue 22, 2005, Pages 3762-3766

Application of the N-hydroxymethyl group to the stereoselective synthesis of (3S,4S)-3-aminodeoxystatine derivatives

Author keywords

[No Author keywords available]

Indexed keywords

ACETAMIDE DERIVATIVE; AMIDE; CARBAMIC ACID; ESTER; LEUCINE; METHYL GROUP; N TERT BUTYLOXYCARBONYLLEUCINE; NITROGEN; STATINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 27944509636     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2005.10.018     Document Type: Article
Times cited : (15)

References (26)
  • 2
    • 0003723604 scopus 로고
    • A.J. Barrett G. Salvesen Elsevier New York
    • For a review, see: D.H. Rich A.J. Barrett G. Salvesen Proteinase Inhibitors 1986 Elsevier New York 179
    • (1986) Proteinase Inhibitors , pp. 179
    • Rich, D.H.1
  • 7
    • 27944490266 scopus 로고    scopus 로고
    • Ph.D. Thesis, Seoul National University, August
    • (d) Yoo, D. Ph.D. Thesis, Seoul National University, August, 2004.
    • (2004)
    • Yoo, D.1
  • 13
    • 0023718222 scopus 로고
    • The 3-aminodeoxystatine derivatives: H.J. Schostarez J. Org. Chem. 53 1988 3628 3631
    • (1988) J. Org. Chem. , vol.53 , pp. 3628-3631
    • Schostarez, H.J.1
  • 19
    • 27944444374 scopus 로고    scopus 로고
    • note
    • 7 resulted in mostly the deacetoxymethylation as shown below.
  • 24
    • 27944469917 scopus 로고    scopus 로고
    • note
    • 1H NMR spectrum. The smaller coupling constant of 5.1 Hz was attributed to the trans-isomer, whereas the larger coupling constant of 7.7 Hz to the cis-isomer.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.