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Volumn 55, Issue 3, 1999, Pages 687-698

Synthetic studies of moenomycin a disaccharide analogues. Protection of the anomeric centre with long-chain protective groups

Author keywords

Antibiotics; Carbohydrates; Protecting groups

Indexed keywords

ALLYL COMPOUND; CARBOHYDRATE; DISACCHARIDE; GLUCOPYRANOSIDE; MOENOMYCIN A;

EID: 0033555377     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(98)01062-X     Document Type: Article
Times cited : (11)

References (29)
  • 5
    • 85038197350 scopus 로고
    • Dissertation, Bochum
    • Heuer, M. Dissertation, Bochum 1993.
    • (1993)
    • Heuer, M.1
  • 10
    • 85038197031 scopus 로고    scopus 로고
    • The concentration was about 0.2 M.
    • The concentration was about 0.2 M.
  • 17
    • 85038206312 scopus 로고    scopus 로고
    • 13
    • 13
  • 24
    • 85038193733 scopus 로고    scopus 로고
    • Dissertation, Leipzig
    • Attempts to perform the oxidation with a free -OH group or a -O-acetyl protecting group met with no success. Rather than yielding the desired compound an elimination reaction took place leading to hex-4-ene-pyranoside derivatives: Weigelt, D., Dissertation, Leipzig 1996.
    • (1996)
    • Weigelt, D.1
  • 25
    • 85038197746 scopus 로고    scopus 로고
    • Diploma Thesis, Leipzig
    • Brüschke, K., Diploma Thesis, Leipzig 1997.
    • (1997)
    • Brüschke, K.1
  • 26
    • 85038201305 scopus 로고    scopus 로고
    • note
    • In the case of diol 11a some methanol had to be added.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.