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Volumn 32, Issue 2, 2003, Pages 190-191

The new and efficient synthesis of a heptose moiety of spicamycin

Author keywords

[No Author keywords available]

Indexed keywords

7 O ACETYL 4 AZIDO 2,3,6 TRI O BENZYL 4 DEOXYGLYCERO ALPHA MANNOHEPTOPYRANOSYLACETATE; ACETIC ACID DERIVATIVE; ANTIBIOTIC AGENT; ANTINEOPLASTIC AGENT; HEPTOSE; RIBOSE; SPICAMYCIN; UNCLASSIFIED DRUG;

EID: 0038221138     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.2003.190     Document Type: Article
Times cited : (14)

References (22)
  • 17
    • 0038304633 scopus 로고    scopus 로고
    • note
    • 13C NMR, IR, and mass spectrometric and/or elemental analyses.
  • 18
    • 0038304634 scopus 로고    scopus 로고
    • note
    • When this reaction was carried out in MeOH (CSA, 100°C, in a sealed tube for 60 h), the desired methyl α-pyranoside was obtained as the minor product (33% yield), and the starting methyl furanoside 9 was recovered in 57% yield.
  • 19
    • 0037629130 scopus 로고    scopus 로고
    • note
    • iPrOH, 120°C) of β-furanoside gave additional 13 in 50% yield (28% recovery of the starting β-furanoside).
  • 22
    • 0037629129 scopus 로고    scopus 로고
    • note
    • +): 589.2424, Found: m/z 589.2436.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.