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Volumn 63, Issue 4, 1998, Pages 1221-1225

Asymmetric Total Synthesis of an Important 3-(Hydroxymethyl)carbacephalosporin

Author keywords

[No Author keywords available]

Indexed keywords

3 (HYDROXYMETHYL)CARBACEPHALOSPORIN; ANTIINFECTIVE AGENT; BETA LACTAM ANTIBIOTIC; CARBACEPHALOSPORIN; QUINOLONE; UNCLASSIFIED DRUG;

EID: 0032548869     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo971772p     Document Type: Article
Times cited : (27)

References (47)
  • 12
    • 0007861946 scopus 로고
    • Page, M. I., Ed.; Chapman & Hall: London
    • Cooper, R. D. G. In The Chemistry of β-Lactams; Page, M. I., Ed.; Chapman & Hall: London, 1992; pp 272-305.
    • (1992) The Chemistry of Β-Lactams , pp. 272-305
    • Cooper, R.D.G.1
  • 39
    • 85034467198 scopus 로고
    • Reston, VA, May 5-6
    • β-Hydroxy-α-amino acid 11 was a generous gift of Eli Lilly and Co. It was prepared at Lilly by large-scale serinehydroxymethyltransferase (SHMT)-mediated condensation of glycine and pentenal with subsequent protection of the α-amino group as a phthalimido group. Jackson, W. C. et. al., Chiral, Reston, VA, May 5-6, 1994.
    • (1994) Chiral
    • Jackson, W.C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.