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Volumn 64, Issue 40, 2008, Pages 9592-9598

Synthesis of 1,3-bridged β-lactams embedded in a macrocyclic structure

Author keywords

[No Author keywords available]

Indexed keywords

1 [2 [(BUT 3 ENOYLOXY)METHYL]PHENYL) 4 (4 METHOXYPHENYL) 3 (PENT 4 ENAMIDO)AZETIDIN 2 ONE; 1 [2 [(BUT 3 ENOYLOXY)METHYL]PHENYL] 4 (4 METHOXYPHENYL) 3 (PENT 4 ENOYLOXY)AZETIDIN 2 ONE; 1 [2 [(PENT 4 ENOYLOXY)METHYL]PHENYL] 4 (4 METHOXYPHENYL) 3 (PENT 4 ENOYLOXY)AZETIDIN 2 ONE; 1 [2 [(TERT BUTYLDIMETHYLSILYLOXY)METHYL] PHENYL] 4 (4 METHOXYPHENYL) 3 (N PHTHALIMIDYL)AZETIDIN 2 ON; 3 (BUT 3 ENAMIDO) 1 [2 [(BUT 3 ENOYLOXY) METHYL]PHENYL] 4 (4 METHOXYPHENYL)AZETIDIN 2 ONE; 3 ACETOXY 1 [2 [(TERT BUTYLDIMETHYLSILYLOXY) METHYL]PHENYL) 4 (4 METHOXYPHENYL)AZETIDIN 2 ONE; 4 (4 METHOXYPHENYL) 3 (PENT 4 ENAMIDO) 1 [2 [(PENT 4 ENOYL OXY)METHYL]PHENYL]AZETIDIN 2 ONE; 4 (4 METHOXYPHENYL) 3 (PENT 4 ENAMIDO) 1 [2 [(PROP 2 ENOYLOXY)METHYL]PHENYL)AZETIDIN 2 ONE; BETA LACTAM DERIVATIVE; MACROCYCLIC LACTAM;

EID: 49349101883     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.07.046     Document Type: Article
Times cited : (9)

References (32)
  • 1
    • 0004030277 scopus 로고
    • Morin R.B., and Gorman M. (Eds), Academic, New York, NY
    • In: Morin R.B., and Gorman M. (Eds). Chemistry and Biology of β-Lactam Antibiotics Vols. 1-3 (1982), Academic, New York, NY
    • (1982) Chemistry and Biology of β-Lactam Antibiotics , vol.1-3
  • 2
    • 33746001269 scopus 로고    scopus 로고
    • The following review contains an excellent discussion in antibacterial natural products, resistance and future trends in antibacterial drugs:
    • The following review contains an excellent discussion in antibacterial natural products, resistance and future trends in antibacterial drugs:. von Nussbaum F., Brands M., Hinzen B., Weigand S., and Habich D. Angew. Chem., Int. Ed. 45 (2006) 5072
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 5072
    • von Nussbaum, F.1    Brands, M.2    Hinzen, B.3    Weigand, S.4    Habich, D.5
  • 4
    • 49349099286 scopus 로고    scopus 로고
    • Only a few examples of the synthesis of these elusive compounds have been reported to date, see
    • Only a few examples of the synthesis of these elusive compounds have been reported to date, see
  • 8
    • 49349112357 scopus 로고    scopus 로고
    • Few examples of macrocyclic β-lactams have been described to date. See:
    • Few examples of macrocyclic β-lactams have been described to date. See:
  • 12
    • 49349091375 scopus 로고    scopus 로고
    • Selected reviews on the applications of olefin metathesis, see:
    • Selected reviews on the applications of olefin metathesis, see:
  • 22
    • 49349108953 scopus 로고    scopus 로고
    • note
    • 3,4 coupling in the β-lactamic protons (J=1.9 Hz).
  • 23
    • 49349116307 scopus 로고    scopus 로고
    • note
    • Benzylidene-bis(tricyclohexylphosphine)dichlororuthenium. Aldrich 579726.
  • 24
    • 49349115474 scopus 로고    scopus 로고
    • note
    • (1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(phenylmethylene)(tricyclohexylphosphine)ruthenium. Aldrich 569747.
  • 31
    • 49349107279 scopus 로고    scopus 로고
    • note
    • 2 was fractionally distilled with benzene and the obtained acid chloride was used without further purification.
  • 32
    • 10044231720 scopus 로고    scopus 로고
    • 80% yield was assumed for the formation of this acid chloride
    • Ahrendt K.A., and Williams R.M. Org. Lett. 6 (2004) 4539 80% yield was assumed for the formation of this acid chloride
    • (2004) Org. Lett. , vol.6 , pp. 4539
    • Ahrendt, K.A.1    Williams, R.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.