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Volumn 8, Issue 20, 2010, Pages 4736-4743

Highly efficient and enantioselective biotransformations of β-lactam carbonitriles and carboxamides and their synthetic applications

Author keywords

[No Author keywords available]

Indexed keywords

ACID PRODUCTS; AMIDASE; CARBONITRILES; CARBOXAMIDES; ENANTIOPURE; ENANTIOSELECTIVE; FACILE PREPARATION; FUNCTIONALIZED; HETEROCYCLIC COMPOUND; NITRILE HYDRATASES; RHODOCOCCUS ERYTHROPOLIS; SYNTHETIC APPLICATION; WHOLE CELL;

EID: 77957665802     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c0ob00198h     Document Type: Article
Times cited : (17)

References (45)
  • 1
    • 0004030277 scopus 로고
    • R. B. Morin and M. Gorman, Academic Press, New York
    • Chemistry and Biology of β-Lactam Antibiotics, ed., R. B. Morin, and, M. Gorman,, Academic Press, New York, 1982, vol. 1-3
    • (1982) Chemistry and Biology of β-Lactam Antibiotics , vol.1-3
  • 8
    • 0345016367 scopus 로고    scopus 로고
    • Very recently, a sequential Candida antarctica lipase B-catalyzed deacylation and lactam ring-opening of racemic cis-3-acetoxyl-4-phenylazetidin- 2-one was reported to produce enantiopure β-lactam and 3-phenylisoserine.
    • R. N. Patel J. Howell R. Chidambaram S. Benoit J. Kant Tetrahedron: Asymmetry 2003 14 3673
    • (2003) Tetrahedron: Asymmetry , vol.14 , pp. 3673
    • Patel, R.N.1    Howell, J.2    Chidambaram, R.3    Benoit, S.4    Kant, J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.