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Volumn 18, Issue 2, 2007, Pages 208-214

Synthesis of optically active cyanohydrins from aromatic ketones: evidence of an increased substrate range and inverted stereoselectivity for the hydroxynitrile lyase from Linum usitatissimum

Author keywords

[No Author keywords available]

Indexed keywords

ACETONE; AROMATIC COMPOUND; BENZYLACETONE; CARBON; CYANIDE; CYANOHYDRIN; HYDROXYNITRILE LYASE; KETONE DERIVATIVE; PHENYLACETONE; PROPIOPHENONE; UNCLASSIFIED DRUG;

EID: 33847174501     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2006.12.026     Document Type: Article
Times cited : (29)

References (27)
  • 16
    • 33847139901 scopus 로고    scopus 로고
    • note
    • 11 The pH of the buffer component of the reaction mixture was set at 4.5, chosen to balance the requirements for minimizing both enzyme instability that is known to be more pronounced at pH < 5 (see Albrecht, J.; Jansen, I.; Kula, M.-R. Biotechnol. Appl. Biochem. 1993, 17, 191), and the rate of non-enzymatic spontaneous cyanide addition that is increased at pH > 4 and leads to racemic product formation (see Kragl, U.; Niedermeyer, U.; Kula, M.-R.; Wandrey, C. Ann. NY Acad. Sci. 1990, 613, 617).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.