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Volumn 39, Issue 18, 1998, Pages 2823-2826

Enantioselectivity and diastereoselectivity in the hydrolysis of acylals and structurally related esters of secondary alcohols with Candida rugosa lipase

Author keywords

[No Author keywords available]

Indexed keywords

ACYLAL; ESTER DERIVATIVE; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG;

EID: 0032580468     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00256-1     Document Type: Article
Times cited : (18)

References (20)
  • 5
    • 0024382916 scopus 로고
    • e) Wong, C. -H. Science 1989, 244, 1145.
    • (1989) Science , vol.244 , pp. 1145
    • Wong, C.-H.1
  • 10
    • 0010725518 scopus 로고    scopus 로고
    • note
    • 5. α-selectivity refers to the carbon which bears the oxygen substituent, and β-selectivity refers to the carbon next to the α-carbon.
  • 11
    • 0242528545 scopus 로고
    • 6. a) For the effect of the size of substituents in β position of primary alcohols see: Weissfloch, A. N. E.; Kazlauskas, R. J. J. Org. Chem. 1995, 60, 6959-6969.
    • (1995) J. Org. Chem. , vol.60 , pp. 6959-6969
    • Weissfloch, A.N.E.1    Kazlauskas, R.J.2
  • 12
    • 0010640776 scopus 로고    scopus 로고
    • note
    • b) For the effect of the size of substituents in β position for secondary alcohols see also reference 12.
  • 16
    • 33947085552 scopus 로고
    • 10. Assumed by correlation of downfield and upfield 1H NMR signals according to Dale, J. A.; Mosher H. S. J. Am. Chem. Soc. 1973, 95, 512.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 512
    • Dale, J.A.1    Mosher, H.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.