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Volumn 68, Issue 37, 2012, Pages 7670-7674

Chemoenzymatic preparation of optically active trans- and cis-cyclohex-4-ene-1,2-diamine and trans-6-aminocyclohex-3-enol derivatives

Author keywords

Aminolysis; Lipase; Transesterification; Vicinal amino alcohols; Vicinal diamines

Indexed keywords

AMINOALCOHOL; CYCLOHEXENE DERIVATIVE; DIAMINE DERIVATIVE; OSELTAMIVIR; TRIACYLGLYCEROL LIPASE;

EID: 84864474102     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.05.087     Document Type: Conference Paper
Times cited : (5)

References (30)
  • 2
    • 70349095283 scopus 로고    scopus 로고
    • For a review, see: J. Magano Chem. Rev. 109 2009 4398 4438
    • (2009) Chem. Rev. , vol.109 , pp. 4398-4438
    • Magano, J.1
  • 20
    • 84864450699 scopus 로고    scopus 로고
    • Program 'Selectivity'
    • Program 'Selectivity' http://borgc185.kfunigraz.ac.at/sites/research/ model.htm.
  • 21
  • 26
    • 84890232906 scopus 로고    scopus 로고
    • Thus far, lipase from Burkholderia cepacia (before classified as Pseudomonas cepacia) has proven to be the most effective catalyst for the resolution of secondary alcohols. See for example: 2nd ed. Wiley-VCH Weinheim Chapter 5
    • Thus far, lipase from Burkholderia cepacia (before classified as Pseudomonas cepacia) has proven to be the most effective catalyst for the resolution of secondary alcohols. See for example: U.T. Bornscheuer, and R.J. Kazlauskas Hydrolases in Organic Synthesis Regio- and Stereoselective Biotransformations 2nd ed. 2006 Wiley-VCH Weinheim Chapter 5
    • (2006) Hydrolases in Organic Synthesis Regio- And Stereoselective Biotransformations
    • Bornscheuer, U.T.1    Kazlauskas, R.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.