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Volumn 10, Issue 12, 2007, Pages 1180-1186

Enantiopure aryl-[1,2,5,6-tetrahydro-pyridinyl] methanols and their use for heterogeneous hydrogenation of ethyl pyruvate

Author keywords

Anthryl 1,2,5,6 tetrahydro pyridyl methanol; Asymmetric heterogeneous hydrogenation; Chiral modifiers; Enantiopure aryl tetrahydro methanols; Naphtyl 1,2,5,6 tetrahydro pyridyl methanol

Indexed keywords


EID: 36749050858     PISSN: 16310748     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.crci.2007.06.003     Document Type: Article
Times cited : (4)

References (22)
  • 3
    • 17544378316 scopus 로고    scopus 로고
    • and included references for previous reviews
    • Bürgi T., and Baiker A. Acc. Chem. Res. 37 (2004) 909 and included references for previous reviews
    • (2004) Acc. Chem. Res. , vol.37 , pp. 909
    • Bürgi, T.1    Baiker, A.2
  • 4
    • 17544373640 scopus 로고    scopus 로고
    • and included references for previous reviews
    • Baiker A. Catal. Today 100 (2005) 159 and included references for previous reviews
    • (2005) Catal. Today , vol.100 , pp. 159
    • Baiker, A.1
  • 5
    • 36749068979 scopus 로고    scopus 로고
    • C. Marsol, Ph.D., Strasbourg University, France, 2001 (started 1998);
  • 6
    • 36749050374 scopus 로고    scopus 로고
    • A. Solladié-Cavallo, C. Marsol, F. Garin, Second European Catalysis Symposium, Pisa, Italy, 2001;
  • 8
    • 36749091167 scopus 로고    scopus 로고
    • K. Azyat, Ph.D., Strasbourg University, France, 2005 (started 2002).
  • 11
    • 36749052320 scopus 로고    scopus 로고
    • For comparison of anthryl and naphthyl groups cf.;
  • 18
    • 0037185570 scopus 로고    scopus 로고
    • For the preparation of six-membered ring through ring-closing metathesis using Grubbs catalyst see:
    • For the preparation of six-membered ring through ring-closing metathesis using Grubbs catalyst see:. Ginesta X., Pericàs M.A., and Riera A. Tetrahedron Lett. (2002) 779
    • (2002) Tetrahedron Lett. , pp. 779
    • Ginesta, X.1    Pericàs, M.A.2    Riera, A.3
  • 19
    • 0000966495 scopus 로고    scopus 로고
    • Ethyl lactate having an enantiomeric excess up to 95% can be obtained with CD according to adjustment of the reactions conditions ( ) one may thus expect that higher e.e.% could also be obtained with 1 and 4H by optimizing the reaction conditions
    • Ethyl lactate having an enantiomeric excess up to 95% can be obtained with CD according to adjustment of the reactions conditions (. Blaser H.U., Jalett H.P., Müller M., and Studer M. Catal. Today 37 (1997) 441 ) one may thus expect that higher e.e.% could also be obtained with 1 and 4H by optimizing the reaction conditions
    • (1997) Catal. Today , vol.37 , pp. 441
    • Blaser, H.U.1    Jalett, H.P.2    Müller, M.3    Studer, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.