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Volumn 17, Issue 14, 2006, Pages 2154-2182

Solvent and in situ catalyst preparation impacts upon Noyori reductions of aryl-chloromethyl ketones: application to syntheses of chiral 2-amino-1-aryl-ethanols

Author keywords

[No Author keywords available]

Indexed keywords

2 CHLOROETHANOL; 2 METHYLAMINOETHANOL; ALCOHOL DERIVATIVE; KETONE DERIVATIVE; SOLVENT;

EID: 33748203034     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2006.07.017     Document Type: Article
Times cited : (50)

References (63)
  • 10
    • 33748199195 scopus 로고    scopus 로고
    • Ar = 3-pyridyl: Smith, R.G. WO971689 A1 19970509.
  • 11
    • 33748181562 scopus 로고    scopus 로고
    • Ar = 3-pyridyl: Fisher, M. H.; Naylor, E. M.; Ok, D.; Webber, A. E.; Shih, T.; Ok, H. US 5561142, 1996.
  • 23
    • 0031550862 scopus 로고    scopus 로고
    • For other oxazaborolidine reductions applied to aryl halomethyl ketones (not heteroaryl) see:
    • For other oxazaborolidine reductions applied to aryl halomethyl ketones (not heteroaryl) see:. Salunkhe A.M., and Burkhardt E.R. Tetrahedron Lett. 38 (1997) 1523-1526
    • (1997) Tetrahedron Lett. , vol.38 , pp. 1523-1526
    • Salunkhe, A.M.1    Burkhardt, E.R.2
  • 30
    • 0002123299 scopus 로고    scopus 로고
    • and references cited therein
    • Noyori R., and Hashiguchi S. Acc. Chem. Res. 30 (1997) 97-102 and references cited therein
    • (1997) Acc. Chem. Res. , vol.30 , pp. 97-102
    • Noyori, R.1    Hashiguchi, S.2
  • 32
    • 5444236447 scopus 로고    scopus 로고
    • For some recent reports of advances in Noyori-type reductions of somewhat related ketones see:
    • For some recent reports of advances in Noyori-type reductions of somewhat related ketones see:. Hamada T., Torii T., Onishi T., Izawa K., and Ikariya T. J. Org. Chem. 69 (2004) 7391-7394
    • (2004) J. Org. Chem. , vol.69 , pp. 7391-7394
    • Hamada, T.1    Torii, T.2    Onishi, T.3    Izawa, K.4    Ikariya, T.5
  • 40
    • 0141854157 scopus 로고    scopus 로고
    • For recent Noyori-type reductions of relevant aryl halomethyl ketones (Eq. 1) see: Ar = Ph (Br):
    • For recent Noyori-type reductions of relevant aryl halomethyl ketones (Eq. 1) see: Ar = Ph (Br):. Ma Y., Liu H., Chen L., Cui X., Zhu J., and Deng J. Org. Lett. 5 (2003) 2103-2106
    • (2003) Org. Lett. , vol.5 , pp. 2103-2106
    • Ma, Y.1    Liu, H.2    Chen, L.3    Cui, X.4    Zhu, J.5    Deng, J.6
  • 41
    • 3342948477 scopus 로고    scopus 로고
    • Ar = phenyl, 3-pyridyl, 2-furyl, 2-thienyl (Cl):
    • Ar = phenyl, 3-pyridyl, 2-furyl, 2-thienyl (Cl):. Hamada T., Torii T., Izawa K., and Ikariya T. Tetrahedron 60 (2004) 7411-7417
    • (2004) Tetrahedron , vol.60 , pp. 7411-7417
    • Hamada, T.1    Torii, T.2    Izawa, K.3    Ikariya, T.4
  • 43
    • 33748150513 scopus 로고    scopus 로고
    • Ar = benzofuranyl (Br, Cl) see Ref. 2b.
  • 46
    • 33748190814 scopus 로고    scopus 로고
    • note
    • Chiracel OJ (5 cm × 50 cm), i-PrOH/heptane 10:90.
  • 59
    • 33748143440 scopus 로고    scopus 로고
    • Dolling, U. H.; Frey, L. F.; Tillyer, R. D.; Tschaen, D. M. WO 9710195 March 20, 1997.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.