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Volumn 5, Issue 4, 2003, Pages 495-498

Catalytic asymmetric synthesis of both syn- and anti-3,5-dihydroxy esters: Application to 1,3-polyol/α-pyrone natural product synthesis

Author keywords

[No Author keywords available]

Indexed keywords

1,3 POLYOL; 2 PYRONE DERIVATIVE; AMIDE; ESTER DERIVATIVE; IMIDAZOLE DERIVATIVE; KETONE; KETONE DERIVATIVE; LANTHANIDE; LANTHANIDE BINOL; MACROLIDE; STRICTIFOLIONE; UNCLASSIFIED DRUG; BIOLOGICAL FACTOR; ESTER; HYDROXYACID; PYRONE DERIVATIVE;

EID: 0038496699     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0273708     Document Type: Article
Times cited : (61)

References (32)
  • 6
    • 0033576439 scopus 로고    scopus 로고
    • For the one-pot, five-component linchpin coupling tactic, see: Smith, A. B., III; Pitram, S. M. Org. Lett. 1999, 1, 2001.
    • (1999) Org. Lett. , vol.1 , pp. 2001
    • Smith A.B. III1    Pitram, S.M.2
  • 7
    • 0030928918 scopus 로고    scopus 로고
    • Noyori hydrogenation: (a) Rychnovsky, S. D.; Khire, U. R.; Yang, G. J. Am. Chem. Soc. 1997, 119, 2058. (b) Sinz, C. J.; Rychnovsky, S. D. Angew. Chem., Int. Ed. 2001, 40, 3224.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 2058
    • Rychnovsky, S.D.1    Khire, U.R.2    Yang, G.3
  • 8
    • 0035801646 scopus 로고    scopus 로고
    • Noyori hydrogenation: (a) Rychnovsky, S. D.; Khire, U. R.; Yang, G. J. Am. Chem. Soc. 1997, 119, 2058. (b) Sinz, C. J.; Rychnovsky, S. D. Angew. Chem., Int. Ed. 2001, 40, 3224.
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 3224
    • Sinz, C.J.1    Rychnovsky, S.D.2
  • 11
    • 0000417893 scopus 로고    scopus 로고
    • Sharpless asymmetric dihydroxylation: (a) Hunter, T. J.; O'Doherty, G. A. Org. Lett. 2001, 3, 1049. (b) Hunter, T. J.; O'Doherty, G. A. Org. Lett. 2001, 3, 2777.
    • (2001) Org. Lett. , vol.3 , pp. 1049
    • Hunter, T.J.1    O'Doherty, G.A.2
  • 12
    • 0035940146 scopus 로고    scopus 로고
    • Sharpless asymmetric dihydroxylation: (a) Hunter, T. J.; O'Doherty, G. A. Org. Lett. 2001, 3, 1049. (b) Hunter, T. J.; O'Doherty, G. A. Org. Lett. 2001, 3, 2777.
    • (2001) Org. Lett. , vol.3 , pp. 2777
    • Hunter, T.J.1    O'Doherty, G.A.2
  • 18
    • 0141661666 scopus 로고    scopus 로고
    • note
    • For detailed data, see the Supporting Information.
  • 25
    • 0141438754 scopus 로고    scopus 로고
    • note
    • Enantiomeric excesses were determined by HPLC analysis.
  • 27
    • 0141550285 scopus 로고    scopus 로고
    • note
    • The absolute configuration was determined by Mosher's method after conversion to the corresponding β-hydroxy methyl ester.
  • 30
    • 0001399412 scopus 로고    scopus 로고
    • For representative reviews on ring-closing methathesis, see: (a) Ffirstner, A. Angew. Chem., Int. Ed. 2000, 39, 3012. (b) Grubbs, R. H.; Chang, S. Tetrahedron 1998, 54, 4413.
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 3012
    • Fürstner, A.1
  • 31
    • 0032580376 scopus 로고    scopus 로고
    • For representative reviews on ring-closing methathesis, see: (a) Ffirstner, A. Angew. Chem., Int. Ed. 2000, 39, 3012. (b) Grubbs, R. H.; Chang, S. Tetrahedron 1998, 54, 4413.
    • (1998) Tetrahedron , vol.54 , pp. 4413
    • Grubbs, R.H.1    Chang, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.