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Volumn 3, Issue 17, 2001, Pages 2621-2624

Enantioselective synthesis of fluorinated α-amino acids and derivatives in combination with ring-closing metathesis: Intramolecular π-stacking interactions as a source of stereocontrol

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; FLUORINE;

EID: 18044400040     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol016087q     Document Type: Article
Times cited : (69)

References (26)
  • 3
    • 12044259820 scopus 로고
    • and literature cited therein
    • (c) Edge-to-face aromatic interactions have also been invoked in many examples of molecular recognition. See, for example: Paliwal, S.; Greib, S.; Wilcox, C. S. J. Am. Chem. Soc. 1994, 116, 4497-4498 and literature cited therein.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 4497-4498
    • Paliwal, S.1    Greib, S.2    Wilcox, C.S.3
  • 14
    • 0000632739 scopus 로고
    • π-Stacking between aromatic rings in protic solvents have been described in the literature: (a) Kool, E. T.; Breslow, R. K. J. Am. Chem. Soc. 1988, 110, 1596-1597.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 1596-1597
    • Kool, E.T.1    Breslow, R.K.2
  • 16
    • 0035825778 scopus 로고    scopus 로고
    • and references therein
    • An efficient catalytic asymmetric synthesis of α-amino acids has been very recently described, See: Abe, H.; Amii, H.; Uneyama, K. Org. Lett. 2001, 3, 313-315 and references therein.
    • (2001) Org. Lett. , vol.3 , pp. 313-315
    • Abe, H.1    Amii, H.2    Uneyama, K.3
  • 17
    • 0041295494 scopus 로고    scopus 로고
    • note
    • s)-5e will be published in a full account of this work.
  • 18
    • 0032580376 scopus 로고    scopus 로고
    • RCM has emerged as a prominent reaction for the synthesis of medium- and large-sized rings from acyclic diene precursors. See, for example: (a) Grubbs, R. H.; Chang, S. Tetrahedron 1998, 54, 4413-4450.
    • (1998) Tetrahedron , vol.54 , pp. 4413-4450
    • Grubbs, R.H.1    Chang, S.2
  • 21
    • 0001811974 scopus 로고    scopus 로고
    • RCM has been used to prepare a variety of nitrogen-containing natural products including peptidomimetics: Phillips, A. J.; Abell, A. D. Aldrichimica Acta 1999, 32, 75-89.
    • (1999) Aldrichimica Acta , vol.32 , pp. 75-89
    • Phillips, A.J.1    Abell, A.D.2
  • 26
    • 0041295493 scopus 로고    scopus 로고
    • note
    • 2) with NaH followed by N-alkylation of the previously isolated N-unsubstituted oxazolidinone.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.