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Volumn 61, Issue 43, 2005, Pages 10277-10284

Erratum: A general strategy for the synthesis of azapeptidomimetic lactams (Tetrahedron (2005) 61 (10277) DOI: 10.1016/j.tet.2005.08.029);A general strategy for the synthesis of azapeptidomimetic lactams

Author keywords

Azapeptide; Lactams; Mitsunobu reaction; Peptidomimetic

Indexed keywords

2 PYRROLIDINONE; ALANINE DERIVATIVE; AMINO ACID; BETA LACTAM; LACTAM DERIVATIVE; SERINE;

EID: 25144488663     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.11.025     Document Type: Erratum
Times cited : (24)

References (59)
  • 35
    • 0033591141 scopus 로고    scopus 로고
    • For reviews of β-lactone synthesis and reactions see: (a) H.W. Yang, and D. Romo Tetrahedron 55 1999 6403 6434
    • (1999) Tetrahedron , vol.55 , pp. 6403-6434
    • Yang, H.W.1    Romo, D.2
  • 54
    • 0020582691 scopus 로고
    • O-alkylation has been seen with the related Mitsunobu reaction of acyl hydroxamates in e-caprolactam synthesis, see for example: (a) P.J. Maurer, and M.J. Miller J. Am. Chem. Soc. 105 1983 240 245
    • (1983) J. Am. Chem. Soc. , vol.105 , pp. 240-245
    • Maurer, P.J.1    Miller, M.J.2
  • 55
    • 0019517569 scopus 로고
    • P.J. Maurer, and M.J. Miller J. Org. Chem. 46 1981 2835 2836 Nevertheless, we did not see any O-alkylation products based on a close analysis of NMR and IR (see supplementary materials)
    • (1981) J. Org. Chem. , vol.46 , pp. 2835-2836
    • Maurer, P.J.1    Miller, M.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.