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Volumn 10, Issue 16, 2008, Pages 3611-3614

Use of enantiomerically pure 7-azabicyclo[2.2.1]heptan-2-ol as a chiral template for the synthesis of aminocyclitols

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; AZABICYCLO DERIVATIVE; CYCLITOL;

EID: 54049158949     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol801381t     Document Type: Article
Times cited : (76)

References (46)
  • 2
    • 34249322373 scopus 로고    scopus 로고
    • and references cited therein. For biological properties of conduramines, see
    • (a) For biological properties of conduramines, see: Lysek, R.; Favre, S.; Vogel, P. Tetrahedron 2007, 63, 6558-6572, and references cited therein.
    • (2007) Tetrahedron , vol.63 , pp. 6558-6572
    • Lysek, R.1    Favre, S.2    Vogel, P.3
  • 28
  • 31
    • 0030727608 scopus 로고    scopus 로고
    • The observed NMR splitting pattern in 6 is because of restricted rotation about the NCO bond (rotamers). For similar observations, see: Pavri, N. P.; Trudell, M. L. Tetrahedron Lett. 1997, 38, 7993-7996.
    • The observed NMR splitting pattern in 6 is because of restricted rotation about the NCO bond (rotamers). For similar observations, see: Pavri, N. P.; Trudell, M. L. Tetrahedron Lett. 1997, 38, 7993-7996.
  • 34
    • 61349117871 scopus 로고    scopus 로고
    • Crystallographic data for the structure reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-691970
    • Crystallographic data for the structure reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-691970.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.