메뉴 건너뛰기




Volumn 8, Issue 5, 2005, Pages 775-788

New developments in nucleophilic additions to nitrones

Author keywords

Aminoacids; Aminoalcohols; Hydroxylamines; Nitrones; Nucleophilic additions; Nucleosides

Indexed keywords

AMINO ACID; AMINOALCOHOL; ANTIFUNGAL AGENT; CARBOHYDRATE; GLYCERALDEHYDE; ISOXAZOLIDINE DERIVATIVE; ISOXAZOLIDINYL NUCLEOSIDE; NITRONE DERIVATIVE; NUCLEOSIDE ANALOG; POLYOXIN J; SERINE; THYMINE POLYOXIN C; UNCLASSIFIED DRUG;

EID: 18744414266     PISSN: 16310748     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.crci.2005.02.013     Document Type: Article
Times cited : (76)

References (55)
  • 1
    • 18744403152 scopus 로고    scopus 로고
    • Science of Synthesis
    • A. Padwa D. Bellus (Eds.). George Thieme Verlag Stuttgart (Chapter 13)
    • P. Merino Science of Synthesis in: A. Padwa D. Bellus (Eds.). Houben-Weyl Methods of Molecular Transformations, vol. 27 2004 George Thieme Verlag Stuttgart (Chapter 13) p. 511
    • (2004) Houben-Weyl Methods of Molecular Transformations , vol.27 , pp. 511
    • Merino, P.1
  • 2
    • 0002108906 scopus 로고
    • 1,3-Dipolar cycloaddition chemistry
    • A. Padwa (Ed.) Wiley, New York
    • (a) J.J. Tufariello, 1,3-Dipolar cycloaddition chemistry, in: A. Padwa (Ed.), Cycloaddition Chemistry, vol. 2, Wiley, New York, 1984, pp. 83
    • (1984) Cycloaddition Chemistry , vol.2 , pp. 83
    • Tufariello, J.J.1
  • 6
    • 0001357078 scopus 로고    scopus 로고
    • O.A. Attanasi, D. Spinelli (Eds.) Italian Society of Chemistry, Rome
    • (c) U. Chiacchio, A. Rescifina, G. Romeo, in: O.A. Attanasi, D. Spinelli (Eds.), Targets in Heterocyclic Systems, vol. 1, Italian Society of Chemistry, Rome, 1997, p. 225
    • (1997) Targets in Heterocyclic Systems , vol.1 , pp. 225
    • Chiacchio, U.1    Rescifina, A.2    Romeo, G.3
  • 15
    • 84985553225 scopus 로고
    • In this work we use the syn/anti nomenclature according to Masamune convention. See
    • (a) In this work we use the syn/anti nomenclature according to Masamune convention. See: S. Masamune, S.A. Ali, D.L. Snitman, D.S. Garvey, Angew. Chem., Int. Ed. Engl. 19 (1980) 557
    • (1980) Angew. Chem., Int. Ed. Engl. , vol.19 , pp. 557
    • Masamune, S.1    Ali, S.A.2    Snitman, D.L.3    Garvey, D.S.4
  • 23
    • 18744393515 scopus 로고    scopus 로고
    • For a recent review on diversity-oriented synthesis see
    • For a recent review on diversity-oriented synthesis see: M.D. Burke, S.L. Schreiber Angew. Chem. Int. Ed. Engl. 43 2004 43
    • (2004) Angew. Chem. Int. Ed. Engl. , vol.43 , pp. 43
    • Burke, M.D.1    Schreiber, S.L.2
  • 32
  • 42
    • 18744376113 scopus 로고    scopus 로고
    • We thank Professor Isono (Japan) for a gift of natural Polyoxin J. February
    • We thank Professor Isono (Japan) for a gift of natural Polyoxin J. February (1996).
    • (1996)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.