메뉴 건너뛰기




Volumn 76, Issue 3, 2004, Pages 603-613

New methods for the synthesis of heterocyclic compounds

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; ALKYL GROUP; AZIRIDINE DERIVATIVE; FUNCTIONAL GROUP; HETEROCYCLIC COMPOUND; NITROGEN; ORGANIC COMPOUND; PHOSPHINE DERIVATIVE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE;

EID: 2442674420     PISSN: 00334545     EISSN: None     Source Type: Journal    
DOI: 10.1351/pac200476030603     Document Type: Conference Paper
Times cited : (14)

References (73)
  • 9
    • 37549054627 scopus 로고    scopus 로고
    • G. W. Gribble and T. L. Gilchrist (Eds.), Chap. 4, Elsevier Science, Oxford
    • A. Padwa and S. S. Murphree. In Progress in Heterocyclic Chemistry, Vol. 14, G. W. Gribble and T. L. Gilchrist (Eds.), Chap. 4, Elsevier Science, Oxford (2000).
    • (2000) Progress in Heterocyclic Chemistry , vol.14
    • Padwa, A.1    Murphree, S.S.2
  • 20
    • 0003917975 scopus 로고
    • E. F. V. Scriven (Ed.), Academic Press, Orlando, and references cited therein
    • R. S. Atkinson. In Azides and Nitrenes, E. F. V. Scriven (Ed.), Academic Press, Orlando (1984) and references cited therein.
    • (1984) Azides and Nitrenes
    • Atkinson, R.S.1
  • 21
    • 0008154650 scopus 로고    scopus 로고
    • American Council on Science and Health, New York, and references cited therein
    • R. J. Daland. In Lead and Human Health: An Update, American Council on Science and Health, New York (2000) and references cited therein.
    • (2000) Lead and Human Health: An Update
    • Daland, R.J.1
  • 24
    • 2442700409 scopus 로고    scopus 로고
    • H. Lund and O. Hammerich (Eds.), Chap. 14, Marcel Dekker, New York
    • S. Torii and H. Tanaka. In Organic Electrochemistry, 4th ed., H. Lund and O. Hammerich (Eds.), Chap. 14, Marcel Dekker, New York (2001).
    • (2001) Organic Electrochemistry, 4th Ed.
    • Torii, S.1    Tanaka, H.2
  • 34
    • 33748605775 scopus 로고
    • The use of aziridines in complex molecule synthesis, see: D. Tanner. Angew. Chem., Int. Ed. Engl. 33, 599-619 (1994).
    • (1994) Angew. Chem., Int. Ed. Engl. , vol.33 , pp. 599-619
    • Tanner, D.1
  • 35
    • 2442707885 scopus 로고    scopus 로고
    • note
    • For a one-electron process, the 0.8 V anodic shift corresponds to the 18 kcal/mol increase in oxidative stability.
  • 36
    • 0003438149 scopus 로고    scopus 로고
    • Chap. 6, John Wiley, Chichester
    • For example, see: (a) P. M. Dewick. In Medicinal Natural Products, Chap. 6, John Wiley, Chichester (1997);
    • (1997) Medicinal Natural Products
    • Dewick, P.M.1
  • 46
    • 2442641605 scopus 로고    scopus 로고
    • note
    • We were able to isolate and characterize the N-Cl containing intermediate.
  • 48
    • 0035649065 scopus 로고    scopus 로고
    • For recent developments in bidentate ligands chemistry, see (a) A. Pfaltz. Chimia 55, 708-714 (2001);
    • (2001) Chimia , vol.55 , pp. 708-714
    • Pfaltz, A.1
  • 56
    • 0035649065 scopus 로고    scopus 로고
    • For allylic substitution, see (a) A. Pfaltz. Chimia 55, 708-714 (2001);
    • (2001) Chimia , vol.55 , pp. 708-714
    • Pfaltz, A.1
  • 60
    • 0000421290 scopus 로고    scopus 로고
    • E. N. Jacobsen, A. Pfaltz, H. Yamamoto (Eds.), Springer, Berlin
    • For hydrosilylation, see (e) H. Nishiyama. In Comprehensive Asymmetric Catalysis, Vol. 1, E. N. Jacobsen, A. Pfaltz, H. Yamamoto (Eds.), p. 267, Springer, Berlin (1999);
    • (1999) Comprehensive Asymmetric Catalysis , vol.1 , pp. 267
    • Nishiyama, H.1
  • 72
    • 0000350772 scopus 로고
    • For cyclohexene oxide ring-opening with diphenylphosphine, see: G. Muller and D. Sainz. J. Organomet. Chem. 495, 103-111 (1995).
    • (1995) J. Organomet. Chem. , vol.495 , pp. 103-111
    • Muller, G.1    Sainz, D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.