메뉴 건너뛰기




Volumn 64, Issue 34, 2008, Pages 8010-8015

Regioselective synthesis of 6-halomethyl-5,6-dihydro-4H-1,2-oxazines based on cyclizations of arylalkenyl-oximes

Author keywords

[No Author keywords available]

Indexed keywords

6 HALOMETHYL 5,6 DIHYDRO 4H 1,2 OXAZINE; ARYLALKENYL OXIME; OXAZINE DERIVATIVE; OXIME DERIVATIVE;

EID: 46649097989     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.05.116     Document Type: Article
Times cited : (17)

References (30)
  • 22
    • 4644225203 scopus 로고    scopus 로고
    • For a review of cyclization reactions of dianions, see:
    • For a review of cyclization reactions of dianions, see:. Langer P., and Freiberg W. Chem. Rev. 104 (2004) 4125
    • (2004) Chem. Rev. , vol.104 , pp. 4125
    • Langer, P.1    Freiberg, W.2
  • 23
    • 46649097472 scopus 로고    scopus 로고
    • note
    • CCDC-680927 (4d), CCDC-682000 (4f) and CCDC-682001 (4j) contain all crystallographic details of this publication and is available free of charge at www.ccdc.cam.ac.uk/conts/retrieving.html or can be ordered from the following address: Cambridge Crystallographic Data Centre, 12 Union Road, GB-Cambridge CB21EZ; fax: +44 1223 336 033 or deposit@ccdc.cam.ac.uk.
  • 27
    • 46649094454 scopus 로고    scopus 로고
    • The reaction of acetophenone with hydroxylamine results in the formation of the E-configured oxime:
    • The reaction of acetophenone with hydroxylamine results in the formation of the E-configured oxime:
  • 28
    • 84996393333 scopus 로고
    • For the synthesis of the Z-configured acetophenone oxime, see:
    • Janny A. Ber. Dtsch. Chem. Ges. 15 (1882) 2781 For the synthesis of the Z-configured acetophenone oxime, see:
    • (1882) Ber. Dtsch. Chem. Ges. , vol.15 , pp. 2781
    • Janny, A.1
  • 29
    • 0001535295 scopus 로고
    • For the stereochemistry of acetophenone oximes, see also:
    • Smith J.H., and Kaiser E.T. J. Org. Chem. 39 (1974) 728 For the stereochemistry of acetophenone oximes, see also:
    • (1974) J. Org. Chem. , vol.39 , pp. 728
    • Smith, J.H.1    Kaiser, E.T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.