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Volumn 60, Issue 22, 2004, Pages 4837-4860

Dibromomethane as one-carbon source in organic synthesis: A versatile methodology to prepare the cyclic and acyclic α-methylene or α-keto acid derivatives from the corresponding terminal alkenes

Author keywords

Keto esters; Keto lactones; Methylenation; Methylene esters; Methylene lactams; Methylene lactones; Substituted acroleins; Ozonides

Indexed keywords

2 OXOACID; ACROLEIN; DIBROMOMETHANE; ESTER DERIVATIVE; LACTAM; LACTAM DERIVATIVE; LACTONE DERIVATIVE;

EID: 2342620626     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.04.013     Document Type: Article
Times cited : (39)

References (91)
  • 6
    • 0023679088 scopus 로고
    • Using methylenedimethylaminoammonium chloride, please see: (a)
    • Using methylenedimethylaminoammonium chloride, please see: (a) Takano S., Iwabichi Y., Ogasawara K. Chem. Commun. 1988;1204-1206
    • (1988) Chem. Commun. , pp. 1204-1206
    • Takano, S.1    Iwabichi, Y.2    Ogasawara, K.3
  • 40
    • 0025241833 scopus 로고
    • For oxidation of α-hydroxy esters or their equivalents, see: (a)
    • For oxidation of α-hydroxy esters or their equivalents, see: (a) Burkhardt J.P., Peet N.P., Bey P. Tetrahedron Lett. 31:1990;1385-1388
    • (1990) Tetrahedron Lett. , vol.31 , pp. 1385-1388
    • Burkhardt, J.P.1    Peet, N.P.2    Bey, P.3
  • 43
    • 33845184924 scopus 로고
    • For oxidative cleavage of the double bond of α,β-unsaturated carbonyl compounds, see: (d)
    • For oxidative cleavage of the double bond of α, β-unsaturated carbonyl compounds, see: (d) Angelastro M.R., Peet N.P., Bey P. J. Org. Chem. 54:1989;3913-3916
    • (1989) J. Org. Chem. , vol.54 , pp. 3913-3916
    • Angelastro, M.R.1    Peet, N.P.2    Bey, P.3
  • 45
    • 0347818442 scopus 로고
    • For α-oxidation of carbonyl groups, see: (f)
    • For α-oxidation of carbonyl groups, see: (f) Sliwa H., Tartar A. J. Org. Chem. 41:1976;160-163
    • (1976) J. Org. Chem. , vol.41 , pp. 160-163
    • Sliwa, H.1    Tartar, A.2
  • 55
    • 0004101860 scopus 로고
    • Padwa A. New York: Wiley. Chapter 4
    • Padwa A. 1, 3-Dipolar Cycloaddition Chemistry. Vol. 1:1984;Wiley, New York. Chapter 4
    • (1984) 1,3-Dipolar Cycloaddition Chemistry , vol.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.