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Volumn , Issue 1, 1996, Pages 64-70

Synthesis of aliphatic 1,3-dinitro compounds

Author keywords

1,3 dicarbonyl sugar derivative; 1,3 dinitro compounds; heterocycles; Michael reaction; nitroalkenes

Indexed keywords

NITRO DERIVATIVE;

EID: 4243333724     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (6)

References (24)
  • 6
    • 0000851805 scopus 로고
    • Fleming, I.; Trost, B.M., Eds.; Pergamon: Oxford
    • Rosini, G. In Comprehensive Organic Synthesis, Vol. 2; Fleming, I.; Trost, B.M., Eds.; Pergamon: Oxford, 1991; p321.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 321
    • Rosini, G.1
  • 9
    • 0003523867 scopus 로고
    • Lambert, A.; Piggot, H. A. J. Chem. Soc. 1947, 1489. Bahner, C. T.; Kite, H. T. J. Am. Chem. Soc. 1949, 71, 3597. Snyder, H. R.; Hamlin, W. E. J. Am. Chem. Soc. 1950, 72, 5082. Shoemaker, G. L.; Keovin, R. W. J. Am. Chem. Soc. 1954, 76, 6374. Feuer, H.; Miller, R. J. Org. Chem. 1961, 26, 1348.
    • (1947) J. Chem. Soc. , pp. 1489
    • Lambert, A.1    Piggot, H.A.2
  • 10
    • 9044240501 scopus 로고
    • Lambert, A.; Piggot, H. A. J. Chem. Soc. 1947, 1489. Bahner, C. T.; Kite, H. T. J. Am. Chem. Soc. 1949, 71, 3597. Snyder, H. R.; Hamlin, W. E. J. Am. Chem. Soc. 1950, 72, 5082. Shoemaker, G. L.; Keovin, R. W. J. Am. Chem. Soc. 1954, 76, 6374. Feuer, H.; Miller, R. J. Org. Chem. 1961, 26, 1348.
    • (1949) J. Am. Chem. Soc. , vol.71 , pp. 3597
    • Bahner, C.T.1    Kite, H.T.2
  • 11
    • 9044232536 scopus 로고
    • Lambert, A.; Piggot, H. A. J. Chem. Soc. 1947, 1489. Bahner, C. T.; Kite, H. T. J. Am. Chem. Soc. 1949, 71, 3597. Snyder, H. R.; Hamlin, W. E. J. Am. Chem. Soc. 1950, 72, 5082. Shoemaker, G. L.; Keovin, R. W. J. Am. Chem. Soc. 1954, 76, 6374. Feuer, H.; Miller, R. J. Org. Chem. 1961, 26, 1348.
    • (1950) J. Am. Chem. Soc. , vol.72 , pp. 5082
    • Snyder, H.R.1    Hamlin, W.E.2
  • 12
    • 9044251235 scopus 로고
    • Lambert, A.; Piggot, H. A. J. Chem. Soc. 1947, 1489. Bahner, C. T.; Kite, H. T. J. Am. Chem. Soc. 1949, 71, 3597. Snyder, H. R.; Hamlin, W. E. J. Am. Chem. Soc. 1950, 72, 5082. Shoemaker, G. L.; Keovin, R. W. J. Am. Chem. Soc. 1954, 76, 6374. Feuer, H.; Miller, R. J. Org. Chem. 1961, 26, 1348.
    • (1954) J. Am. Chem. Soc. , vol.76 , pp. 6374
    • Shoemaker, G.L.1    Keovin, R.W.2
  • 13
    • 0343652673 scopus 로고
    • Lambert, A.; Piggot, H. A. J. Chem. Soc. 1947, 1489. Bahner, C. T.; Kite, H. T. J. Am. Chem. Soc. 1949, 71, 3597. Snyder, H. R.; Hamlin, W. E. J. Am. Chem. Soc. 1950, 72, 5082. Shoemaker, G. L.; Keovin, R. W. J. Am. Chem. Soc. 1954, 76, 6374. Feuer, H.; Miller, R. J. Org. Chem. 1961, 26, 1348.
    • (1961) J. Org. Chem. , vol.26 , pp. 1348
    • Feuer, H.1    Miller, R.2
  • 16
    • 9044252017 scopus 로고
    • Ph. D. Thesis, Universidad de Sevilla, Seville Spain
    • Derri Alcántara, M. P., Ph. D. Thesis, Universidad de Sevilla, Seville Spain, 1993.
    • (1993)
    • Derri Alcántara, M.P.1
  • 20
    • 9044223690 scopus 로고    scopus 로고
    • Compounds 5e and 5f were prepared starting from 4-methoxybenzaldehyde and furfural, respectively, as described for 5d in Ref. 11
    • Compounds 5e and 5f were prepared starting from 4-methoxybenzaldehyde and furfural, respectively, as described for 5d in Ref. 11.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.