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Volumn , Issue 8, 1999, Pages 1265-1267

Iminophosphoranes in heterocyclic chemistry. A simple one-pot synthesis of dihydropyrimidines and pyrimidines

Author keywords

8 pyrimidines; Amidines; Condensation reactions, dihydropyrimidines; Nitrogen ylids

Indexed keywords

ALDEHYDE DERIVATIVE; AMIDINE; DIHYDROPYRIMIDINE DERIVATIVE; HETEROCYCLIC COMPOUND; N TRIPHENYLPHOSPHORANILIDEN BENZAMIDINE; PYRIMIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0032792704     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1999-2795     Document Type: Article
Times cited : (22)

References (35)
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    • For some of recent leading references see: a) Okawa, T.; Eguchi, S. Tetrahedron 1998, 54, 5853.
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    • Okawa, T.1    Eguchi, S.2
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    • α,β-Unsaturated aldehydes 2a-e and 2j are commercially available, 2f-i and 2k-l were prepared according to the following references: 2f-g : Babler, J. H. Synth. Commun. 1982, 12, 839; 2h: Heilbron, I.; Jones, E. R. H.; Richardson, R. W.; Sondheimer, F. J. Chem. Soc. 1949, 737; 2i: Braude, E. A.; Evans, E. A. J. Chem. Soc. 1955, 3334; 2k: Piancatelli, G.; D'Ottavi, G.; Scettri, A. Ann. Chim. 1972, 62, 394; 21: Sundin, A.; Frejd, T.; Magnusson, G. J. Org. Chem. 1986, 51, 3927.
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  • 26
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    • α,β-Unsaturated aldehydes 2a-e and 2j are commercially available, 2f-i and 2k-l were prepared according to the following references: 2f-g : Babler, J. H. Synth. Commun. 1982, 12, 839; 2h: Heilbron, I.; Jones, E. R. H.; Richardson, R. W.; Sondheimer, F. J. Chem. Soc. 1949, 737; 2i: Braude, E. A.; Evans, E. A. J. Chem. Soc. 1955, 3334; 2k: Piancatelli, G.; D'Ottavi, G.; Scettri, A. Ann. Chim. 1972, 62, 394; 21: Sundin, A.; Frejd, T.; Magnusson, G. J. Org. Chem. 1986, 51, 3927.
    • (1949) J. Chem. Soc. , pp. 737
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  • 27
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    • α,β-Unsaturated aldehydes 2a-e and 2j are commercially available, 2f-i and 2k-l were prepared according to the following references: 2f-g : Babler, J. H. Synth. Commun. 1982, 12, 839; 2h: Heilbron, I.; Jones, E. R. H.; Richardson, R. W.; Sondheimer, F. J. Chem. Soc. 1949, 737; 2i: Braude, E. A.; Evans, E. A. J. Chem. Soc. 1955, 3334; 2k: Piancatelli, G.; D'Ottavi, G.; Scettri, A. Ann. Chim. 1972, 62, 394; 21: Sundin, A.; Frejd, T.; Magnusson, G. J. Org. Chem. 1986, 51, 3927.
    • (1955) J. Chem. Soc. , pp. 3334
    • Braude, E.A.1    Evans, E.A.2
  • 28
    • 0345220717 scopus 로고
    • α,β-Unsaturated aldehydes 2a-e and 2j are commercially available, 2f-i and 2k-l were prepared according to the following references: 2f-g : Babler, J. H. Synth. Commun. 1982, 12, 839; 2h: Heilbron, I.; Jones, E. R. H.; Richardson, R. W.; Sondheimer, F. J. Chem. Soc. 1949, 737; 2i: Braude, E. A.; Evans, E. A. J. Chem. Soc. 1955, 3334; 2k: Piancatelli, G.; D'Ottavi, G.; Scettri, A. Ann. Chim. 1972, 62, 394; 21: Sundin, A.; Frejd, T.; Magnusson, G. J. Org. Chem. 1986, 51, 3927.
    • (1972) Ann. Chim. , vol.62 , pp. 394
    • Piancatelli, G.1    D'Ottavi, G.2    Scettri, A.3
  • 29
    • 0011932504 scopus 로고
    • α,β-Unsaturated aldehydes 2a-e and 2j are commercially available, 2f-i and 2k-l were prepared according to the following references: 2f-g : Babler, J. H. Synth. Commun. 1982, 12, 839; 2h: Heilbron, I.; Jones, E. R. H.; Richardson, R. W.; Sondheimer, F. J. Chem. Soc. 1949, 737; 2i: Braude, E. A.; Evans, E. A. J. Chem. Soc. 1955, 3334; 2k: Piancatelli, G.; D'Ottavi, G.; Scettri, A. Ann. Chim. 1972, 62, 394; 21: Sundin, A.; Frejd, T.; Magnusson, G. J. Org. Chem. 1986, 51, 3927.
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    • note
    • 13C-NMR δ 25.9, 47.7, 108.4, 127.1, 129.0, 130.1, 131.3, 134.7, 155.0.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.