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Volumn 72, Issue 3, 2007, Pages 1055-1057

Synthesis of 2(1H)-pyrazinone phosphonates via an Arbuzov-type reaction

Author keywords

[No Author keywords available]

Indexed keywords

3-IODOPYRAZINONES; PHOSPHONATES; REACTION CONDITIONS;

EID: 33846935229     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo062176a     Document Type: Article
Times cited : (19)

References (37)
  • 5
    • 33846933179 scopus 로고    scopus 로고
    • Patent Application PCT/US2005/034786
    • WO /037028 A2, 2006
    • Somadossi, J.-P.; Gosselin, G.; Storer, R.; Egan, J. Patent Application PCT/US2005/034786; WO 2006/037028 A2, 2006.
    • (2006)
    • Somadossi, J.-P.1    Gosselin, G.2    Storer, R.3    Egan, J.4
  • 10
    • 32644453571 scopus 로고    scopus 로고
    • Aryl phosphonates are synthetically accessible by a wide variety of (mostly catalytic) methods: (a) Kagayama, T.; Nakano, A.; Sakaguchi, S.; Ishii, Y. Org. Lett. 2006, 8, 407-409.
    • Aryl phosphonates are synthetically accessible by a wide variety of (mostly catalytic) methods: (a) Kagayama, T.; Nakano, A.; Sakaguchi, S.; Ishii, Y. Org. Lett. 2006, 8, 407-409.
  • 18
    • 0003607090 scopus 로고
    • Kosolapoff, G. M, Maier, L, Eds, Wiley-Interscience: New York
    • (a) Organic Phosphorus Compounds; Kosolapoff, G. M., Maier, L., Eds.; Wiley-Interscience: New York, 1976.
    • (1976) Organic Phosphorus Compounds
  • 26
    • 11144313152 scopus 로고    scopus 로고
    • For a recent review on azaheterocyclic phosphonates, see
    • For a recent review on azaheterocyclic phosphonates, see: Moonen, K.; Laureyn, I.; Stevens, C. V. Chem. Rev. 2004, 104, 6177-6215.
    • (2004) Chem. Rev , vol.104 , pp. 6177-6215
    • Moonen, K.1    Laureyn, I.2    Stevens, C.V.3
  • 27
    • 0021024677 scopus 로고    scopus 로고
    • All of the 3,5-dichloropyrazinones, except 1i, were synthesized according to a procedure described previously: (a) Vekemans, J.; Pollers-Wieërs, C.; Hoornaert, G. J. J. Heterocycl. Chem. 1983, 20, 919-923.
    • All of the 3,5-dichloropyrazinones, except 1i, were synthesized according to a procedure described previously: (a) Vekemans, J.; Pollers-Wieërs, C.; Hoornaert, G. J. J. Heterocycl. Chem. 1983, 20, 919-923.
  • 29
    • 33846897569 scopus 로고    scopus 로고
    • The IUPAC numbering scheme changes in going from the dichloropyrazinones to the pyrazinone phosphonates
    • The IUPAC numbering scheme changes in going from the dichloropyrazinones to the pyrazinone phosphonates.
  • 36
    • 33846897916 scopus 로고    scopus 로고
    • See ref 3 for the synthesis of the 3,5-dibromopyrazinone
    • See ref 3 for the synthesis of the 3,5-dibromopyrazinone.
  • 37
    • 33846901739 scopus 로고    scopus 로고
    • The 5-chloro-3-iodopyrazinone was synthesized according to a procedure described in: De Borggraeve, W. M. Ph.D. Thesis, Katholieke Universiteit Leuven, 2002.
    • The 5-chloro-3-iodopyrazinone was synthesized according to a procedure described in: De Borggraeve, W. M. Ph.D. Thesis, Katholieke Universiteit Leuven, 2002.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.