메뉴 건너뛰기




Volumn 9, Issue 21, 2007, Pages 4379-4382

Synthesis of the antimalarial drug FR900098 utilizing the nitroso-ene reaction

Author keywords

[No Author keywords available]

Indexed keywords

3 (N ACETYL N HYDROXY)AMINOPROPYLPHOSPHONIC ACID; 3-(N-ACETYL-N-HYDROXY)AMINOPROPYLPHOSPHONIC ACID; ANTIMALARIAL AGENT; DRUG DERIVATIVE; FOSFOMYCIN; NITROSO DERIVATIVE; PHOSPHONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 35548969911     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol702082k     Document Type: Article
Times cited : (26)

References (45)
  • 2
    • 0037034009 scopus 로고    scopus 로고
    • Ridley, R. G. Nature 2002, 415, 686-693.
    • (2002) Nature , vol.415 , pp. 686-693
    • Ridley, R.G.1
  • 7
    • 35549004172 scopus 로고
    • Hydroxyaminohydrocarbonphosphonic acids
    • US Patent 4206156
    • Suita, T. K.; Takaruzuka, M. H.; Kyoto, K. H.; Nara, H. T. Hydroxyaminohydrocarbonphosphonic acids. US Patent 4206156, 1980.
    • (1980)
    • Suita, T.K.1    Takaruzuka, M.H.2    Kyoto, K.H.3    Nara, H.T.4
  • 31
    • 35549000673 scopus 로고    scopus 로고
    • Keck, G. E.; Webb, R. R.; Yates, J. B. Tetrahedron 1981, 37, 40074016.
    • Keck, G. E.; Webb, R. R.; Yates, J. B. Tetrahedron 1981, 37, 40074016.
  • 39
    • 4344568142 scopus 로고    scopus 로고
    • Lu, X. Org. Lett. 2004, 6, 2813-2815.
    • (2004) Org. Lett , vol.6 , pp. 2813-2815
    • Lu, X.1
  • 41
    • 35548967677 scopus 로고    scopus 로고
    • All computations were performed with the GAUSSIAN03 program suite Frisch, M. J, Trucks, G. W, Schlegel, H. B, Scuseria, G. E, Robb, M. A, Cheeseman, J. R, Montgomery, J. A, Jr, Vreven, T, Kudin, K. N, Burant, J. C, Millam, J. M, Iyengar, S. S, Tomasi, J, Barone, V, Mennucci, B, Cossi, M, Scalmani, C. Rega, N, Petersson, G. A, Nakatsuji, H, Hada, M, Ehara, M, Toyota, K, Fukuda, R, Hasegawa, J, Ishida, M, Nakajima, T, Honda, Y, Kitao, O, Nakai, H, Klene, M, Li, X, Knox, J. E, Hratchian, H. P, Cross, J. B, Bakken, V, Adamo, C, Jaramillo, J, Gomperts, R, Stratmann, R. E, Yazyev, O, Austin, A. J, Cammi, R, Pomelli, C, Ochterski, J. W, Ayala, P. Y, Morokuma, K, Voth, G. A, Salvador, P, Dannenberg, J. J, Zakrzewski, V. G, Dapprich, S, Daniels, A. D, Strain, M. C, Farkas, O, Malick, D. K, Rabuck, A. D, Raghavachari, K, Foresman, J. B, Ortiz, J. V, Cui, Q, Baboul, A. G, Clifford, S, Cioslowski, J, Stefanov, B. B, Liu, G, Liashen
    • All computations were performed with the GAUSSIAN03 program suite (Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Montgomery, J. A., Jr.; Vreven, T.; Kudin, K. N.; Burant, J. C.; Millam, J. M.; Iyengar, S. S.; Tomasi, J.; Barone, V.; Mennucci, B.; Cossi, M.; Scalmani, C. Rega, N.; Petersson, G. A.; Nakatsuji, H.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Klene, M.; Li, X.; Knox, J. E.; Hratchian, H. P.; Cross, J. B.; Bakken, V.; Adamo, C.; Jaramillo, J.; Gomperts, R.; Stratmann, R. E.; Yazyev, O.; Austin, A. J.; Cammi, R.; Pomelli, C.; Ochterski, J. W.; Ayala, P. Y.; Morokuma, K.; Voth, G. A.; Salvador, P.; Dannenberg, J. J.; Zakrzewski, V. G.; Dapprich, S.; Daniels, A. D.; Strain, M. C.; Farkas, O.; Malick, D. K.; Rabuck, A. D.; Raghavachari, K.; Foresman, J. B.; Ortiz, J. V.; Cui, Q.; Baboul, A. G.; Clifford, S.; Cioslowski, J.; Stefanov, B. B.; Liu, G.; Liashenko, A.; Piskorz, P.; Komaromi, I.; Martin, R. L.; Fox, D. J.; Keith, T.; Al-Laham, M. A.; Peng, C. Y.; Nanayakkara, A.; Challacombe, M.; Gill, P. M. W.; Johnson, B.; Chen, W.; Wong, M. W.; Gonzalez, C.; Pople, J. A. Gaussian 03, Revision D.02; Gaussian, Inc.: Wallingford CT, 2004)
  • 42
    • 33748588933 scopus 로고    scopus 로고
    • utilizing analytical first and second energy derivatives. Harmonic vibrational frequencies were computed to ascertain the nature of the stationary points. We used 6-31+G** basis sets for DFT and correlation- consistent cc-pVDZ for MP2 computations. The B3PW91 functional was chosen because it is more trustworthy for large molecules than other popular DFT methods see, for instance: Schreiner, P. R, Fokin, A. A, Pascal, R. A, de Meijere, A. Org. Lett. 2006, 8, 3635-3638
    • utilizing analytical first and second energy derivatives. Harmonic vibrational frequencies were computed to ascertain the nature of the stationary points. We used 6-31+G** basis sets for DFT and correlation- consistent cc-pVDZ for MP2 computations. The B3PW91 functional was chosen because it is more trustworthy for large molecules than other popular DFT methods (see, for instance: Schreiner, P. R.; Fokin, A. A.; Pascal, R. A.; de Meijere, A. Org. Lett. 2006, 8, 3635-3638).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.