메뉴 건너뛰기




Volumn 41, Issue 11, 2000, Pages 1695-1697

C6 substitution of inosine using hexamethylphosphorous triamide in conjunction with carbon tetrahalide or N-halosuccinimide

Author keywords

6 halopurine; Halogenation; HMPT; Inosine

Indexed keywords

6 BROMOPURINE RIBOSIDE; 6 CHLORPURINE RIBOSIDE; 6 N,N DIMETHYLADENOSINE; INOSINE; NUCLEOSIDE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0041404014     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)00051-4     Document Type: Article
Times cited : (41)

References (20)
  • 5
    • 0342952956 scopus 로고
    • For substitution reactions, see: (a) Townsend, L. B.; Tipson, R. S., Eds.; Wiley: New York
    • For substitution reactions, see: (a) Trivedi, B. K. In Nucleic Acid Chemistry. Part 4; Townsend, L. B.; Tipson, R. S., Eds.; Wiley: New York, 1991; pp. 269-273.
    • (1991) In Nucleic Acid Chemistry. , Issue.4 PART , pp. 269-273
    • Trivedi, B.K.1
  • 7
    • 0001585706 scopus 로고
    • (c) and references cited therein. Coupling reactions: (1) Cu-catalyzed:
    • (c) Robins, M. J.; Basom, G. L. Can. J. Chem. 1973, 51, 3161 and references cited therein. Coupling reactions: (1) Cu-catalyzed: Hocek, M.; Holy, A. Collect. Czech. Chem. Commun. 1999, 64, 229 and references cited therein. (2) Pd-catalyzed: Lakshman, M. K.; Keeler, J. C.; Hilmer, J. H.; Martin, J. Q. J. Am. Chem. Soc. 1999, 121, 6090. (3) Zn-catalyzed: (a) Stevenson, T. M.; Prasad, A. S. B.; Citineni, J. B.; Knochel, P. Tetrahedron Lett. 1996, 37, 8375. (b) Prasad. A. S. B.; Stevenson, T. M.; Citineni, J. B.; Nyzam, V.; Knochel, P. Tetrahedron 1997, 53, 7237. (c) Véliz, E. A.; Beal, P. A. Unpublished results.
    • (1973) Can. J. Chem. , vol.51 , pp. 3161
    • Robins, M.J.1    Basom, G.L.2
  • 8
    • 0033241273 scopus 로고    scopus 로고
    • (c) and references cited therein. (2) Pd-catalyzed:
    • (c) Robins, M. J.; Basom, G. L. Can. J. Chem. 1973, 51, 3161 and references cited therein. Coupling reactions: (1) Cu-catalyzed: Hocek, M.; Holy, A. Collect. Czech. Chem. Commun. 1999, 64, 229 and references cited therein. (2) Pd-catalyzed: Lakshman, M. K.; Keeler, J. C.; Hilmer, J. H.; Martin, J. Q. J. Am. Chem. Soc. 1999, 121, 6090. (3) Zn-catalyzed: (a) Stevenson, T. M.; Prasad, A. S. B.; Citineni, J. B.; Knochel, P. Tetrahedron Lett. 1996, 37, 8375. (b) Prasad. A. S. B.; Stevenson, T. M.; Citineni, J. B.; Nyzam, V.; Knochel, P. Tetrahedron 1997, 53, 7237. (c) Véliz, E. A.; Beal, P. A. Unpublished results.
    • (1999) Collect. Czech. Chem. Commun. , vol.64 , pp. 229
    • Hocek, M.1    Holy, A.2
  • 9
    • 0033618139 scopus 로고    scopus 로고
    • (3) Zn-catalyzed:
    • (c) Robins, M. J.; Basom, G. L. Can. J. Chem. 1973, 51, 3161 and references cited therein. Coupling reactions: (1) Cu-catalyzed: Hocek, M.; Holy, A. Collect. Czech. Chem. Commun. 1999, 64, 229 and references cited therein. (2) Pd-catalyzed: Lakshman, M. K.; Keeler, J. C.; Hilmer, J. H.; Martin, J. Q. J. Am. Chem. Soc. 1999, 121, 6090. (3) Zn-catalyzed: (a) Stevenson, T. M.; Prasad, A. S. B.; Citineni, J. B.; Knochel, P. Tetrahedron Lett. 1996, 37, 8375. (b) Prasad. A. S. B.; Stevenson, T. M.; Citineni, J. B.; Nyzam, V.; Knochel, P. Tetrahedron 1997, 53, 7237. (c) Véliz, E. A.; Beal, P. A. Unpublished results.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 6090
    • Lakshman, M.K.1    Keeler, J.C.2    Hilmer, J.H.3    Martin, J.Q.4
  • 13
    • 0002779608 scopus 로고
    • and references cited therein.
    • Castro, B. R. Org. React. 1983, 29, 1 and references cited therein.
    • (1983) Org. React. , vol.29 , pp. 1
    • Castro, B.R.1
  • 14
  • 15
    • 0033582664 scopus 로고    scopus 로고
    • and references cited therein.
    • He, F.; Snider, B. B. J. Org. Chem. 1999, 64, 1397 and references cited therein.
    • (1999) J. Org. Chem. , vol.64 , pp. 1397
    • He, F.1    Snider, B.B.2
  • 17
    • 0013843406 scopus 로고    scopus 로고
    • 31P NMR resonance reported for an aryloxyphosphonium salt: 38.5 ppm, Ramirez, F.; Patwardhan, A. V.; Smith, C. P. J. Am. Chem. Soc. 1965, 87, 4973.
    • 31P NMR resonance reported for an aryloxyphosphonium salt: 38.5 ppm, Ramirez, F.; Patwardhan, A. V.; Smith, C. P. J. Am. Chem. Soc. 1965, 87, 4973.
  • 18
    • 0343388375 scopus 로고    scopus 로고
    • 13C NMR, MS, and HRMS).
    • 13C NMR, MS, and HRMS).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.