메뉴 건너뛰기




Volumn 26, Issue 10-12, 2007, Pages 1653-1657

Asymmetric synthesis and biological activity of l-bicyclocarba-d4T

Author keywords

(R) epichlorohydrin; Anti HIV agent; Novel L bicyclocarba d4T; Tandem alkylation

Indexed keywords

ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT; LACTONE DERIVATIVE; LEVO BICYCLOCARBA BETA 2',3' DIDEHYDRO 3' DEOXYTHYMIDINE; UNCLASSIFIED DRUG;

EID: 36949034506     PISSN: 15257770     EISSN: 15322335     Source Type: Journal    
DOI: 10.1080/15257770701615599     Document Type: Article
Times cited : (3)

References (15)
  • 2
    • 0026523623 scopus 로고
    • HIV inhibitors targeted at the reverse transcriptase
    • De Clercq, E. HIV inhibitors targeted at the reverse transcriptase. AIDS Res. Hum. Retroviruses 1992, 8, 119.
    • (1992) AIDS Res. Hum. Retroviruses , vol.8 , pp. 119
    • De Clercq, E.1
  • 3
    • 0023124801 scopus 로고
    • Both 2′,3′-dideoxythymidine and its 2′,3′-unsaturated derivative (2′,3′-dideoxythymidinene) are potent and selective inhibitors of human immunodeficiency virus replication in vitro
    • Baba, M.; Pauwels, R.; Herdewijn, P.; De Clercq, E.; Desmyter, J.; Vandeputte, M. Both 2′,3′-dideoxythymidine and its 2′,3′-unsaturated derivative (2′,3′-dideoxythymidinene) are potent and selective inhibitors of human immunodeficiency virus replication in vitro. Biochem. Biophys. Res. Commun. 1987, 142, 128-134.
    • (1987) Biochem. Biophys. Res. Commun , vol.142 , pp. 128-134
    • Baba, M.1    Pauwels, R.2    Herdewijn, P.3    De Clercq, E.4    Desmyter, J.5    Vandeputte, M.6
  • 4
    • 0025866982 scopus 로고
    • Anti-human immunodeficiency virus type 1 activity and in vitro toxicity of 2′-deoxy-3′-thiacytidine (BCH-189), a novel heterocyclic nucleoside analog
    • Soudeyns, H.; Yao, S.-J.; Gao, W.; Belleau, B.; Kraus, J.-L.; Nguyen-Ba, N.; Spira, B.; Wainberg, M.A. Anti-human immunodeficiency virus type 1 activity and in vitro toxicity of 2′-deoxy-3′-thiacytidine (BCH-189), a novel heterocyclic nucleoside analog. Antimicrob. Agents Chemother. 1991, 35, 1386-1390.
    • (1991) Antimicrob. Agents Chemother , vol.35 , pp. 1386-1390
    • Soudeyns, H.1    Yao, S.-J.2    Gao, W.3    Belleau, B.4    Kraus, J.-L.5    Nguyen-Ba, N.6    Spira, B.7    Wainberg, M.A.8
  • 6
    • 77956854664 scopus 로고    scopus 로고
    • Marquez, V.E. Carbocyclic nucleosides, In Advances in Antiviral Drug Design, ed. E.De Clercq; Jai Press Inc., Greenwich, CT; 1996, 2, pp. 89-146.
    • Marquez, V.E. Carbocyclic nucleosides, In Advances in Antiviral Drug Design, ed. E.De Clercq; Jai Press Inc., Greenwich, CT; 1996, vol. 2, pp. 89-146.
  • 7
    • 0000633066 scopus 로고    scopus 로고
    • Shin, K.J.; Moon, H.R.; George, C.; Marquez, V.E. Construction of the bicyclo[3.1.0]hexane template of a conformationally locked carbocyclic adenosine via an olefin keto-carbene cycloaddition. J. Org. Chem. 2000, 65, 2172-2178.
    • Shin, K.J.; Moon, H.R.; George, C.; Marquez, V.E. Construction of the bicyclo[3.1.0]hexane template of a conformationally locked carbocyclic adenosine via an olefin keto-carbene cycloaddition. J. Org. Chem. 2000, 65, 2172-2178.
  • 8
    • 0001257247 scopus 로고    scopus 로고
    • Synthesis of cyclo propyl-fused carbocyclic nucleosides via the regioselective opening of cyclic sulfites
    • Moon, H.R.; Kim, H.O.; Chun, M.W.; Jeong, L.S.; Marquez, V.E. Synthesis of cyclo propyl-fused carbocyclic nucleosides via the regioselective opening of cyclic sulfites. J. Org. Chem. 1999, 64, 4733-4741.
    • (1999) J. Org. Chem , vol.64 , pp. 4733-4741
    • Moon, H.R.1    Kim, H.O.2    Chun, M.W.3    Jeong, L.S.4    Marquez, V.E.5
  • 9
    • 0034736361 scopus 로고    scopus 로고
    • Moon, H.R.; Ford, H., Jr.; Marquez, V.E. A remarkably simple chemicoenzymatic approach to structurally complex bicyclo[3.1.0]hexane carbocyclic nucleosides. Org. Lett. 2000, 2, 3793-3996.
    • Moon, H.R.; Ford, H., Jr.; Marquez, V.E. A remarkably simple chemicoenzymatic approach to structurally complex bicyclo[3.1.0]hexane carbocyclic nucleosides. Org. Lett. 2000, 2, 3793-3996.
  • 11
    • 15444359037 scopus 로고    scopus 로고
    • Synthesis and antiviral activity of novel acyclic nucleosides: Discovery of a cyclopropyl nucleoside with potent inhibitory activity against herpesviruses
    • Sekiyama, T.; Hatsuya, S.; Tanaka, Y.; Uchiyama, M.; Ono, N.; Iwayama, S.; Oikawa, M.; Suzuki, K.; Okunishi, M.; Tsuji, T. Synthesis and antiviral activity of novel acyclic nucleosides: discovery of a cyclopropyl nucleoside with potent inhibitory activity against herpesviruses. J. Med. Chem. 1998, 41, 1284-1298.
    • (1998) J. Med. Chem , vol.41 , pp. 1284-1298
    • Sekiyama, T.1    Hatsuya, S.2    Tanaka, Y.3    Uchiyama, M.4    Ono, N.5    Iwayama, S.6    Oikawa, M.7    Suzuki, K.8    Okunishi, M.9    Tsuji, T.10
  • 12
    • 0033544823 scopus 로고    scopus 로고
    • A practical synthesis of antiviral cyclopropane nucleoside A-5021
    • Onishi, T.; Matsuzawa, T.; Nishi, S.; Tsuji, T. A practical synthesis of antiviral cyclopropane nucleoside A-5021. Tetrahedron Lett. 1999, 40, 8845-8847.
    • (1999) Tetrahedron Lett , vol.40 , pp. 8845-8847
    • Onishi, T.1    Matsuzawa, T.2    Nishi, S.3    Tsuji, T.4
  • 13
    • 0032580376 scopus 로고    scopus 로고
    • Recent advances in olefin metathesis and its application in organic synthesis
    • Grubbs, R.H.; Chang, S. Recent advances in olefin metathesis and its application in organic synthesis. Tetrahedron 1998, 54, 4413-4450.
    • (1998) Tetrahedron , vol.54 , pp. 4413-4450
    • Grubbs, R.H.1    Chang, S.2
  • 14
    • 3343012187 scopus 로고    scopus 로고
    • Olefin metathesis
    • Grubbs, R.H. Olefin metathesis. Tetrahedron 2004, 60, 7117-7140.
    • (2004) Tetrahedron , vol.60 , pp. 7117-7140
    • Grubbs, R.H.1
  • 15
    • 0033403349 scopus 로고    scopus 로고
    • Synthesis of conformationally restricted carbocyclic nucleosides: The role of the O(4′)-atom in the key hydration step of adenosine deaminase
    • Marquez, V.E.; Russ, P.; Alons, R.; Siddiqui, M.A.; Hernandez, S.; George, C.; Nicklaus, M.C.; Dai, F.; Ford, H., Jr. Synthesis of conformationally restricted carbocyclic nucleosides: the role of the O(4′)-atom in the key hydration step of adenosine deaminase. Helv. Chim. Acta. 1999, 82, 2119-2129.
    • (1999) Helv. Chim. Acta , vol.82 , pp. 2119-2129
    • Marquez, V.E.1    Russ, P.2    Alons, R.3    Siddiqui, M.A.4    Hernandez, S.5    George, C.6    Nicklaus, M.C.7    Dai, F.8    Ford Jr., H.9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.