-
1
-
-
0026098727
-
Synthesis of (±)-2-oxa-carbocyclic-2,3-dideoxynucleosides as potential anti-HIV agents
-
Bamford, M. J., Humber, D. C., and Storer, R. Synthesis of (±)-2-oxa-carbocyclic-2,3-dideoxynucleosides as potential anti-HIV agents. Tetrahedron Lett., 32, 271-274 (1991).
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 271-274
-
-
Bamford, M.J.1
Humber, D.C.2
Storer, R.3
-
2
-
-
0026534342
-
Synthesis of Enantiomerically Pure (2R,5S)-(-)-1-(2-hydroxymethyl-L-oxathiolan-5-yl) cytosine as a Potent Antiviral Agent against Hepatitis B Virus (HBV) and Human Immunodeficiency Virus (HIV)
-
Beach, J. W., Jeong, L. S., Alves, A. J., Pohl, D., Kim, H. O., Chang, C. N., Doong, S. L., Schinazi, R. F., Cheng, Y. -C., and Chu, C. K. Synthesis of Enantiomerically Pure (2R,5S)-(-)-1-(2-hydroxymethyl-L-oxathiolan-5-yl) cytosine as a Potent Antiviral Agent against Hepatitis B Virus (HBV) and Human Immunodeficiency Virus (HIV). J. Org. Chem., 57, 2217-2219 (1992).
-
(1992)
J. Org. Chem.
, vol.57
, pp. 2217-2219
-
-
Beach, J.W.1
Jeong, L.S.2
Alves, A.J.3
Pohl, D.4
Kim, H.O.5
Chang, C.N.6
Doong, S.L.7
Schinazi, R.F.8
Cheng, Y.C.9
Chu, C.K.10
-
3
-
-
0027408378
-
Asymmetric Synthesis and Biological Evaluation of β-L-(2R,5S)- And α-L-(2R,5R)-1,3-Oxathiolanyl Pyrimidine and Purine Nucleosides as Potential Anti-HIV Agents
-
Jeong, L. S., Schinazi, Beach, R. F., Kim, H. O., Nampalli, S., Shanmuganathan, K., Alves, A. J., McMillan, A., and Chu, C. K. Asymmetric Synthesis and Biological Evaluation of β-L-(2R,5S)- and α-L-(2R,5R)-1,3-Oxathiolanyl Pyrimidine and Purine Nucleosides as Potential Anti-HIV Agents. J. Med. Chem., 36, 181-195 (1993).
-
(1993)
J. Med. Chem.
, vol.36
, pp. 181-195
-
-
Jeong, L.S.1
Schinazi2
Beach, R.F.3
Kim, H.O.4
Nampalli, S.5
Shanmuganathan, K.6
Alves, A.J.7
McMillan, A.8
Chu, C.K.9
-
4
-
-
0031823742
-
Synthesis and antiviral activity of apio dideoxynucleosides with azido or amino substituent
-
Jeong, L.S., Lee, Y. A., Moon, H. R., and Chun, M. W. Synthesis and antiviral activity of apio dideoxynucleosides with azido or amino substituent. Nucleosides & Nucleotides, 17, 1473-1478 (1998).
-
(1998)
Nucleosides & Nucleotides
, vol.17
, pp. 1473-1478
-
-
Jeong, L.S.1
Lee, Y.A.2
Moon, H.R.3
Chun, M.W.4
-
5
-
-
0035282943
-
Syntheses and Structure-Activity Relationships of Novel Apio and Thioapio Dideoxydidehydro Nucleosides as Anti-HCMV Agents
-
Jeong, L. S., Kim, H. O., Moon, H. R., Hong, J. H., Yoo, S. J., Choi, W. J., Chun, M. W., and Lee, C.-K. Syntheses and Structure-Activity Relationships of Novel Apio and Thioapio Dideoxydidehydro Nucleosides as Anti-HCMV Agents. J. Med. Chem., 44, 806-813 (2001).
-
(2001)
J. Med. Chem.
, vol.44
, pp. 806-813
-
-
Jeong, L.S.1
Kim, H.O.2
Moon, H.R.3
Hong, J.H.4
Yoo, S.J.5
Choi, W.J.6
Chun, M.W.7
Lee, C.-K.8
-
6
-
-
7344264636
-
Activities of the Four Optical Isomers of 2,3-Dideoxy-3-thiacytidine (BCH-189) against Human Immunodeficiency Virus Type 1 in Human Lymphocytes
-
Schinazi, R. F., Chu, C. K., Peck, A., McMillan, A., Mathis, R., Cannon, D., Jeong, L. S., Beach, J. W., Choi, W.-B., Yeola, S., Liotta, D. C. Activities of the Four Optical Isomers of 2,3-Dideoxy-3-thiacytidine (BCH-189) against Human Immunodeficiency Virus Type 1 in Human Lymphocytes. Antimicrob. Agents Chemother., 36, 672-676 (1992).
-
(1992)
Antimicrob. Agents Chemother.
, vol.36
, pp. 672-676
-
-
Schinazi, R.F.1
Chu, C.K.2
Peck, A.3
McMillan, A.4
Mathis, R.5
Cannon, D.6
Jeong, L.S.7
Beach, J.W.8
Choi, W.-B.9
Yeola, S.10
Liotta, D.C.11
-
7
-
-
0025909708
-
Synthesis of chiral 3-substituted γ-lactones and 9-furanosyl-adenine from (R)-2-(2,2-diethoxyethyl)-1,3-propanediol monoacetate prepared by lipase-catalyzed reaction
-
Terao, Y., Akamatsu, M., Achiwa, K. Synthesis of chiral 3-substituted γ-lactones and 9-furanosyl-adenine from (R)-2-(2,2-diethoxyethyl)-1,3-propanediol monoacetate prepared by lipase-catalyzed reaction. Chem. Pharm. Bull., 39, 823-825 (1991).
-
(1991)
Chem. Pharm. Bull.
, vol.39
, pp. 823-825
-
-
Terao, Y.1
Akamatsu, M.2
Achiwa, K.3
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