Lak Shin Jeong
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Lak Shin Jeong has a total of 18 co-authors. Here are the top co-authors by number of shared publications:
Hea Ok Kim
Department of Bioinspired Science and Laboratory of Medicinal Chemistry, College of Pharmacy, Ewha Womans University, Seoul 120-750, Republic of Korea
4 shared publicationsHyung Ryong Moon
College of Pharmacy, Pusan National University, Busan 609-753, Republic of Korea
4 shared publicationsMoon Woo Chun
College of Pharmacy , Seoul National University , Seoul, 151–742, Korea
2 shared publications- Girish Chandra
Department of Chemistry, School of Physical and Chemical Sciences Central University of South Bihar Gaya Bihar India
1 shared publication Hong Lim
1 shared publicationHwal Suh
College of Medicine, Yonsei University, Seoul 120-752, South Korea
1 shared publication
Latest Publications
- 26 November 2011
- Published by Elsevier in Tetrahedron
- Vol. 68 (4) , 1253-1261
Stereoselective synthesis and anti-HCV activity of conformationally restricted 2′-C-substituted carbanucleosides
- 26 November 2011
- Published by Elsevier in Tetrahedron
- Vol. 68 (4) , 1253-1261
Stereoselective synthesis and anti-HCV activity of conformationally restricted 2′-C-substituted carbanucleosides
- 1 April 2001
- Published by Springer Nature in Archives of Pharmacal Research
- Vol. 24 (2) , 95-99
Synthesis and antiviral activity of fluoro-substituted apio dideoxynucleosides.
- 1 April 2001
- Published by Springer Nature in Archives of Pharmacal Research
- Vol. 24 (2) , 95-99
Synthesis and antiviral activity of fluoro-substituted apio dideoxynucleosides.
- 1 February 2001
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 11 (4) , 599-603
Synthesis and antiviral activity of novel d- and l-2′-azido-2′,3′-dideoxyribofuranosyl-4′-thiopyrimidines and purines
- 1 February 2001
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 11 (4) , 599-603
Synthesis and antiviral activity of novel d- and l-2′-azido-2′,3′-dideoxyribofuranosyl-4′-thiopyrimidines and purines
- 1 July 1999
- Published by Elsevier in Bioorganic & Medicinal Chemistry
- Vol. 7 (7) , 1467-1473
Synthesis and hybridization property of sugar and phosphate linkage modified oligonucleotides
- 1 July 1999
- Published by Elsevier in Bioorganic & Medicinal Chemistry
- Vol. 7 (7) , 1467-1473
Synthesis and hybridization property of sugar and phosphate linkage modified oligonucleotides
- 1 August 1998
- Published by Taylor & Francis in Nucleosides and Nucleotides
- Vol. 17 (8) , 1473-1487
Synthesis and Antiviral Activity of Apio Dideoxy Nucleosides with Azido or Amino Substituent
Novel apio dideoxynucleosides with azido or amino substituent were synthesized starting from 1,3-dihydroxyacetone utilizing an acid-catalyzed 1,4-conjugated addition as a key step and evaluated for antiviral activity. Unfortunately, they were found to be neither active against HTV-1, HSV-1,2 and poliovirus nor toxic.
- 1 August 1998
- Published by Taylor & Francis in Nucleosides and Nucleotides
- Vol. 17 (8) , 1473-1487
Synthesis and Antiviral Activity of Apio Dideoxy Nucleosides with Azido or Amino Substituent
Novel apio dideoxynucleosides with azido or amino substituent were synthesized starting from 1,3-dihydroxyacetone utilizing an acid-catalyzed 1,4-conjugated addition as a key step and evaluated for antiviral activity. Unfortunately, they were found to be neither active against HTV-1, HSV-1,2 and poliovirus nor toxic.
- 1 June 1998
- Published by Springer Nature in Archives of Pharmacal Research
- Vol. 21 (3) , 338-343
Synthesis and antiviral activity of 2′-fluorohexopyranosyl nucleosides
2′-Fluorohexopyranosyl nucleosides1a and1b which contained a bioisosteric double bond and a fluorine were synthesized in 12 steps, starting from D-galactose. During diethylaminosulfur trifluoride (DAST) fluorination, retention of stereochemistry was observed through the participation of methoxy or chloro group at the 6-position of the purine base. The final nucleosides1a and1b were found to be inactive against HIV-1 and HSV-1,2.
- 1 June 1998
- Published by Springer Nature in Archives of Pharmacal Research
- Vol. 21 (3) , 338-343
Synthesis and antiviral activity of 2′-fluorohexopyranosyl nucleosides
2′-Fluorohexopyranosyl nucleosides1a and1b which contained a bioisosteric double bond and a fluorine were synthesized in 12 steps, starting from D-galactose. During diethylaminosulfur trifluoride (DAST) fluorination, retention of stereochemistry was observed through the participation of methoxy or chloro group at the 6-position of the purine base. The final nucleosides1a and1b were found to be inactive against HIV-1 and HSV-1,2.