Park HG - Search Results

1

Highly enantioselective synthesis of (2S)-alpha-(hydroxymethyl)-glutamic acid by the catalytic Michael addition of 2-naphthalen-1-yl-2-oxazoline-4-carboxylic acid tert-butyl ester.

Lee YJ, Lee J, Kim MJ, Jeong BS, Lee JH, Kim TS, Lee J, Ku JM, Jew SS, Park HG. Lee YJ, et al. Among authors: park hg. Org Lett. 2005 Jul 21;7(15):3207-9. doi: 10.1021/ol050920s. Org Lett. 2005. PMID: 16018622

2

Highly enantioselective and practical cinchona-derived phase-transfer catalysts for the synthesis of alpha-amino acids.

Park HG, Jeong BS, Yoo MS, Lee JH, Park MK, Lee YJ, Kim MJ, Jew SS. Park HG, et al. Among authors: park mk. Angew Chem Int Ed Engl. 2002 Aug 16;41(16):3036-8. doi: 10.1002/1521-3773(20020816)41:16<3036::AID-ANIE3036>3.0.CO;2-3. Angew Chem Int Ed Engl. 2002. PMID: 12203450 No abstract available.

3

An unusual electronic effect of an aromatic-F in phase-transfer catalysts derived from cinchona-alkaloid.

Jew SS, Yoo MS, Jeong BS, Park IY, Park HG. Jew SS, et al. Among authors: park iy, park hg. Org Lett. 2002 Nov 28;4(24):4245-8. doi: 10.1021/ol0267679. Org Lett. 2002. PMID: 12443069

4

Synthesis of 2-substituted-pyrrolidinethiourea derivatives and their antagonist effect on vanilloid receptor.

Park Hg, Park Mk, Choi Jy, Choi Sh, Lee J, Suh Yg, Oh U, Lee J, Kim HD, Park YH, Jeong YS, Choi JK, Jew Ss. Park Hg, et al. Among authors: park yh, park mk. Bioorg Med Chem Lett. 2003 Jan 20;13(2):197-200. doi: 10.1016/s0960-894x(02)00887-9. Bioorg Med Chem Lett. 2003. PMID: 12482422

5

Synthesis of N,N',N"-trisubstituted thiourea derivatives and their antagonist effect on the vanilloid receptor.

Park HG, Park MK, Choi JY, Choi SH, Lee J, Park BS, Kim MG, Suh YG, Cho H, Oh U, Lee J, Kim HD, Park YH, Koh HJ, Lim KM, Moh JH, Jew SS. Park HG, et al. Among authors: park bs, park yh, park mk. Bioorg Med Chem Lett. 2003 Feb 24;13(4):601-4. doi: 10.1016/s0960-894x(02)01040-5. Bioorg Med Chem Lett. 2003. PMID: 12639539

6

Synthesis of 6-formyl-pyridine-2-carboxylate derivatives and their telomerase inhibitory activities.

Jew SS, Park BS, Lim DY, Kim MG, Chung IK, Kim JH, Hong CI, Kim JK, Park HJ, Lee JH, Park HG. Jew SS, et al. Among authors: park bs, park hg, park hj. Bioorg Med Chem Lett. 2003 Feb 24;13(4):609-12. doi: 10.1016/s0960-894x(02)01041-7. Bioorg Med Chem Lett. 2003. PMID: 12639541

7

Highly enantioselective synthesis of alpha-alkyl-alanines via the catalytic phase-transfer alkylation of 2-naphthyl aldimine tert-butyl ester by using O(9)-allyl-N(1)-2',3',4'-trifluorobenzylhydrocinchonidinium bromide.

Jew SS, Jeong BS, Lee JH, Yoo MS, Lee YJ, Park BS, Kim MG, Park HG. Jew SS, et al. Among authors: park bs, park hg. J Org Chem. 2003 May 30;68(11):4514-6. doi: 10.1021/jo034006t. J Org Chem. 2003. PMID: 12762758

8

First asymmetric total synthesis of (-)-antofine by using an enantioselective catalytic phase transfer alkylation.

Kim S, Lee J, Lee T, Park HG, Kim D. Kim S, et al. Among authors: park hg. Org Lett. 2003 Jul 24;5(15):2703-6. doi: 10.1021/ol0349007. Org Lett. 2003. PMID: 12868894

9

N-4-Substituted-benzyl-N'-tert-butylbenzyl thioureas as vanilloid receptor ligands: investigation on the role of methanesulfonamido group in antagonistic activity.

Park HG, Choi JY, Choi SH, Park MK, Lee J, Suh YG, Cho H, Oh U, Lee J, Kang SU, Lee J, Kim HD, Park YH, Su Jeong Y, Kyu Choi J, Jew SS. Park HG, et al. Among authors: park yh, park mk. Bioorg Med Chem Lett. 2004 Feb 9;14(3):787-91. doi: 10.1016/j.bmcl.2003.11.019. Bioorg Med Chem Lett. 2004. PMID: 14741290

10

N-4-methansulfonamidobenzyl-N'-2-substituted-4-tert-butyl-benzyl thioureas as potent vanilloid receptor antagonistic ligands.

Park HG, Choi JY, Choi SH, Park MK, Lee J, Suh YG, Cho H, Oh U, Kim HD, Joo YH, Kim SY, Park YH, Jeong YS, Choi JK, Kim JK, Jew SS. Park HG, et al. Among authors: park yh, park mk. Bioorg Med Chem Lett. 2004 Apr 5;14(7):1693-6. doi: 10.1016/j.bmcl.2004.01.041. Bioorg Med Chem Lett. 2004. PMID: 15026052

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