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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Sang-Sup Jew

Research Institute of Pharmaceutical Sciences and College of Pharmacy

Seoul National University

Seoul 151-742

South Korea

[email]@plaza.snu.ac.kr

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Research Institute of Pharmaceutical Sciences and College of Pharmacy, Seoul National University, Seoul 151-742, South Korea. 2003 - 2005
  • College of Pharmacy, Seoul National University, Seoul 151-742, Korea. 2002

References

  1. Highly enantioselective epoxidation of 2,4-diarylenones by using dimeric cinchona phase-transfer catalysts: enhancement of enantioselectivity by surfactants. Jew, S.S., Lee, J.H., Jeong, B.S., Yoo, M.S., Kim, M.J., Lee, Y.J., Lee, J., Choi, S.H., Lee, K., Lah, M.S., Park, H.G. Angew. Chem. Int. Ed. Engl. (2005) [Pubmed]
  2. Highly enantioselective phase-transfer-catalytic alkylation of 2-phenyl-2-oxazoline-4-carboxylic acid tert-butyl ester for the asymmetric synthesis of alpha-alkyl serines. Jew, S.S., Lee, Y.J., Lee, J., Kang, M.J., Jeong, B.S., Lee, J.H., Yoo, M.S., Kim, M.J., Choi, S.H., Ku, J.M., Park, H.G. Angew. Chem. Int. Ed. Engl. (2004) [Pubmed]
  3. Synthesis of 6-formyl-pyridine-2-carboxylate derivatives and their telomerase inhibitory activities. Jew, S.S., Park, B.S., Lim, D.Y., Kim, M.G., Chung, I.K., Kim, J.H., Hong, C.I., Kim, J.K., Park, H.J., Lee, J.H., Park, H.G. Bioorg. Med. Chem. Lett. (2003) [Pubmed]
  4. 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, S.S., Jeong, B.S., Lee, J.H., Yoo, M.S., Lee, Y.J., Park, B.S., Kim, M.G., Park, H.G. J. Org. Chem. (2003) [Pubmed]
  5. An unusual electronic effect of an aromatic-F in phase-transfer catalysts derived from cinchona-alkaloid. Jew, S.S., Yoo, M.S., Jeong, B.S., Park, I.Y., Park, H.G. Org. Lett. (2002) [Pubmed]
 
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