Michael E. Jung
Department of Chemistry and Biochemistry
University of California
Los Angeles
405 Hilgard Avenue
USA
Name/email consistency: high
- Enantiospecific formal total synthesis of (+)-fawcettimine. Jung, M.E., Chang, J.J. Org. Lett. (2010)
- Total synthesis of auripyrone B using a non-aldol aldol-cuprate opening process. Jung, M.E., Chaumontet, M., Salehi-Rad, R. Org. Lett. (2010)
- Studies toward the total syntheses of cucurbitacins B and D. Jung, M.E., Lui, R.M. J. Org. Chem. (2010)
- Structure-activity relationship for thiohydantoin androgen receptor antagonists for castration-resistant prostate cancer (CRPC). Jung, M.E., Ouk, S., Yoo, D., Sawyers, C.L., Chen, C., Tran, C., Wongvipat, J. J. Med. Chem. (2010)
- Synthesis of a trans,syn,trans-dodecahydrophenanthrene via a bicyclic transannular Diels-Alder reaction: intermediate for the synthesis of fusidic acid. Jung, M.E., Zhang, T.H., Lui, R.M., Gutierrez, O., Houk, K.N. J. Org. Chem. (2010)
- Synthesis of 2-substituted 7-hydroxybenzofuran-4-carboxylates via addition of silyl enol ethers to o-benzoquinone esters. Jung, M.E., Perez, F. Org. Lett. (2009)
- Total synthesis of auripyrone A using a tandem non-aldol aldol/Paterson aldol process as a key step. Jung, M.E., Salehi-Rad, R. Angew. Chem. Int. Ed. Engl. (2009)
- Total synthesis of (+/-)-kellermanoldione: stepwise cycloaddition of a functionalized diene and allenoate. Jung, M.E., Cordova, J., Murakami, M. Org. Lett. (2009)
- Total synthesis of racemic laurenditerpenol, an HIF-1 inhibitor. Jung, M.E., Im, G.Y. J. Org. Chem. (2009)
- Improved synthesis of the epoxy isoprostane phospholipid PEIPC and its reactivity with amines. Jung, M.E., Berliner, J.A., Koroniak, L., Gugiu, B.G., Watson, A.D. Org. Lett. (2008)
- Anti aldol selectivity in a synthetic approach to the C1-C12 fragment of the tedanolides. Jung, M.E., Zhang, T.H. Org. Lett. (2008)
- Facile synthesis of cis-2-Alkyl-3-trialkylsilyloxycycloalkanones via the non-aldol aldol rearrangement of 2,3-epoxycycloalkanols. Jung, M.E., Allen, D.A. Org. Lett. (2008)
- Preparation of a functionalized tetracyclic intermediate for the synthesis of rhodexin A. Jung, M.E., Chu, H.V. Org. Lett. (2008)
- Synthesis of the C1-C12 fragment of the tedanolides. Aldol-non-aldol aldol approach. Jung, M.E., Yoo, D. Org. Lett. (2007)
- Total synthesis of (+/-)-hedychilactone B: stepwise allenoate diene cycloaddition to prepare trimethyldecalin systems. Jung, M.E., Murakami, M. Org. Lett. (2007)
- Unprecedented rearrangement of a 4-alkoxy-5-bromoalk-2-en-1-ol to a cyclopentenone via an iso-nazarov cyclization process. Jung, M.E., Yoo, D. J. Org. Chem. (2007)
- Stepwise acid-promoted double-Michael process: an alternative to Diels-Alder cycloadditions for hindered silyloxydiene-dienophile pairs. Jung, M.E., Ho, D.G. Org. Lett. (2007)
- Total synthesis of (+/-)-hedychenone: trimethyldecalin terpene systems via stepwise allenoate diene cycloaddition. Jung, M.E., Murakami, M. Org. Lett. (2006)
- Practical syntheses of dyes for difference gel electrophoresis. Jung, M.E., Kim, W.J. Bioorg. Med. Chem. (2006)
- Synthesis of highly substituted cyclohexenes via mixed Lewis acid-catalyzed Diels-Alder reactions of highly substituted dienes and dienophiles. Jung, M.E., Ho, D., Chu, H.V. Org. Lett. (2005)
- Intramolecular Diels-Alder reactions of optically active allenic ketones: chirality transfer in the preparation of substituted oxa-bridged octalones. Jung, M.E., Min, S.J. J. Am. Chem. Soc. (2005)
- Versatile diastereoselectivity in formal [3,3]-sigmatropic shifts of substituted 1-alkenyl-3-alkylidenecyclobutanols and their silyl ethers. Jung, M.E., Nishimura, N., Novack, A.R. J. Am. Chem. Soc. (2005)
- Total synthesis of the epoxy isoprostane phospholipids PEIPC and PECPC. Jung, M.E., Berliner, J.A., Angst, D., Yue, D., Koroniak, L., Watson, A.D., Li, R. Org. Lett. (2005)
- Synthesis of (2R,3S) 3-amino-4-mercapto-2-butanol, a threonine analogue for covalent inhibition of sortases. Jung, M.E., Clemens, J.J., Suree, N., Liew, C.K., Pilpa, R., Campbell, D.O., Clubb, R.T. Bioorg. Med. Chem. Lett. (2005)
- Microwave-assisted allylation of acetals with allyltrimethylsilane in the presence of CuBr. Jung, M.E., Maderna, A. J. Org. Chem. (2004)
- Synthesis and relative stability of 3,5-diacyl-4,5-dihydro-1H-pyrazoles prepared by dipolar cycloaddition of enones and alpha-diazoketones. Jung, M.E., Min, S.J., Houk, K.N., Ess, D. J. Org. Chem. (2004)
- First synthesis of the A/B ring of ouabain. Jung, M.E., Piizzi, G. Org. Lett. (2003)
- Studies towards the total synthesis of an epoxy isoprostane phospholipid, a potent activator of endothelial cells. Jung, M.E., Kers, A., Subbanagounder, G., Berliner, J.A. Chem. Commun. (Camb.) (2003)
- Synthetic approach to the AB ring system of ouabain. Jung, M.E., Piizzi, G. J. Org. Chem. (2003)
- Use of hindered silyl ethers as protecting groups for the non-aldol aldol process. Jung, M.E., Hoffmann, B., Rausch, B., Contreras, J.M. Org. Lett. (2003)
- Unexpected syn hydride migration in the non-aldol aldol reaction. Jung, M.E., van den Heuvel, A., Leach, A.G., Houk, K.N. Org. Lett. (2003)
- A tandem non-aldol aldol Mukaiyama aldol reaction. Jung, M.E., van den Heuvel, A. Org. Lett. (2003)
- Novel rearrangements of 4-silyl-3-buten-2-ones. Jung, M.E., Piizzi, G. J. Org. Chem. (2002)
- Synthetic approach to analogues of the original structure of sclerophytin A. Jung, M.E., Pontillo, J. J. Org. Chem. (2002)
- Efficient synthesis of a tricyclic BCD analogue of ouabain: Lewis acid catalyzed Diels-Alder reactions of sterically hindered systems. Jung, M.E., Davidov, P. Angew. Chem. Int. Ed. Engl. (2002)
- Conclusive evidence of the trapping of primary ozonides. Jung, M.E., Davidov, P. Org. Lett. (2001)
- Preparation of 4'-substituted thymidines by substitution of the thymidine 5'-esters. Jung, M.E., Toyota, A. J. Org. Chem. (2001)
- Enantioselective formal total synthesis of (-)-dysidiolide. Jung, M.E., Nishimura, N. Org. Lett. (2001)
- Synthesis of a fully functionalized protected C1-C11 fragment for the synthesis of the tedanolides. Jung, M.E., Lee, C.P. Org. Lett. (2001)
- The first reported anionic oxy retro-ene reaction. Jung, M.E., Davidov, P. Org. Lett. (2001)
- Efficient synthesis of the C(1)-C(11) fragment of the tedanolides. The nonaldol aldol process in synthesis. Jung, M.E., Marquez, R. Org. Lett. (2000)
- Use of optically active cyclic N,N-dialkyl aminals in asymmetric induction. Jung, M.E., Huang, A. Org. Lett. (2000)
- Unusual alpha-methylation of alkoxyaryl ketones with higher order methyl cuprate and lithium bromide. Jung, M.E., Lee, B.S. J. Org. Chem. (2000)
- Synthesis of four diastereomeric 3,5-dialkoxy-2,4-dimethylalkanals by a simple extension of the non-aldol aldol process to bis(propionates). Jung, M.E., Lee, W.S., Sun, D. Org. Lett. (1999)
- Facile preparation of allenic hydroxyketones via rearrangement of propargylic alcohols. Jung, M.E., Pontillo, J. Org. Lett. (1999)
- Efficient synthesis of 2-deoxy L-ribose from L-arabinose: mechanistic information on the 1,2-acyloxy shift in alkyl radicals. Jung, M.E., Xu, Y. Org. Lett. (1999)
- First total synthesis of xestobergsterol A and active structural analogues of the xestobergsterols. Jung, M.E., Johnson, T.W. Org. Lett. (1999)
