Citation: Me. Jung et Cp. Lee, Synthesis of a fully functionalized protected C1-C11 fragment for the synthesis of the tedanolides, ORG LETT, 3(3), 2001, pp. 333-336
Citation: Me. Jung et al., Use of negatively reinforcing electrical brain stimulation to detect conventional and nonconventional anxiolytics as well as an anxiogenic drug, PHARM BIO B, 68(1), 2001, pp. 33-42
Citation: Me. Jung et F. Slowinski, Rhodium-catalyzed decomposition of indole-substituted alpha-diazo-beta-keto esters: three different reactions based on indole oxidation state, TETRAHEDR L, 42(39), 2001, pp. 6835-6838
Citation: Me. Jung et Tw. Johnson, First total synthesis of xestobergsterol A and active structural analoguesof the xestobergsterols, TETRAHEDRON, 57(8), 2001, pp. 1449-1481
Citation: Me. Jung et A. Toyota, Preparation of 4 '-substituted thymidines by substitution of the thymidine5 '-esters, J ORG CHEM, 66(8), 2001, pp. 2624-2635
Citation: Dj. Tantillo et al., Origins of stereoselectivity in intramolecular Diels-Alder cycloadditions of dienes and dienophiles linked by ester and amide tethers, J ORG CHEM, 66(6), 2001, pp. 1938-1940
Citation: Me. Jung et al., Sex differences in nicotine substitution to a pentylenetetrazol discriminative stimulus during ethanol withdrawal in rats, PSYCHOPHAR, 149(3), 2000, pp. 235-240
Citation: Me. Jung et al., Sex differences in the discriminative stimulus effects of m-chlorophenylpiperazine and ethanol withdrawal, PSYCHOPHAR, 149(2), 2000, pp. 170-175
Citation: H. Rhee et al., Efficient synthesis of carbocyclic nucleoside, (+/-)-homocarbovir via pi-allylpalladium complexes formation from the allyl N,N-ditosylimide substrate, NUCLEOS NUC, 19(3), 2000, pp. 619-628
Citation: Me. Jung et al., Unusual diastereoselectivity in intramolecular Diels-Alder reactions of substituted 3,5-hexadienyl acrylates. Preference for a boatlike structure of the six-atom tether due to ester overlap, ORG LETT, 2(13), 2000, pp. 1835-1837
Citation: Me. Jung et R. Marquez, Efficient synthesis of the C-1-C-11 fragment of the tedanolides. The nonaldol aldol process in synthesis, ORG LETT, 2(12), 2000, pp. 1669-1672
Authors:
Nagao, Y
Sakamoto, S
Miyakawa, K
Abe, Y
Jung, ME
Citation: Y. Nagao et al., Synthesis of 1-substituted derivatives of 2,5-diphenylsilacyclopent-3-enesand 2,5-diphenylsilacyclopentanes, NIP KAG KAI, (6), 2000, pp. 411-417
Citation: Me. Jung et Cp. Lee, Use of the non-aldol aldol process in the synthesis of the C1-C11 fragmentof the tedanolides: use of lactol ethers in place of tetrahydrofurans, TETRAHEDR L, 41(50), 2000, pp. 9719-9723
Citation: Me. Jung et A. Toyota, Efficient synthesis of several methylene-expanded oxetanocin nucleoside analogues, TETRAHEDR L, 41(19), 2000, pp. 3577-3581
Authors:
Fraser, AS
Kawasaki, AM
Jung, ME
Manoharan, M
Citation: As. Fraser et al., An efficient method for the synthesis of 2 '-O-modified nucleosides via double alkylation using cyclic sulfates, TETRAHEDR L, 41(10), 2000, pp. 1523-1526
Citation: Me. Jung et Bs. Lee, Unusual alpha-methylation of alkoxyaryl ketones with higher order methyl cuprate and lithium bromide, J ORG CHEM, 65(26), 2000, pp. 9241-9244
Citation: Swt. Choe et Me. Jung, Preparation of various C-2 branched carbohydrates using intramolecular radical reactions, CARBOHY RES, 329(4), 2000, pp. 731-744
Citation: Me. Jung et J. Pontillo, Facile preparation of allenic hydroxyketones via rearrangement of propargylic alcohols, ORG LETT, 1(3), 1999, pp. 367-369