| Year |
Citation |
Score |
| 2019 |
Elshan NGRD, Rettig MB, Jung ME. Synthesis of β-Amino Diaryldienones Using the Mannich Reaction. Organic Letters. PMID 31081633 DOI: 10.1021/Acs.Orglett.9B01195 |
0.41 |
|
| 2019 |
Gim HJ, Jung ME. Formation of Aryl [1-Cyano-4-(dialkylamino)butadienyl] Ketones from Pyridines Synthesis. 51: 2548-2552. DOI: 10.1055/S-0037-1611532 |
0.359 |
|
| 2019 |
Shimizu EA, Cory B, Hoang J, Castro GG, Jung ME, Vosburg DA. Aqueous Dearomatization/Diels–Alder Cascade to a Grandifloracin Precursor Journal of Chemical Education. 96: 998-1001. DOI: 10.1021/Acs.Jchemed.8B00857 |
0.301 |
|
| 2018 |
Xing Y, Zuo J, Krogstad P, Jung ME. Synthesis and Structure-Activity Relationship (SAR) Studies of Novel Pyrazolopyridine Derivatives as Inhibitors of Enterovirus Replication. Journal of Medicinal Chemistry. PMID 29346733 DOI: 10.1021/Acs.Jmedchem.7B01863 |
0.323 |
|
| 2017 |
Østergaard ME, Nichols J, Dwight TA, Lima W, Jung ME, Swayze EE, Seth PP. Fluorinated Nucleotide Modifications Modulate Allele Selectivity of SNP-Targeting Antisense Oligonucleotides. Molecular Therapy. Nucleic Acids. 7: 20-30. PMID 28624195 DOI: 10.1016/J.Omtn.2017.02.001 |
0.758 |
|
| 2016 |
Jung ME, Sun DL, Dwight TA, Yu P, Li W, Houk KN. Synthesis of 2-Ethenylcyclopropyl Aryl Ketones via Intramolecular SN2-like Displacement of an Ester. Organic Letters. PMID 27617843 DOI: 10.1021/Acs.Orglett.6B02588 |
0.827 |
|
| 2015 |
Jung ME, Roberts CA, Perez F, Pham HV, Zou L, Houk KN. Thermodynamic Control of Isomerizations of Bicyclic Radicals: Interplay of Ring Strain and Radical Stabilization. Organic Letters. PMID 26670884 DOI: 10.1021/Acs.Orglett.5B03112 |
0.733 |
|
| 2015 |
Evdokimov NM, Clark PM, Flores G, Chai T, Faull KF, Phelps ME, Witte ON, Jung ME. Development of 2-Deoxy-2-[(18)F]fluororibose for Positron Emission Tomography Imaging Liver Function in Vivo. Journal of Medicinal Chemistry. 58: 5538-47. PMID 26102222 DOI: 10.1021/Acs.Jmedchem.5B00569 |
0.68 |
|
| 2015 |
Jung ME, Sun DL. Trapping of Payne rearrangement intermediates with arylselenide anions Tetrahedron Letters. 56: 3082-3085. DOI: 10.1016/J.Tetlet.2014.11.103 |
0.442 |
|
| 2014 |
Jung ME, Lee GS. Synthesis of highly substituted adamantanones from bicyclo[3.3.1]nonanes. The Journal of Organic Chemistry. 79: 10547-52. PMID 25275940 DOI: 10.1021/Jo501368D |
0.638 |
|
| 2014 |
Østergaard ME, Dwight T, Berdeja A, Swayze EE, Jung ME, Seth PP. Comparison of duplex stabilizing properties of 2'-fluorinated nucleic acid analogues with furanose and non-furanose sugar rings. The Journal of Organic Chemistry. 79: 8877-81. PMID 25137618 DOI: 10.1021/Jo501381Q |
0.787 |
|
| 2014 |
Jung ME, Dwight TA, Vigant F, Østergaard ME, Swayze EE, Seth PP. Synthesis and duplex-stabilizing properties of fluorinated N-methanocarbathymidine analogues locked in the C3'-endo conformation. Angewandte Chemie (International Ed. in English). 53: 9893-7. PMID 25044699 DOI: 10.1002/Anie.201405283 |
0.776 |
|
| 2014 |
Clark PM, Flores G, Evdokimov NM, McCracken MN, Chai T, Nair-Gill E, O'Mahony F, Beaven SW, Faull KF, Phelps ME, Jung ME, Witte ON. Positron emission tomography probe demonstrates a striking concentration of ribose salvage in the liver. Proceedings of the National Academy of Sciences of the United States of America. 111: E2866-74. PMID 24982199 DOI: 10.1073/Pnas.1410326111 |
0.662 |
|
| 2014 |
Jung ME, Lee GS, Pham HV, Houk KN. Palladium hydride promoted stereoselective isomerization of unactivated di(exo)methylenes to endocyclic dienes. Organic Letters. 16: 2382-5. PMID 24720691 DOI: 10.1021/Ol500710V |
0.572 |
|
| 2014 |
Jung ME, Deng G. Synthesis of α-diketones from alkylaryl- and diarylalkynes using mercuric salts. Organic Letters. 16: 2142-5. PMID 24684513 DOI: 10.1021/Ol500592M |
0.343 |
|
| 2014 |
Nathanson DA, Armijo AL, Tom M, Li Z, Dimitrova E, Austin WR, Nomme J, Campbell DO, Ta L, Le TM, Lee JT, Darvish R, Gordin A, Wei L, Liao HI, ... ... Jung ME, et al. Co-targeting of convergent nucleotide biosynthetic pathways for leukemia eradication. The Journal of Experimental Medicine. 211: 473-86. PMID 24567448 DOI: 10.1084/Jem.20131738 |
0.504 |
|
| 2014 |
Evdokimov NM, Flores G, Clark PM, Phelps ME, Witte ON, Jung ME. 5-(2-[18F]fluoroethyl)-4-methylthiazole probe for positron emission tomography of the central nervous system Chemistry of Heterocyclic Compounds. 50: 303-307. DOI: 10.1007/S10593-014-1477-4 |
0.663 |
|
| 2013 |
Murphy JM, Armijo AL, Nomme J, Lee CH, Smith QA, Li Z, Campbell DO, Liao HI, Nathanson DA, Austin WR, Lee JT, Darvish R, Wei L, Wang J, Su Y, ... ... Jung ME, et al. Development of new deoxycytidine kinase inhibitors and noninvasive in vivo evaluation using positron emission tomography. Journal of Medicinal Chemistry. 56: 6696-708. PMID 23947754 DOI: 10.1021/Jm400457Y |
0.487 |
|
| 2013 |
Jung ME, Guzaev M. Studies toward the enantiospecific total synthesis of rhodexin A. The Journal of Organic Chemistry. 78: 7518-26. PMID 23834072 DOI: 10.1021/Jo400909T |
0.826 |
|
| 2013 |
Vigant F, Lee J, Hollmann A, Tanner LB, Akyol Ataman Z, Yun T, Shui G, Aguilar HC, Zhang D, Meriwether D, Roman-Sosa G, Robinson LR, Juelich TL, Buczkowski H, Chou S, ... ... Jung ME, et al. A mechanistic paradigm for broad-spectrum antivirals that target virus-cell fusion. Plos Pathogens. 9: e1003297. PMID 23637597 DOI: 10.1371/Journal.Ppat.1003297 |
0.619 |
|
| 2013 |
Jung ME, Perez F, Regan CF, Yi SW, Perron Q. Se-phenyl prop-2-eneselenoate: an ethylene equivalent for Diels-Alder reactions. Angewandte Chemie (International Ed. in English). 52: 2060-2. PMID 23315953 DOI: 10.1002/Anie.201208294 |
0.82 |
|
| 2013 |
Jung ME, Perez F, Regan CF, Yi SW, Perron Q. Corrigendum:Se-Phenyl Prop-2-eneselenoate: An Ethylene Equivalent for Diels-Alder Reactions Angewandte Chemie International Edition. 52: 11963-11963. DOI: 10.1002/Anie.201308557 |
0.808 |
|
| 2013 |
Jung ME, Perez F, Regan CF, Yi SW, Perron Q. Berichtigung:Se-Phenyl Prop-2-eneselenoate: An Ethylene Equivalent for Diels-Alder Reactions Angewandte Chemie. 125: 12181-12181. DOI: 10.1002/Ange.201308557 |
0.808 |
|
| 2012 |
Jung ME, Deng G. Synthesis of the 1-monoester of 2-ketoalkanedioic acids, for example, octyl α-ketoglutarate. The Journal of Organic Chemistry. 77: 11002-5. PMID 23163977 DOI: 10.1021/Jo302308Q |
0.333 |
|
| 2012 |
Jung ME, Guzaev M. Trimethylaluminum-triflimide complexes for the catalysis of highly hindered Diels-Alder reactions. Organic Letters. 14: 5169-71. PMID 23030499 DOI: 10.1021/Ol302172Y |
0.795 |
|
| 2012 |
Jung ME, Chang JJ. Total synthesis of the proposed structure of mycosporulone: structural revision and an unexpected retro-aldol/aldol reaction. Organic Letters. 14: 4898-901. PMID 22954011 DOI: 10.1021/Ol302234A |
0.618 |
|
| 2012 |
Stappenbeck F, Xiao W, Epperson M, Riley M, Priest A, Huang D, Nguyen K, Jung ME, Thies RS, Farouz F. Novel oxysterols activate the Hedgehog pathway and induce osteogenesis. Bioorganic & Medicinal Chemistry Letters. 22: 5893-7. PMID 22901899 DOI: 10.1016/J.Bmcl.2012.07.073 |
0.559 |
|
| 2012 |
Jung ME, Kim WJ, Avliyakulov NK, Oztug M, Haykinson MJ. Synthesis and validation of cyanine-based dyes for DIGE. Methods in Molecular Biology (Clifton, N.J.). 854: 67-85. PMID 22311754 DOI: 10.1007/978-1-61779-573-2_6 |
0.348 |
|
| 2012 |
Regan CF, Pierre F, Schwaebe MK, Haddach M, Jung ME, Ryckman DM. A facile synthesis of 5-halopyrimidine-4-carboxylic acid esters via a Minisci reaction Synlett. 443-447. DOI: 10.1055/S-0031-1290136 |
0.833 |
|
| 2012 |
Jung ME, Yi SW. Synthesis of threo-β-aminoalcohols from aminoaldehydes via chelation-controlled additions. Total synthesis of l-threo sphingosine and safingol Tetrahedron Letters. 53: 4216-4220. DOI: 10.1016/J.Tetlet.2012.05.153 |
0.425 |
|
| 2011 |
Jung ME, Koch P. An efficient synthesis of the protected carbohydrate moiety of Brasilicardin A. Organic Letters. 13: 3710-3. PMID 21678905 DOI: 10.1021/Ol2013704 |
0.365 |
|
| 2011 |
Wang H, Houk KN, Allen DA, Jung ME. Computational elucidation of the origins of reactivity and selectivity in non-aldol aldol rearrangements of cyclic epoxides. Organic Letters. 13: 3238-41. PMID 21568276 DOI: 10.1021/Ol2011488 |
0.652 |
|
| 2011 |
Jung ME, Yoo D. First total synthesis of rhodexin A. Organic Letters. 13: 2698-701. PMID 21517087 DOI: 10.1021/Ol200796R |
0.462 |
|
| 2011 |
Johnson JS, Meliton V, Kim WK, Lee KB, Wang JC, Nguyen K, Yoo D, Jung ME, Atti E, Tetradis S, Pereira RC, Magyar C, Nargizyan T, Hahn TJ, Farouz F, et al. Novel oxysterols have pro-osteogenic and anti-adipogenic effects in vitro and induce spinal fusion in vivo. Journal of Cellular Biochemistry. 112: 1673-84. PMID 21503957 DOI: 10.1002/Jcb.23082 |
0.532 |
|
| 2011 |
Jung ME, Yoo D. Correction to First Total Synthesis of Rhodexin A Organic Letters. 13: 3766-3766. DOI: 10.1021/Ol201601P |
0.367 |
|
| 2011 |
Jung ME, Koch P. Mild, selective deprotection of PMB ethers with triflic acid/1,3-dimethoxybenzene Tetrahedron Letters. 52: 6051-6054. DOI: 10.1016/J.Tetlet.2011.08.102 |
0.335 |
|
| 2011 |
Jung ME, Chu HV. Synthesis of BCD tricyclic analogues of the novel cardiac glycoside rhodexin A Tetrahedron Letters. 52: 4512-4514. DOI: 10.1016/J.Tetlet.2011.06.114 |
0.412 |
|
| 2011 |
Jung ME, Dong TA, Cai X. Improved synthesis of 4-amino-7-nitrobenz-2,1,3-oxadiazoles using NBD fluoride (NBD-F) Tetrahedron Letters. 52: 2533-2535. DOI: 10.1016/J.Tetlet.2011.02.111 |
0.794 |
|
| 2011 |
Jung ME, Yoo D. Stereoselective synthesis of a fully protected C13-C 23 fragment of tedanolide Tetrahedron. 67: 10281-10286. DOI: 10.1016/J.Tet.2011.10.024 |
0.449 |
|
| 2010 |
Kim JY, Kim D, Kang SY, Park WK, Kim HJ, Jung ME, Son EJ, Pae AN, Kim J, Lee J. Arylpiperazine-containing pyrimidine 4-carboxamide derivatives targeting serotonin 5-HT(2A), 5-HT(2C), and the serotonin transporter as a potential antidepressant. Bioorganic & Medicinal Chemistry Letters. 20: 6439-42. PMID 20933409 DOI: 10.1016/j.bmcl.2010.09.081 |
0.463 |
|
| 2010 |
Jung ME, Lui RM. Studies toward the total syntheses of cucurbitacins B and D. The Journal of Organic Chemistry. 75: 7146-58. PMID 20873743 DOI: 10.1021/Jo101242E |
0.808 |
|
| 2010 |
Jung ME, Zhang TH, Lui RM, Gutierrez O, Houk KN. Synthesis of a trans,syn,trans-dodecahydrophenanthrene via a bicyclic transannular Diels-Alder reaction: intermediate for the synthesis of fusidic acid. The Journal of Organic Chemistry. 75: 6933-40. PMID 20843028 DOI: 10.1021/Jo101533H |
0.827 |
|
| 2010 |
Jung ME, Chang JJ. Enantiospecific formal total synthesis of (+)-fawcettimine. Organic Letters. 12: 2962-5. PMID 20515058 DOI: 10.1021/Ol1009762 |
0.679 |
|
| 2010 |
Jung ME, Chaumontet M, Salehi-Rad R. Total synthesis of auripyrone B using a non-aldol aldol-cuprate opening process. Organic Letters. 12: 2872-5. PMID 20499854 DOI: 10.1021/Ol100985N |
0.785 |
|
| 2010 |
Jung ME, Salehi-Rad R. Dipyrone approach toward the synthesis of the cytotoxic natural product auripyrone A Tetrahedron Letters. 51: 4931-4933. DOI: 10.1016/J.Tetlet.2010.07.034 |
0.752 |
|
| 2010 |
Jung ME, Toyota A. ChemInform Abstract: Efficient Synthesis of Several Methylene-Expanded Oxetanocin Nucleoside Analogues. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200035196 |
0.303 |
|
| 2010 |
Jung ME, Nishimura N. ChemInform Abstract: Stereoselective Formation of Formal Exo Diels-Alder Adducts of Silyloxydienes and Allenecarboxylates. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199934053 |
0.303 |
|
| 2010 |
JUNG ME, KIANKARIMI M. ChemInform Abstract: Substituent Effects in the Intramolecular Diels-Alder Reaction of 6-Furylhexenoates. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199835037 |
0.341 |
|
| 2010 |
JUNG ME, NICHOLS CJ. ChemInform Abstract: Synthesis of Methylene-Expanded Oxetanocin Isonucleosides in Both Enantiomeric Forms. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199823224 |
0.305 |
|
| 2010 |
JUNG ME, ANGELICA S, D'AMICO DC. ChemInform Abstract: An Intramolecular Prins Double Cyclization Catalyzed by Silyl Triflates. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199819110 |
0.374 |
|
| 2010 |
JUNG ME, NICHOLS CJ. ChemInform Abstract: Highly Stereoselective Synthesis of trans,trans-4-Aryl-2,3- oxetanedimethanols: Preparation of Oxetanocin A Analogues. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199707130 |
0.363 |
|
| 2010 |
JUNG ME, VU BT. ChemInform Abstract: Complete Diastereocontrol in Intramolecular 1,3-Dipolar Cycloadditions of 2-Substituted 5-Hexenyl and 5-Heptenyl Nitrones: Application to the Synthesis of the β-Lactam Antibiotic 1β-Methylthienamycin (X) . Cheminform. 27: no-no. DOI: 10.1002/CHIN.199644130 |
0.646 |
|
| 2010 |
JUNG ME, VU BT. ChemInform Abstract: Substituent Effects on Intramolecular Dipolar Cycloadditions: The gem- Dicarboalkoxy Effect. Cheminform. 27: no-no. DOI: 10.1002/CHIN.199619140 |
0.664 |
|
| 2010 |
JUNG ME, DANSEREAU SMK. ChemInform Abstract: Benzo(H)-1,6-naphthyridine Synthesis via Intramolecular Diels-Alder Reactions of Aryl Oxazoles: Synthetic Approach to 2- Bromoleptoclinidinone. Cheminform. 26: no-no. DOI: 10.1002/CHIN.199526166 |
0.347 |
|
| 2010 |
NAGAO Y, TAKAHASHI M, ABE Y, MISONO T, JUNG ME. ChemInform Abstract: Synthesis of 1,1-Dialkoxy Derivatives of 2,5-Diphenylsilacyclopent-3- ene and 2,5-Diphenylsilacyclopentane. Cheminform. 24: no-no. DOI: 10.1002/CHIN.199352225 |
0.308 |
|
| 2010 |
JUNG ME, ZIMMERMAN CN, LOWEN GT, KHAN SI. ChemInform Abstract: Diastereocontrol in Intermolecular Diels-Alder Reactions of Allenic Lactones: Synthetic Approach to the Plaunols. Cheminform. 24: no-no. DOI: 10.1002/CHIN.199340098 |
0.314 |
|
| 2010 |
JUNG ME, SIEDEM CS. ChemInform Abstract: Efficient Synthesis of a Hexasubstituted Aromatic Ring via an Intramolecular Michael-Aldol Process: Preparation of a Late Tricyclic Intermediate for the Synthesis of Pseudopterosin A. Cheminform. 24: no-no. DOI: 10.1002/CHIN.199336267 |
0.349 |
|
| 2010 |
JUNG ME, CHOI YM. ChemInform Abstract: New Synthesis of 2-Azetines and 1-Azabutadienes and the Use of the Latter in Diels-Alder Reactions: Total Synthesis of (.+-.)-δ- Coniceine. Cheminform. 23: no-no. DOI: 10.1002/CHIN.199218169 |
0.375 |
|
| 2009 |
Jung ME, Im GY. Total synthesis of racemic laurenditerpenol, an HIF-1 inhibitor. The Journal of Organic Chemistry. 74: 8739-53. PMID 19863119 DOI: 10.1021/Jo902029X |
0.725 |
|
| 2009 |
Jung ME, Salehi-Rad R. Total synthesis of auripyrone A using a tandem non-aldol aldol/Paterson aldol process as a key step. Angewandte Chemie (International Ed. in English). 48: 8766-9. PMID 19824033 DOI: 10.1002/Anie.200904607 |
0.785 |
|
| 2009 |
Jung ME, Cordova J, Murakami M. Total synthesis of (+/-)-kellermanoldione: stepwise cycloaddition of a functionalized diene and allenoate. Organic Letters. 11: 3882-5. PMID 19655733 DOI: 10.1021/Ol901455Q |
0.694 |
|
| 2009 |
Suree N, Liew CK, Villareal VA, Thieu W, Fadeev EA, Clemens JJ, Jung ME, Clubb RT. The structure of the Staphylococcus aureus sortase-substrate complex reveals how the universally conserved LPXTG sorting signal is recognized. The Journal of Biological Chemistry. 284: 24465-77. PMID 19592495 DOI: 10.1074/Jbc.M109.022624 |
0.312 |
|
| 2009 |
Jung ME, Perez F. Synthesis of 2-substituted 7-hydroxybenzofuran-4-carboxylates via addition of silyl enol ethers to o-benzoquinone esters. Organic Letters. 11: 2165-7. PMID 19371072 DOI: 10.1021/Ol900416X |
0.753 |
|
| 2009 |
Jung ME, Allen DA. Use of 4-cyanocoumarins as dienophiles in a facile synthesis of highly substituted dibenzopyranones. Organic Letters. 11: 757-60. PMID 19138152 DOI: 10.1021/Ol802792G |
0.675 |
|
| 2008 |
Jung ME, Berliner JA, Koroniak L, Gugiu BG, Watson AD. Improved synthesis of the epoxy isoprostane phospholipid PEIPC and its reactivity with amines. Organic Letters. 10: 4207-9. PMID 18754590 DOI: 10.1021/Ol8014804 |
0.425 |
|
| 2008 |
Jung ME, Chu HV. Preparation of a functionalized tetracyclic intermediate for the synthesis of rhodexin A. Organic Letters. 10: 3647-9. PMID 18642920 DOI: 10.1021/Ol801426Z |
0.472 |
|
| 2008 |
Jung ME, Allen DA. Facile synthesis of cis-2-Alkyl-3-trialkylsilyloxycycloalkanones via the non-aldol aldol rearrangement of 2,3-epoxycycloalkanols. Organic Letters. 10: 2039-41. PMID 18429620 DOI: 10.1021/Ol800423M |
0.649 |
|
| 2008 |
Zhang W, Watanabe K, Cai X, Jung ME, Tang Y, Zhan J. Identifying the minimal enzymes required for anhydrotetracycline biosynthesis. Journal of the American Chemical Society. 130: 6068-9. PMID 18422316 DOI: 10.1021/Ja800951E |
0.39 |
|
| 2008 |
Jung ME, Im GYJ. Convergent total synthesis of the racemic HIF-1 inhibitor laurenditerpenol Tetrahedron Letters. 49: 4962-4964. DOI: 10.1016/J.Tetlet.2008.05.116 |
0.693 |
|
| 2008 |
Jung ME, Yoo D. Synthesis of the C1-C12 fragment of the tedanolides. Selective hydroboration-protonation of allylic alcohol approach Tetrahedron Letters. 49: 816-819. DOI: 10.1016/J.Tetlet.2007.11.181 |
0.342 |
|
| 2007 |
Jung ME, Yoo D. Unprecedented rearrangement of a 4-alkoxy-5-bromoalk-2-en-1-ol to a cyclopentenone via an iso-nazarov cyclization process. The Journal of Organic Chemistry. 72: 8565-8. PMID 17910498 DOI: 10.1021/Jo071104W |
0.367 |
|
| 2007 |
Jung ME, Yoo D. Synthesis of the C1-C12 fragment of the tedanolides. Aldol-non-aldol aldol approach. Organic Letters. 9: 3543-6. PMID 17676748 DOI: 10.1021/Ol0714038 |
0.33 |
|
| 2007 |
Tsay JM, Trzoss M, Shi L, Kong X, Selke M, Jung ME, Weiss S. Singlet oxygen production by Peptide-coated quantum dot-photosensitizer conjugates. Journal of the American Chemical Society. 129: 6865-71. PMID 17477530 DOI: 10.1021/Ja070713I |
0.601 |
|
| 2007 |
Duncan MC, Ho DG, Huang J, Jung ME, Payne GS. Composite synthetic lethal identification of membrane traffic inhibitors. Proceedings of the National Academy of Sciences of the United States of America. 104: 6235-40. PMID 17404221 DOI: 10.1073/Pnas.0607773104 |
0.63 |
|
| 2007 |
Jung ME, Murakami M. Total synthesis of (+/-)-hedychilactone B: stepwise allenoate diene cycloaddition to prepare trimethyldecalin systems. Organic Letters. 9: 461-3. PMID 17249787 DOI: 10.1021/Ol062811Z |
0.46 |
|
| 2007 |
Jung ME, Ho DG. Stepwise acid-promoted double-Michael process: an alternative to Diels-Alder cycloadditions for hindered silyloxydiene-dienophile pairs. Organic Letters. 9: 375-8. PMID 17217308 DOI: 10.1021/Ol062980J |
0.744 |
|
| 2007 |
Jung ME, Murphy JM. Functional group selectivity in reactions of epoxides with tungsten hexachloride Tetrahedron Letters. 48: 8388-8391. DOI: 10.1016/J.Tetlet.2007.08.136 |
0.584 |
|
| 2007 |
Jung ME, Min SJ. Approaches to the synthesis of arisugacin A Tetrahedron. 63: 3682-3701. DOI: 10.1016/J.Tet.2007.02.085 |
0.652 |
|
| 2006 |
Jung ME, Murakami M. Total synthesis of (+/-)-hedychenone: trimethyldecalin terpene systems via stepwise allenoate diene cycloaddition. Organic Letters. 8: 5857-9. PMID 17134290 DOI: 10.1021/ol062456c |
0.382 |
|
| 2006 |
Zhao YL, Suhrada CP, Jung ME, Houk KN. Theoretical investigation of the stereoselective stepwise cope rearrangement of a 3-vinylmethylenecyclobutane. Journal of the American Chemical Society. 128: 11106-13. PMID 16925428 DOI: 10.1021/Ja060913E |
0.302 |
|
| 2006 |
Jung ME, Kim WJ. Practical syntheses of dyes for difference gel electrophoresis. Bioorganic & Medicinal Chemistry. 14: 92-7. PMID 16183291 DOI: 10.1016/J.Bmc.2005.07.068 |
0.343 |
|
| 2006 |
Jung ME, Duclos BA. Synthetic approach to analogues of betulinic acid Tetrahedron. 62: 9321-9334. DOI: 10.1016/J.Tet.2006.07.023 |
0.807 |
|
| 2005 |
Jung ME, Clemens JJ, Suree N, Liew CK, Pilpa R, Campbell DO, Clubb RT. Synthesis of (2R,3S) 3-amino-4-mercapto-2-butanol, a threonine analogue for covalent inhibition of sortases. Bioorganic & Medicinal Chemistry Letters. 15: 5076-9. PMID 16169722 DOI: 10.1016/J.Bmcl.2005.07.073 |
0.335 |
|
| 2005 |
Jung ME, Berliner JA, Angst D, Yue D, Koroniak L, Watson AD, Li R. Total synthesis of the epoxy isoprostane phospholipids PEIPC and PECPC. Organic Letters. 7: 3933-5. PMID 16119935 DOI: 10.1021/Ol051415Y |
0.449 |
|
| 2005 |
Jung ME, Nishimura N, Novack AR. Versatile diastereoselectivity in formal [3,3]-sigmatropic shifts of substituted 1-alkenyl-3-alkylidenecyclobutanols and their silyl ethers. Journal of the American Chemical Society. 127: 11206-7. PMID 16089425 DOI: 10.1021/Ja051663P |
0.819 |
|
| 2005 |
Jung ME, Min SJ. Intramolecular Diels-Alder reactions of optically active allenic ketones: chirality transfer in the preparation of substituted oxa-bridged octalones. Journal of the American Chemical Society. 127: 10834-5. PMID 16076181 DOI: 10.1021/Ja052771E |
0.666 |
|
| 2005 |
Jung ME, Ho D, Chu HV. Synthesis of highly substituted cyclohexenes via mixed Lewis acid-catalyzed Diels-Alder reactions of highly substituted dienes and dienophiles. Organic Letters. 7: 1649-51. PMID 15816774 DOI: 10.1021/Ol050361P |
0.754 |
|
| 2005 |
Jung ME, Novack AR. Formation of 3,4-dimethyl-2-pyrones from allene carboxylates and 2-silyloxydienes via 3-carboethoxyethylidene cyclobutanols Tetrahedron Letters. 46: 8237-8240. DOI: 10.1016/J.Tetlet.2005.09.091 |
0.811 |
|
| 2005 |
Jung ME, Maderna A. Synthesis of bicyclo[2.2.2]oct-5-en-2-ones via a tandem intermolecular Michael addition intramolecular aldol process (a bridged Robinson annulation) Tetrahedron Letters. 46: 5057-5061. DOI: 10.1016/J.Tetlet.2005.05.064 |
0.516 |
|
| 2004 |
Jung ME, Min SJ, Houk KN, Ess D. Synthesis and relative stability of 3,5-diacyl-4,5-dihydro-1H-pyrazoles prepared by dipolar cycloaddition of enones and alpha-diazoketones. The Journal of Organic Chemistry. 69: 9085-9. PMID 15609941 DOI: 10.1021/Jo048741W |
0.587 |
|
| 2004 |
Jung ME, Maderna A. Microwave-assisted allylation of acetals with allyltrimethylsilane in the presence of CuBr. The Journal of Organic Chemistry. 69: 7755-7. PMID 15498010 DOI: 10.1021/Jo049015W |
0.412 |
|
| 2004 |
Katz JE, Dumlao DS, Wasserman JI, Lansdown MG, Jung ME, Faull KF, Clarke S. 3-Isopropylmalate is the major endogenous substrate of the Saccharomyces cerevisiae trans-aconitate methyltransferase. Biochemistry. 43: 5976-86. PMID 15147181 DOI: 10.1021/Bi049784+ |
0.766 |
|
| 2004 |
Jung ME, Min S. Novel formation of a bridged bicyclic furan by rearrangement of a tetrahydroxydecalinone Tetrahedron Letters. 45: 6753-6755. DOI: 10.1016/J.Tetlet.2004.07.040 |
0.611 |
|
| 2004 |
Jung ME, Maderna A. Allylation of acetals and ketals with allyltrimethylsilane catalyzed by the mixed Lewis acid system AlBr3/CuBr Tetrahedron Letters. 45: 5301-5304. DOI: 10.1016/J.Tetlet.2004.04.183 |
0.518 |
|
| 2004 |
Jung ME, Duclos BA. Diastereoselectivity in the Carroll Rearrangement of β-Keto Esters of Tertiary Allylic Alcohols. Cheminform. 35. DOI: 10.1016/J.Tetlet.2003.10.102 |
0.796 |
|
| 2004 |
Jung ME, Duclos BA. Diastereoselectivity in the Carroll rearrangement of β-keto esters of tertiary allylic alcohols Tetrahedron Letters. 45: 107-109. DOI: 10.1016/j.tetlet.2003.10.102 |
0.778 |
|
| 2003 |
Jung ME, van den Heuvel A. A tandem non-aldol aldol Mukaiyama aldol reaction. Organic Letters. 5: 4705-7. PMID 14627420 DOI: 10.1021/Ol0358760 |
0.427 |
|
| 2003 |
Jung ME, van den Heuvel A, Leach AG, Houk KN. Unexpected syn hydride migration in the non-aldol aldol reaction. Organic Letters. 5: 3375-8. PMID 12967278 DOI: 10.1021/Ol0350801 |
0.435 |
|
| 2003 |
Jung ME, Hoffmann B, Rausch B, Contreras JM. Use of hindered silyl ethers as protecting groups for the non-aldol aldol process. Organic Letters. 5: 3159-61. PMID 12917006 DOI: 10.1021/Ol035295A |
0.411 |
|
| 2003 |
Leach AG, Wang R, Wohlhieter GE, Khan SI, Jung ME, Houk KN. Theoretical elucidation of kinetic and thermodynamic control of radical addition regioselectivity. Journal of the American Chemical Society. 125: 4271-8. PMID 12670249 DOI: 10.1021/Ja029342Q |
0.795 |
|
| 2003 |
Jung ME, Piizzi G. Synthetic approach to the AB ring system of ouabain. The Journal of Organic Chemistry. 68: 2572-82. PMID 12662025 DOI: 10.1021/Jo020454+ |
0.424 |
|
| 2003 |
Jung ME, Kers A, Subbanagounder G, Berliner JA. Studies towards the total synthesis of an epoxy isoprostane phospholipid, a potent activator of endothelial cells. Chemical Communications (Cambridge, England). 196-7. PMID 12585388 DOI: 10.1039/B209892J |
0.386 |
|
| 2003 |
Jung ME, Piizzi G. First synthesis of the A/B ring of ouabain. Organic Letters. 5: 137-40. PMID 12529124 DOI: 10.1021/Ol0270881 |
0.449 |
|
| 2003 |
Nagao Y, Kimura C, Kozawa K, Jung ME. Synthesis, stereochemistry, and reactions of 2,5-diphenylsilacyclopentenes Silicon Chemistry. 2: 99-107. DOI: 10.1023/B:Silc.0000047946.72949.C8 |
0.431 |
|
| 2003 |
Jung ME, Wassermann JI. Efficient Synthesis of Vinyl Chlorides and/or gem-Dichlorides from Ketones by Treatment with Tungsten Hexachloride. Cheminform. 34. DOI: 10.1016/S0040-4039(03)01884-7 |
0.36 |
|
| 2003 |
Jung ME, Wasserman JI. Efficient synthesis of vinyl chlorides and/or gem-dichlorides from ketones by treatment with tungsten hexachloride Tetrahedron Letters. 44: 7273-7275. DOI: 10.1016/S0040-4039(03)01884-7 |
0.806 |
|
| 2003 |
Jung ME, Pontillo J. Synthetic approach to potential precursors of sclerophytin A Tetrahedron. 59: 2729-2736. DOI: 10.1016/S0040-4020(03)00283-7 |
0.78 |
|
| 2003 |
Jung ME, Lyster MA. Cleavage of Methyl Ethers with Iodotrimethylsilane: Cyclohexanol from Cyclohexyl Methyl Ether Organic Syntheses. 35-35. DOI: 10.1002/0471264180.Os059.06 |
0.318 |
|
| 2003 |
Jung ME, McCombs CA. 2‐Trimethylsilyloxy‐1,3‐Butadiene as a Reactive Diene: Diethyl trans‐4‐Trimethylsilyloxy‐4‐Cyclohexene‐1,2‐Dicarboxylate Organic Syntheses. 163-163. DOI: 10.1002/0471264180.Os058.29 |
0.45 |
|
| 2002 |
Jung ME, Davidov P. Efficient synthesis of a tricyclic BCD analogue of ouabain: Lewis acid catalyzed Diels-Alder reactions of sterically hindered systems. Angewandte Chemie (International Ed. in English). 41: 4125-8. PMID 12412103 DOI: 10.1002/1521-3773(20021104)41:21<4125::Aid-Anie4125>3.0.Co;2-E |
0.823 |
|
| 2002 |
Trost BM, Chisholm JD, Wrobleski ST, Jung M. Ruthenium-catalyzed alkene-alkyne coupling: synthesis of the proposed structure of amphidinolide A. Journal of the American Chemical Society. 124: 12420-1. PMID 12381177 DOI: 10.1021/Ja027883+ |
0.304 |
|
| 2002 |
Jung ME, Pontillo J. Synthetic approach to analogues of the original structure of sclerophytin A. The Journal of Organic Chemistry. 67: 6848-51. PMID 12227825 DOI: 10.1021/Jo016246J |
0.763 |
|
| 2002 |
Jung ME, Piizzi G. Novel rearrangements of 4-silyl-3-buten-2-ones. The Journal of Organic Chemistry. 67: 3911-4. PMID 12027713 DOI: 10.1021/Jo0109467 |
0.305 |
|
| 2002 |
Jung ME, Davidov P. The first reported anionic oxy retro-ene reaction. Organic Letters. 3: 3025-7. PMID 11554834 DOI: 10.1021/Ol010154Z |
0.811 |
|
| 2002 |
Jung ME, van den Heuvel A. Diastereoselectivity in non-aldol aldol reactions: silyl triflate-promoted Payne rearrangements Tetrahedron Letters. 43: 8169-8172. DOI: 10.1016/S0040-4039(02)01890-7 |
0.466 |
|
| 2002 |
Jung ME, Toyota A, de Clercq E, Balzarini J. Synthesis and Biological Activity of a Series of Methylene-Expanded Oxetanocin Nucleoside Analogues Monatshefte F?R Chemie / Chemical Monthly. 133: 499-520. DOI: 10.1007/978-3-7091-6130-2_10 |
0.331 |
|
| 2001 |
Jung ME, Lee CP. Synthesis of a Fully Functionalized Protected C1-C11 Fragment for the Synthesis of the Tedanolides Organic Letters. 3: 333-336. PMID 11428007 DOI: 10.1021/Ol000329P |
0.336 |
|
| 2001 |
Jung ME, Nishimura N. Enantioselective formal total synthesis of (-)-dysidiolide. Organic Letters. 3: 2113-5. PMID 11418062 |
0.655 |
|
| 2001 |
Cai H, Strouse J, Dumlao D, Jung ME, Clarke S. Distinct reactions catalyzed by bacterial and yeast trans-aconitate methyltransferases. Biochemistry. 40: 2210-9. PMID 11329290 DOI: 10.1021/Bi0022902 |
0.392 |
|
| 2001 |
Jung ME, Toyota A. Preparation of 4'-substituted thymidines by substitution of the thymidine 5'-esters. The Journal of Organic Chemistry. 66: 2624-35. PMID 11304180 DOI: 10.1021/Jo001223A |
0.409 |
|
| 2001 |
Tantillo DJ, Houk KN, Jung ME. Origins of stereoselectivity in intramolecular Diels-Alder cycloadditions of dienes and dienophiles linked by ester and amide tethers. The Journal of Organic Chemistry. 66: 1938-40. PMID 11300884 DOI: 10.1021/Jo001172H |
0.418 |
|
| 2001 |
Jung ME, Davidov P. Conclusive evidence of the trapping of primary ozonides. Organic Letters. 3: 627-9. PMID 11178842 DOI: 10.1021/Ol010005G |
0.791 |
|
| 2001 |
Choe SW, Jung ME. Preparation of various C-2 branched carbohydrates using intramolecular radical reactions. Carbohydrate Research. 329: 731-44. PMID 11125815 DOI: 10.1016/S0008-6215(00)00246-9 |
0.384 |
|
| 2001 |
Jung ME, Slowinski F. Rhodium-catalyzed decomposition of indole-substituted α-diazo-β-keto esters: three different reactions based on indole oxidation state Tetrahedron Letters. 42: 6835-6838. DOI: 10.1016/S0040-4039(01)01431-9 |
0.39 |
|
| 2001 |
Jung ME, Johnson TW. First total synthesis of xestobergsterol A and active structural analogues of the xestobergsterols Tetrahedron. 57: 1449-1481. DOI: 10.1016/S0040-4020(00)01086-3 |
0.365 |
|
| 2000 |
Jung ME, Huang A. Use of optically active cyclic N,N-dialkyl aminals in asymmetric induction. Organic Letters. 2: 2659-61. PMID 10990421 DOI: 10.1021/Ol0001517 |
0.58 |
|
| 2000 |
Jung ME, Huang A, Johnson TW. 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. Organic Letters. 2: 1835-1837. PMID 10891170 DOI: 10.1021/Ol000104E |
0.625 |
|
| 2000 |
Jung ME, Marquez R. Efficient synthesis of the C(1)-C(11) fragment of the tedanolides. The nonaldol aldol process in synthesis. Organic Letters. 2: 1669-72. PMID 10880197 DOI: 10.1021/Ol005675L |
0.435 |
|
| 2000 |
Rhee H, Yoon D, Jung ME. Efficient synthesis of carbocyclic nucleoside, (+/-)-homocarbovir via pi-allylpalladium complex formation from the allyl-N,N-ditosylimide substrate. Nucleosides, Nucleotides & Nucleic Acids. 19: 619-28. PMID 10843497 DOI: 10.1080/15257770008035012 |
0.423 |
|
| 2000 |
Jung ME, Johnson TW. First total synthesis of xestobergsterol A and active structural analogues of the xestobergsterols. Organic Letters. 1: 1671-4. PMID 10836028 DOI: 10.1021/Ol991057X |
0.445 |
|
| 2000 |
Jung ME, Xu Y. Efficient synthesis of 2-deoxy L-ribose from L-arabinose: mechanistic information on the 1,2-acyloxy shift in alkyl radicals. Organic Letters. 1: 1517-9. PMID 10836018 DOI: 10.1021/Ol990838V |
0.315 |
|
| 2000 |
Jung ME, Lee WS, Sun D. Synthesis of four diastereomeric 3,5-dialkoxy-2,4-dimethylalkanals by a simple extension of the non-aldol aldol process to bis(propionates). Organic Letters. 1: 307-9. PMID 10822567 DOI: 10.1021/Ol990619+ |
0.456 |
|
| 2000 |
Jung ME, Fahr BT. Novel base-induced [1,2]-acyl shift of allylic esters of cyclopropanecarboxylic acids. The Journal of Organic Chemistry. 65: 2239-42. PMID 10774055 DOI: 10.1021/Jo991706I |
0.339 |
|
| 2000 |
Jung ME, Lee CP. Use of the non-aldol aldol process in the synthesis of the C1-C11 fragment of the tedanolides: Use of lactol ethers in place of tetrahydrofurans Tetrahedron Letters. 41: 9719-9723. DOI: 10.1016/S0040-4039(00)01726-3 |
0.382 |
|
| 2000 |
Jung ME, Toyota A. Efficient synthesis of several methylene-expanded oxetanocin nucleoside analogues Tetrahedron Letters. 41: 3577-3581. DOI: 10.1016/S0040-4039(00)00467-6 |
0.4 |
|
| 1999 |
Jung ME, Lazarova TI. New Efficient Method for the Total Synthesis of (S,S)-Isodityrosine from Natural Amino Acids. The Journal of Organic Chemistry. 64: 2976-2977. PMID 11674381 DOI: 10.1021/Jo9902751 |
0.785 |
|
| 1999 |
Jung ME, Pontillo J. Facile preparation of allenic hydroxyketones via rearrangement of propargylic alcohols. Organic Letters. 1: 367-9. PMID 10822577 |
0.74 |
|
| 1999 |
Jung ME, Yang EC, Vu BT, Kiankarimi M, Spyrou E, Kaunitz J. Glycosylation of fluoroquinolones through direct and oxygenated polymethylene linkages as a sugar-mediated active transport system for antimicrobials. Journal of Medicinal Chemistry. 42: 3899-909. PMID 10508438 DOI: 10.1021/Jm990015B |
0.655 |
|
| 1999 |
Jung ME, Nichols CJ, Kretschik O, Xu Y. Synthesis and testing of new modified nucleosides. Nucleosides & Nucleotides. 18: 541-6. PMID 10432645 DOI: 10.1080/15257779908041490 |
0.327 |
|
| 1999 |
Jung ME, Mengel W, Newton TW. A Short, Convenient Synthesis of 2-ArylglycidatesviaAryl-Grignard Addition to an α-Bromopyruvate Synthetic Communications. 29: 3659-3666. DOI: 10.1080/00397919908086003 |
0.364 |
|
| 1999 |
Jung ME. New Gem- and Vic-Disubstituent Effects on Cyclizations Synlett. 1999: 843-846. DOI: 10.1055/S-1999-3086 |
0.301 |
|
| 1999 |
Jung ME, Johnson TW. Unusual Cyclization Products Derived from Photolysis of Breslow's Steroidal Benzophenone Esters The Journal of Organic Chemistry. 64: 7651-7653. DOI: 10.1021/Jo990800W |
0.368 |
|
| 1999 |
Jung ME, Karama U, Marquez R. Conversion Of Homoallylic Alcohols With Alkene Protection To The Corresponding Methyl Ketones Journal of Organic Chemistry. 64: 663-665. DOI: 10.1021/Jo9817725 |
0.319 |
|
| 1999 |
Jung ME, Sun D. Stereoselective production of β-amino alcohols and β-thioacyl alcohols via an application of the non-aldol aldol process Tetrahedron Letters. 40: 8343-8346. DOI: 10.1016/S0040-4039(99)01786-4 |
0.331 |
|
| 1999 |
Jung ME, Karama U. Highly diastereoselective Markovnikov hydration of 3,4-dialkoxy-1-alkenes and 4,5-dialkoxy-2-alkenes via a hydroboration-oxidation process Tetrahedron Letters. 40: 7907-7910. DOI: 10.1016/S0040-4039(99)01496-3 |
0.327 |
|
| 1999 |
Jung ME, MacDougall JM. First enantioselective total synthesis of the endogenous natriuretic agent LLU-α Tetrahedron Letters. 40: 6339-6342. DOI: 10.1016/S0040-4039(99)01204-6 |
0.401 |
|
| 1999 |
Jung ME, Marquez R. Rearrangement of epoxides in non-aldol aldol process: Allylic vs. Tertiary and secondary carbocationic centers Tetrahedron Letters. 40: 3129-3132. DOI: 10.1016/S0040-4039(99)00458-X |
0.48 |
|
| 1999 |
Jung ME, Marquez R, Houk K. The influence of geminal disubstitution on efficiencies of 4-exo-trig radical cyclizations Tetrahedron Letters. 40: 2661-2664. DOI: 10.1016/S0040-4039(99)00292-0 |
0.416 |
|
| 1998 |
Jung ME, Castro C, Khan SI. Novel Lewis Acid-Catalyzed Rearrangement of a Sugar-Base Hybrid to Afford an Anhydronucleoside Nucleosides and Nucleotides. 17: 2383-2387. DOI: 10.1080/07328319808004325 |
0.371 |
|
| 1998 |
Jung ME, Kiankarimi M. Synthesis of Methylene-Expanded 2‘,3‘-Dideoxyribonucleosides The Journal of Organic Chemistry. 63: 8133-8144. DOI: 10.1021/Jo980436L |
0.407 |
|
| 1998 |
Jung ME, Fahr BT, D'Amico DC. Total Syntheses of the Cytotoxic Marine Natural Product, Aplysiapyranoid C1 The Journal of Organic Chemistry. 63: 2982-2987. DOI: 10.1021/Jo972228J |
0.435 |
|
| 1998 |
Jung ME, Kretschik O. Enantiospecific Total Synthesis ofl-2‘,3‘-Dideoxyisonucleosides via Regioselective Opening of Optically ActiveC2-Symmetric 1,4-Pentadiene Bis-epoxide1 The Journal of Organic Chemistry. 63: 2975-2981. DOI: 10.1021/Jo9721655 |
0.457 |
|
| 1998 |
Jung ME, Kiankarimi M. Substituent Effects in the Intramolecular Diels−Alder Reaction of 6-Furylhexenoates The Journal of Organic Chemistry. 63: 2968-2974. DOI: 10.1021/Jo9721554 |
0.48 |
|
| 1998 |
Jung ME, Nichols CJ. Synthesis of Methylene-Expanded Oxetanocin Isonucleosides in Both Enantiomeric Forms1 The Journal of Organic Chemistry. 63: 347-355. DOI: 10.1021/Jo971890C |
0.39 |
|
| 1998 |
Jung ME, Nichols CJ. A de novo synthesis of ethyl 2-deoxy-l-ribosides Tetrahedron Letters. 39: 4615-4618. DOI: 10.1016/S0040-4039(98)00852-1 |
0.356 |
|
| 1997 |
Jung ME, Parker MH. Synthesis of Several Naturally Occurring Polyhalogenated Monoterpenes of the Halomon Class(1). The Journal of Organic Chemistry. 62: 7094-7095. PMID 11671809 DOI: 10.1021/Jo971371+ |
0.552 |
|
| 1997 |
Jung ME, Angelica S, D'Amico DC. An Intramolecular Prins Double Cyclization Catalyzed by Silyl Triflates1 The Journal of Organic Chemistry. 62: 9182-9187. DOI: 10.1021/Jo971337V |
0.395 |
|
| 1997 |
Jung ME, Rayle HL. Generation of [5.5.n] Tricyclic Ring Systems by Radical-Promoted Inter- and Intramolecular [3 + 2] Cycloadditions The Journal of Organic Chemistry. 62: 4601-4609. DOI: 10.1021/Jo9706133 |
0.371 |
|
| 1997 |
Jung ME, Lazarova TI. Efficient Synthesis of Selectively Protectedl-Dopa Derivatives froml-Tyrosine via Reimer−Tiemann and Dakin Reactions The Journal of Organic Chemistry. 62: 1553-1555. DOI: 10.1021/Jo962099R |
0.455 |
|
| 1997 |
Giessner-Prettre C, Hückel S, Maddaluno J, Jung ME. Molecular Mechanics/Continuum Reaction Field/Quantum Mechanics Study of the Intramolecular Diels−Alder Reaction of 2-Furfuryl Derivatives Journal of Organic Chemistry. 62: 1439-1448. DOI: 10.1021/Jo9609586 |
0.359 |
|
| 1997 |
Jung ME, Johnson TW. Synthesis of 7-Deoxyxestobergsterol A, a Novel Pentacyclic Steroid of the Xestobergsterol Class1 Journal of the American Chemical Society. 119: 12412-12413. DOI: 10.1021/Ja9733189 |
0.332 |
|
| 1997 |
Jung ME, D'Amico DC. Stereospecific Formation of Optically Active 5-Alkyl-4-methyl-3-[(trialkylsilyl)oxy]-2-([(trialkylsilyl)oxy]- methyl)tetrahydrofurans via Diastereoselective Epoxidation and Rearrangement of 5-[(Trialkylsilyl)oxy]-2-alken-1-ols1 Journal of the American Chemical Society. 119: 12150-12158. DOI: 10.1021/Ja972507O |
0.379 |
|
| 1997 |
Jung ME, Marquez R. Gem-disubstituent effects in small ring formation: Novel ketal ring size effect Tetrahedron Letters. 38: 6521-6524. DOI: 10.1016/S0040-4039(97)01519-0 |
0.407 |
|
| 1997 |
Jung ME, Anderson KL. Stereospecific rearrangements of optically active 2-aryl-3-ethenyloxiranes to give optically active β-ethenylbenzeneethanols: Benzyl vs. allyl cations and an efficient synthesis of (s)-ibuprofen Tetrahedron Letters. 38: 2605-2608. DOI: 10.1016/S0040-4039(97)00425-5 |
0.369 |
|
| 1997 |
Jung ME, Starkey LS. Total synthesis of (S,S)-isodityrosine Tetrahedron. 53: 8815-8824. DOI: 10.1016/S0040-4020(97)90393-8 |
0.427 |
|
| 1996 |
Jung ME, Nichols CJ. A Novel Tandem [1,2]-Brook/Retro-[1,6]-Brook Rearrangement of a 1-(Trimethylsilyl)-2,4-pentadien-1-ol Anion. The Journal of Organic Chemistry. 61: 9065-9067. PMID 11667902 DOI: 10.1021/Jo961265S |
0.337 |
|
| 1996 |
Jung ME, Vu BT. Complete Diastereocontrol in Intramolecular 1,3-Dipolar Cycloadditions of 2-Substituted 5-Hexenyl and 5-Heptenyl Nitrones: Application to the Synthesis of the beta-Lactam Antibiotic 1beta-Methylthienamycin. The Journal of Organic Chemistry. 61: 4427-4433. PMID 11667348 DOI: 10.1021/Jo952254M |
0.709 |
|
| 1996 |
Jung ME, Nichols CJ. Highly stereoselective synthesis of trans,trans-4-aryl-2,3-oxetanedimethanols: Preparation of oxetanocin a analogues Tetrahedron Letters. 37: 7667-7670. DOI: 10.1016/0040-4039(96)01720-0 |
0.436 |
|
| 1996 |
McGee DPC, Sebesta DP, O'Rourke SS, Martinez RL, Jung ME, Pieken WA. Novel nucleosides via intramolecular functionalization of 2,2'-anhydrouridine derivatives Tetrahedron Letters. 37: 1995-1998. DOI: 10.1016/0040-4039(96)00227-4 |
0.454 |
|
| 1996 |
Jung ME, Vu BT. Substituent effects on intramolecular dipolar cycloadditions: The gem-dicarboalkoxy effect Tetrahedron Letters. 37: 451-454. DOI: 10.1016/0040-4039(95)02196-5 |
0.701 |
|
| 1996 |
Jung ME, Lazarova TI. Preparation of (phenylsulfinyl)phenols from aryl phenylsulfinates: ‘Thia-Fries rearrangement’ Tetrahedron Letters. 37: 7-8. DOI: 10.1016/0040-4039(95)02068-3 |
0.446 |
|
| 1996 |
Jung ME, Cho YM, Jung YH. Facile synthesis of optically active 2-hydroxymethyl-4-methylene-cyclohexanol. De novo synthesis of dideoxycarbocyclic sugars Tetrahedron Letters. 37: 3-6. DOI: 10.1016/0040-4039(95)02067-5 |
0.421 |
|
| 1995 |
Jung ME, Jung YH. Efficient Enantioselective Synthesis of (2S,3R) Methyl β-Hydroxytyrosinate from Achiral Starting Materials Synlett. 1995: 563-564. DOI: 10.1055/S-1995-5292 |
0.331 |
|
| 1995 |
Jung ME, D'Amico DC. Stereospecific Rearrangement of Optically Active Tertiary Allylic Epoxides To Give Optically Active Quaternary Aldehydes: Synthesis of .alpha.-Alkyl Amino Aldehydes and Acids Journal of the American Chemical Society. 117: 7379-7388. DOI: 10.1021/Ja00133A011 |
0.338 |
|
| 1995 |
Jung ME, Starkey LS. New preparation of o-aryloxyphenols via cyclohexenone oxides Tetrahedron Letters. 36: 7363-7366. DOI: 10.1016/0040-4039(95)01657-0 |
0.323 |
|
| 1994 |
Jung ME, Rayle HL. An Improved Synthesis of 4-Methylene-2-cyclohexen-1-one Synthetic Communications. 24: 197-203. DOI: 10.1080/00397919408013819 |
0.418 |
|
| 1994 |
Jung ME, Rhee H. .pi.-Allylpalladium Formation from Allylic Amines via N,N-Ditosylimides and N-Tosylamides: Efficient Synthesis of the Antiviral Agent Carbovir The Journal of Organic Chemistry. 59: 4719-4720. DOI: 10.1021/Jo00096A006 |
0.342 |
|
| 1994 |
Harrington PM, Jung ME. Stereoselective bromination of β-ribofuranosyl amide. Enantioselective synthesis of (+)-hydantocidin Tetrahedron Letters. 35: 5145-5148. DOI: 10.1016/S0040-4039(00)77049-3 |
0.347 |
|
| 1994 |
Jung ME, Gardiner JM. Asymmetric synthesis of carbohydrates: Synthesis of 2-deoxy-D- and 2-deoxy-L-xylofuranosides from a simple achiral precursor Tetrahedron Letters. 35: 6755-6758. DOI: 10.1016/S0040-4039(00)73487-3 |
0.591 |
|
| 1993 |
Nagao Y, Takahashi M, Abe Y, Misono T, Jung ME. Synthesis of 1,1-Dialkoxy Derivatives of 2,5-Diphenylsilacyclopent-3-ene and 2,5-Diphenylsilacyclopentane Bulletin of the Chemical Society of Japan. 66: 2294-2297. DOI: 10.1246/Bcsj.66.2294 |
0.412 |
|
| 1993 |
Jung ME, Sledeski AW. Efficient total synthesis of racemic and optically active cyclobut-A and simple analogues Journal of the Chemical Society, Chemical Communications. 589-591. DOI: 10.1039/C39930000589 |
0.389 |
|
| 1993 |
Jung ME, Castro C. New approach to the synthesis of .beta.-2'-deoxyribonucleosides: intramolecular Vorbrueggen coupling The Journal of Organic Chemistry. 58: 807-808. DOI: 10.1021/Jo00056A004 |
0.34 |
|
| 1993 |
Jung ME, D'Amico DC. Enantiospecific synthesis of all four diastereomers of 2-methyl-3-[(trialkylsilyl)oxy]alkanals: facile preparation of aldols by non-aldol chemistry Journal of the American Chemical Society. 115: 12208-12209. DOI: 10.1021/Ja00078A087 |
0.404 |
|
| 1993 |
Jung ME, Siedem CS. Efficient synthesis of a hexasubstituted aromatic ring via an intramolecular Michael-aldol process: preparation of a late tricyclic intermediate for the synthesis of pseudopterosin A Journal of the American Chemical Society. 115: 3822-3823. DOI: 10.1021/Ja00062A077 |
0.453 |
|
| 1993 |
Jung ME, Choe S. Stereospecific intramolecular formyl transfer via radical cyclization-fragmentation: Preparation of alkyl 2-deoxy-2α-formylglucopyranosides and similar compounds Tetrahedron Letters. 34: 6247-6250. DOI: 10.1016/S0040-4039(00)73722-1 |
0.42 |
|
| 1993 |
Jung ME, Zimmerman CN, Lowen GT, Khan SI. Diastereocontrol in intermolecular diels-alder reactions of allenic lactones: Synthetic approach to the plaunols Tetrahedron Letters. 34: 4453-4456. DOI: 10.1016/0040-4039(93)88057-P |
0.433 |
|
| 1993 |
Jung ME, Rhee H. New efficient method for the synthesis of the antiviral agent carbovir Tetrahedron Letters. 34: 4449-4452. DOI: 10.1016/0040-4039(93)88056-O |
0.343 |
|
| 1992 |
Jung ME, Zeng L, Peng T, Zeng H, Le Y, Su J. Total synthesis of Bao Gong Teng A, a natural antiglaucoma compound The Journal of Organic Chemistry. 57: 3528-3530. DOI: 10.1021/Jo00039A005 |
0.424 |
|
| 1992 |
Jung ME, Trifunovich ID. Efficient synthesis of 2′,3′-dideoxynucleosides and 2′,3′-dideoxy C-nucleosides from D-glucosamine Tetrahedron Letters. 33: 2921-2924. DOI: 10.1016/S0040-4039(00)79561-X |
0.333 |
|
| 1992 |
Jung ME, Gardiner JM. Synthesis of antiviral nucleosides from crotonaldehyde. Part 3.1,2 total synthesis of didehydrodideoxythymidine (d4T) Tetrahedron Letters. 33: 3841-3844. DOI: 10.1016/S0040-4039(00)74799-X |
0.623 |
|
| 1992 |
Jung ME, Trifunovich ID, Lensen N. Easy preparation of a cyclobutanone ketal via a radical cyclization. The gem-dialkoxy effect Tetrahedron Letters. 33: 6719-6722. DOI: 10.1016/S0040-4039(00)61759-8 |
0.418 |
|
| 1991 |
Jung ME, Choi YM. New synthesis of 2-azetines and 1-azabutadienes and the use of the latter in Diels-Alder reactions: total synthesis of (.+-.)-.delta.-coniceine The Journal of Organic Chemistry. 56: 6729-6730. DOI: 10.1021/JO00024A001 |
0.366 |
|
| 1991 |
Jung ME, Gardiner JM. Synthetic approaches to 3'-azido-3'-deoxythymidine and other modified nucleosides The Journal of Organic Chemistry. 56: 2614-2615. DOI: 10.1021/Jo00008A006 |
0.602 |
|
| 1991 |
Jung ME, Lew W. Efficient total synthesis of the cytotoxic halogenated monoterpene aplysiapyranoid D The Journal of Organic Chemistry. 56: 1347-1349. DOI: 10.1021/Jo00004A001 |
0.327 |
|
| 1991 |
Jung ME, Zimmerman CN. New synthesis of methyl 1,3-butadiene-2-carboxylate by the cheletropic extrusion of carbon monoxide from 3-carbomethoxy-3,4-pentadienal and a study of its dimerization to give dimethyl mikanecate (dimethyl 4-ethenyl-1-cyclohexene-1,4-dicarboxylate) Journal of the American Chemical Society. 113: 7813-7814. DOI: 10.1021/Ja00020A082 |
0.344 |
|
| 1991 |
Jung ME, Gervay J. gem-Dialkyl effect in the intramolecular Diels-Alder reaction of 2-furfuryl methyl fumarates: the reactive rotamer effect, the enthalpic basis for acceleration, and evidence for a polar transition state Journal of the American Chemical Society. 113: 224-232. DOI: 10.1021/Ja00001A032 |
0.398 |
|
| 1991 |
Jung ME, Castro C, Gardiner JM. Rapid synthesis of 2′,3′-dideoxycytidine (ddC) from a simple achiral precursor Tetrahedron Letters. 32: 5717-5720. DOI: 10.1016/S0040-4039(00)93538-X |
0.614 |
|
| 1991 |
Jung ME, Hagiwara A. New alkene-forming reaction: phenanthrenes from 2-(2-formylphenyl)benzaldehyde bis-tosylhydrazone decomposition Tetrahedron Letters. 32: 3025-3028. DOI: 10.1016/0040-4039(91)80677-X |
0.414 |
|
| 1990 |
Jung ME, Trifunovich ID, Gardiner JM, Clevenger GL. Preparation of modified nucleosides from glucosamine: Rapid and efficient formal total synthesis of several 2′-deoxy C-nucleosides Journal of the Chemical Society, Chemical Communications. 84-85. DOI: 10.1039/C39900000084 |
0.577 |
|
| 1990 |
Jung ME, Lew W. Diastereoselective organocuprate addition to homochiral ketals of 3-acetylcyclopent-2-en-1-one Tetrahedron Letters. 31: 623-626. DOI: 10.1016/S0040-4039(00)94584-2 |
0.343 |
|
| 1990 |
JUNG ME. ChemInform Abstract: Substituent and Solvent Effects in Intramolecular Diels-Alder Reactions Cheminform. 21. DOI: 10.1002/CHIN.199038363 |
0.332 |
|
| 1989 |
Jung ME, Gervay J. Solvent effects in intramolecular Diels-Alder reactions of 2-furfuryl methyl fumarates: evidence for a polar transition state Journal of the American Chemical Society. 111: 5469-5470. DOI: 10.1021/Ja00196A065 |
0.352 |
|
| 1989 |
Jung ME, Jachiet D, Rohloff JC. Facile chemical synthesis of S,S-isodityrosine, a naturally-occurring cross-linking amino acid Tetrahedron Letters. 30: 4211-4214. DOI: 10.1016/S0040-4039(01)80692-4 |
0.346 |
|
| 1989 |
Jung ME, Kaas SM. Facile synthesis of a substituted bicyclo[4.2.1]nonane via an anionic [1,3]-sigmatropic shift: Use of long range 2D HETCOR and difference NOE in structure determination Tetrahedron Letters. 30: 641-644. DOI: 10.1016/S0040-4039(01)80270-7 |
0.378 |
|
| 1989 |
Jung ME, Vaccaro WD, Buszek KR. Asymmetric diels-alder reactions of chiral alkoxy iminium salts Tetrahedron Letters. 30: 1893-1896. DOI: 10.1016/S0040-4039(00)99606-0 |
0.381 |
|
| 1989 |
Jung ME, Jung YH. Rapid synthesis of β-hydroxy-α-amino acids, such as L-threonine, β-hydroxyphenylalanine, and β-hydroxyleucine, via an application of the sharpless asymmetric epoxidation Tetrahedron Letters. 30: 6637-6640. DOI: 10.1016/S0040-4039(00)70638-1 |
0.327 |
|
| 1989 |
JUNG ME, VACCARO WD, BUSZEK KR. ChemInform Abstract: Asymmetric Diels-Alder Reactions of Chiral Alkoxyiminium Salts. Cheminform. 20. DOI: 10.1002/CHIN.198941135 |
0.323 |
|
| 1988 |
Jung ME, Buszek KR. The stereochemistry of addition of trialkylammonium and pyridinium tetrafluoroborate salts to activated acetylenes. Preparation of novel dienophiles for diels-alder reactions Journal of the American Chemical Society. 110: 3965-3969. DOI: 10.1021/Ja00220A039 |
0.457 |
|
| 1988 |
Jung ME, Gervay J. Studies on the effects of substituents on rate enhancements in intramolecular diels-alder reactions: Reasons for the gem-dimethyl effect Tetrahedron Letters. 29: 2429-2432. DOI: 10.1016/S0040-4039(00)87899-5 |
0.377 |
|
| 1988 |
Jung ME, Jung YH. Total synthesis of the aglycone of the 8-methyl benzonaphthopyrone antibiotics, gilvocarcin M, virenomycin M, and albacarcin M Tetrahedron Letters. 29: 2517-2520. DOI: 10.1016/S0040-4039(00)86100-6 |
0.329 |
|
| 1988 |
Jung ME, Truc VC. Intramolecular diels-alder cycloadditions of substituted furfuryl E-2-(phenylsulfonyl)acrylates Tetrahedron Letters. 29: 6059-6062. DOI: 10.1016/S0040-4039(00)82264-9 |
0.438 |
|
| 1988 |
JUNG ME, BUSZEK KR. ChemInform Abstract: The Stereochemistry of Addition of Trialkylammonium and Pyridinium Tetrafluoroborate Salts to Activated Acetylenes. Preparation of Novel Dienophiles for Diels-Alder Reactions. Cheminform. 19. DOI: 10.1002/CHIN.198840077 |
0.343 |
|
| 1987 |
Jung ME, Grove DD. Nitroacetylene equivalents. Preparation and cycloadditions of 2-phenylsulphinyl-1-nitroalkenes Journal of the Chemical Society, Chemical Communications. 753-755. DOI: 10.1039/C39870000753 |
0.463 |
|
| 1987 |
Jung ME, Usui Y, Vu CT. Rapid and efficient synthesis of a fully functionalized synthon for the bottom half of the antiparasitic agent, ivermectin Tetrahedron Letters. 28: 5977-5980. DOI: 10.1016/S0040-4039(00)96841-2 |
0.411 |
|
| 1987 |
JUNG ME, HAGENAH JA. ChemInform Abstract: Preparation and Cycloaddition of Functionalized 4,6-Dialkylpyrone-5- carboxylates. Synthesis of Bicyclic Lactones and Substituted Benzoates. Cheminform. 18. DOI: 10.1002/CHIN.198725146 |
0.344 |
|
| 1987 |
JUNG ME, LOWEN GT. ChemInform Abstract: A Direct Synthesis of trans-2-Arylbenzocyclobutenol, a Potential Intermediate for Podophyllotoxin Synthesis: Use of LDA for Benzyne Formation and Trapping. Cheminform. 18. DOI: 10.1002/CHIN.198714208 |
0.324 |
|
| 1986 |
Jung ME, Street LJ, Usui Y. Chemoselective cycloadditions of 3,4-dialkoxyfurans and alkyl coumalates. Novel loss of aromaticity of two nonbenzenoid aromatic rings in a mild thermal process Journal of the American Chemical Society. 108: 6810-6811. DOI: 10.1021/Ja00281A062 |
0.348 |
|
| 1986 |
Jung ME, Buszek KR. Alkenylimmonium salts as dienophiles in Diels-Alder cycloadditions with high reactivity and stereoselectivity Tetrahedron Letters. 27: 6165-6168. DOI: 10.1016/S0040-4039(00)85423-4 |
0.432 |
|
| 1986 |
Jung ME, Lowen GT. A direct synthesis of 2-arylbenzocyclobutenol, a potential intermediate for podophyllotoxin synthesis: Use of lda for benzyne formation and trapping Tetrahedron Letters. 27: 5319-5322. DOI: 10.1016/S0040-4039(00)85200-4 |
0.43 |
|
| 1986 |
JUNG ME, BUSZEK KR. ChemInform Abstract: Alkenyltrialkylammonium Salts as Dienophiles in Diels-Alder Reactions: Preparation, Cycloadditions and Further Reactions. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198620086 |
0.433 |
|
| 1985 |
Jung ME, Buszek KR. Alkenyltrialkylammonium salts as dienophiles in Diels-Alder reactions: Preparation, cycloadditions, and further reactions. β-(Dimethylamino)acrylonitrile equivalent in cycloadditions Journal of Organic Chemistry. 50: 5440-5441. DOI: 10.1021/Jo00225A106 |
0.431 |
|
| 1985 |
Jung ME, Rohloff JC. Organic chemistry of L-tyrosine. 1. General synthesis of chiral piperazines from amino acids Journal of Organic Chemistry. 50: 4909-4913. DOI: 10.1021/Jo00224A051 |
0.346 |
|
| 1985 |
Jung ME, Lam PYS, Mansuri MM, Speltz LM. Stereoselective synthesis of an analog of podophyllotoxin by an intramolecular Diels-Alder reaction The Journal of Organic Chemistry. 50: 1087-1105. DOI: 10.1021/Jo00207A034 |
0.498 |
|
| 1985 |
JUNG ME, LAM PY, MANSURI MM, SPELTZ LM. ChemInform Abstract: STEREOSELECTIVE SYNTHESIS OF AN ANALOG OF PODOPHYLLOTOXIN BY AN INTRAMOLECULAR DIELS-ALDER REACTION Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198535339 |
0.403 |
|
| 1985 |
JUNG ME, STREET LJ. ChemInform Abstract: SYNTHETIC STUDIES ON THE AVERMECTINS: SUBSTITUENT EFFECTS ON INTRAMOLECULAR DIELS-ALDER REACTIONS OF N-FURFURYLACRYLAMIDES AND FURTHER REACTIONS OF THE CYCLOADDUCTS Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198517091 |
0.316 |
|
| 1985 |
JUNG ME, LOWE JAI, LYSTER MA, NODE M, PFLUGER RW, BROWN RW. ChemInform Abstract: REGIOSPECIFIC SYNTHESIS OF MONO- AND BICYCLIC 6-ALKOXY-2-PYRONES AND THEIR USE IN THE PREPARATION OF SUBSTITUTED AROMATICS, ANTHRAQUINONES, AND TETRACYCLIC INTERMEDIATES FOR 11-DEOXYANTHRACYCLINE SYNTHESIS Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198513168 |
0.369 |
|
| 1984 |
Jung ME, Rohloff JC. Intramolecular Diels–Alder chemistry of pyrroles Journal of the Chemical Society, Chemical Communications. 630-632. DOI: 10.1039/C39840000630 |
0.445 |
|
| 1984 |
Jung ME, Light LA. Stereospecific synthesis of substituted cis-hydrindan-5-one and their regiospecific enolization and functionalization: synthetic intermediates for reserpine Journal of the American Chemical Society. 106: 7614-7618. DOI: 10.1021/Ja00336A049 |
0.397 |
|
| 1984 |
Jung ME, Halweg KM. Stereoselectivity in intramolecular diels-alder reactions; a short total synthesis of (±)-estrone Tetrahedron Letters. 25: 2121-2124. DOI: 10.1016/S0040-4039(01)81177-1 |
0.376 |
|
| 1984 |
Jung ME, Lowe JA, Lyster MA, Node M, Pfluger RW, Brown RW. Regiospecific synthesis of mono- and bicyclic 6-alkoxy-2-pyrones and their use in the preparation of substituted aromatics, anthraquinones, and tetracyclic intermediates for 11-deoxyanthracycline synthesis Tetrahedron. 40: 4751-4766. DOI: 10.1016/S0040-4020(01)91537-6 |
0.473 |
|
| 1984 |
Jung ME, Brown RW, Hagenah JA, Strouse CE. Cyloadditions of benzopyrones: Rapid access to bicyclic AB-ring analogues of anthracyclines Tetrahedron Letters. 25: 3659-3662. DOI: 10.1016/0040-4039(84)80098-2 |
0.392 |
|
| 1984 |
Jung ME, Street LJ. Synthetic studies on the avermectins: substituent effects on intramolecular Diels-Alder reactions of N-furfurylacrylamides and further reactions of the cycloadducts Journal of the American Chemical Society. 106: 8327-8329. DOI: 10.1002/Chin.198517091 |
0.422 |
|
| 1984 |
JUNG ME, ROHLOFF JC. ChemInform Abstract: INTRAMOLECULAR DIELS-ALDER CHEMISTRY OF PYRROLES Chemischer Informationsdienst. 15. DOI: 10.1002/Chin.198439087 |
0.437 |
|
| 1984 |
JUNG ME, HALWEG KM. ChemInform Abstract: STEREOSELECTIVITY IN INTRAMOLECULAR DIELS-ALDER REACTIONS; A SHORT TOTAL SYNTHESIS OF (.+-.)-ESTRONE Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198436298 |
0.39 |
|
| 1983 |
Jung ME, Lewis PK. Addition of Organocuprates to α-Iodoalkyl Trimethylsilyl Ethers Formed from Aldehydes and Trimethylsilyl Iodide Synthetic Communications. 13: 213-218. DOI: 10.1080/00397918308065991 |
0.409 |
|
| 1983 |
Jung ME, Hagenah JA, Long-Mei Z. Simple, stereospecific preparation of -3-iodoacrylic acid from propiolic acid and methylmagnesium iodide Tetrahedron Letters. 24: 3973-3974. DOI: 10.1016/S0040-4039(00)88239-8 |
0.327 |
|
| 1983 |
Jung ME, Hatfield GL. Facile synthesis of (3as)-1,3a-dimethyl-2,3,3a,5,6,7- hyxahydroinden-4(5h)-one, an intermediate for steroid synthesis Tetrahedron Letters. 24: 3175-3178. DOI: 10.1016/S0040-4039(00)88128-9 |
0.332 |
|
| 1983 |
Jung ME, Hatfield GL. Synthesis of syn-7-benzyloxy-4-methylbicyclo[2.2.1]hept-5-en-2-one, an intermediate for the synthesis of steroids and tricothecanes; tandem anionic [1,3]–[3,3] sigmatropic rearrangement Tetrahedron Letters. 24: 2931-2934. DOI: 10.1016/S0040-4039(00)88061-2 |
0.434 |
|
| 1983 |
Jung ME, Long-Mei Z. Reactions of oximes with trimethylsilyl iodide: dehydration and beckmann rearrangement Tetrahedron Letters. 24: 4533-4534. DOI: 10.1016/S0040-4039(00)85947-X |
0.475 |
|
| 1983 |
JUNG ME, HATFIELD GL. ChemInform Abstract: SYNTHESIS OF SYN-7-BENZYLOXY-4-METHYLBICYCLO(2.2.1)HEPT-5-EN-2-ONE, AN INTERMEDIATE FOR THE SYNTHESIS OF STEROIDS AND TRICOTHECANES; TANDEM ANIONIC (1,3)-(3,3) SIGMATROPIC REARRANGEMENT Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198344189 |
0.344 |
|
| 1982 |
Jung ME, Node M, Pfluger RW, Lyster MA, Lowe JA. Regiospecific synthesis of bicyclic 6-alkoxy-2-pyrones and their use in the production of tetracyclic intermediates for 11-deoxyanthracycline synthesis The Journal of Organic Chemistry. 47: 1150-1152. DOI: 10.1021/Jo00345A058 |
0.426 |
|
| 1982 |
Jung ME, Light LA. Intramolecular Diels-Alder cycloadditions of perchloro(allyloxy)- and perchlorobis(allyloxy)cyclopentadienes The Journal of Organic Chemistry. 47: 1084-1090. DOI: 10.1021/Jo00345A038 |
0.477 |
|
| 1982 |
Jung ME, Shishido K, Davis LH. Simple syntheses of diethyl oxomalonate and alkyl glyoxylates The Journal of Organic Chemistry. 47: 891-892. DOI: 10.1021/Jo00344A028 |
0.438 |
|
| 1982 |
Jung ME, Hatfield GL. Novel oxidative rearrangement of β,γ-unsaturated ketone hydrazones on iodination in base Tetrahedron Letters. 23: 3991-3994. DOI: 10.1016/S0040-4039(00)88677-3 |
0.371 |
|
| 1982 |
Jung ME, Light LA. Preparation of iodoallylic alcohols via hydrostannylation: spectroscopic proof of structures Tetrahedron Letters. 23: 3851-3854. DOI: 10.1016/S0040-4039(00)87725-4 |
0.304 |
|
| 1982 |
JUNG ME, BLUM RB. ChemInform Abstract: PHOTOCHEMICAL TRANSFORMATIONS OF METHOXYPHTHALALDEHYDIC ESTERS: SYNTHESIS OF METHYL 6-METHOXYPHTHALALDEHYDATE FROM THE 3-METHOXY ISOMER Chemischer Informationsdienst. 13. DOI: 10.1002/Chin.198204200 |
0.368 |
|
| 1982 |
JUNG ME, BROWN RW. ChemInform Abstract: REGIOSPECIFIC FRIEDEL-CRAFTS ACYLATION OF 6-ALKOXY-2-PYRONES: PREPARATION OF SUBSTITUTED AROMATICS AND ANTHRAQUINONES Chemischer Informationsdienst. 13. DOI: 10.1002/chin.198201187 |
0.326 |
|
| 1981 |
Jung ME, Blum RB. Photochemical transformations of methoxyphthalaldehydic esters: synthesis of methyl 6-methoxyphthalaldehydate from the 3-methoxy-isomer Journal of the Chemical Society, Chemical Communications. 962-963. DOI: 10.1039/C39810000962 |
0.365 |
|
| 1981 |
Jung ME, McCombs CA, Takeda Y, Pan Y. Use of silyloxydienes in synthesis. Total syntheses of the sesquiterpene (.+-.)-seychellene Journal of the American Chemical Society. 103: 6677-6685. DOI: 10.1021/Ja00412A024 |
0.391 |
|
| 1981 |
Jung ME, Halweg KM. Intramolecular Lewis-acid promoted (2+2) cycloadditions: An efficient total synthesis of (±)-coronafacic acid via an internal Diels-Alder reaction. Tetrahedron Letters. 22: 2735-2738. DOI: 10.1016/S0040-4039(01)90538-6 |
0.459 |
|
| 1981 |
Jung ME, Shishido K, Light L, Davis L. Preparation of di- and triacylimines and their use in the synthesis of nitrogen heterocycles Tetrahedron Letters. 22: 4607-4610. DOI: 10.1016/S0040-4039(01)82993-2 |
0.508 |
|
| 1981 |
Jung ME, Halweg KM. Simple regioselective synthesis of -7a-methylhydrind-4-en-1-one, a key intermediate for steroid total synthesis Tetrahedron Letters. 22: 3929-3932. DOI: 10.1016/S0040-4039(01)82029-3 |
0.395 |
|
| 1981 |
Jung ME, Brown RW. Regiospecific friedel-crafts acylationof 6-alkoxy-2-pyrones: Preparation of substituted aromatics and anthraquinones. Tetrahedron Letters. 22: 3355-3358. DOI: 10.1016/S0040-4039(01)81903-1 |
0.474 |
|
| 1981 |
JUNG ME, HALWEG KM. ChemInform Abstract: INTRAMOLECULAR LEWIS ACID-PROMOTED (2+2) CYCLOADDITIONS: AN EFFICIENT TOTAL SYNTHESIS OF (.+-.)-CORONAFACIC ACID VIA AN INTERNAL DIELS-ALDER REACTION Chemischer Informationsdienst. 12. DOI: 10.1002/chin.198146193 |
0.346 |
|
| 1981 |
JUNG M, MILLER SJ. ChemInform Abstract: TOTAL SYNTHESIS OF ISOPAVINE AND INTERMEDIATES FOR THE PREPARATION OF SUBSTITUTED AMITRIPTYLINE ANALOGS: FACILE ROUTES TO SUBSTITUTED DIBENZOCYCLOOCTATRIENES AND DIBENZOCYCLOHEPTATRIENES Chemischer Informationsdienst. 12. DOI: 10.1002/chin.198130336 |
0.355 |
|
| 1980 |
Jung ME, Shapiro JJ. Synthesis and structure determination of 2-azabicyclo[2.2.1]hept-2-enes and their derivatives. W effect on chemical shifts Journal of the American Chemical Society. 102: 7862-7866. DOI: 10.1021/Ja00547A006 |
0.346 |
|
| 1980 |
Jung ME, Hudspeth JP. Total synthesis of (.+-.)-coronafacic acid: use of anionic oxy-Cope rearrangements on aromatic substrates in synthesis Journal of the American Chemical Society. 102: 2463-2464. DOI: 10.1021/Ja00527A059 |
0.433 |
|
| 1980 |
Jung ME, Pan Y. Direct stereoselective total synthesis of (±)-seychellene Tetrahedron Letters. 21: 3127-3130. DOI: 10.1016/S0040-4039(00)77426-0 |
0.451 |
|
| 1980 |
JUNG ME, PAN Y. ChemInform Abstract: DIRECT STEREOSELECTIVE TOTAL SYNTHESIS OF (.+-.)-SEYCHELLENE Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198047289 |
0.309 |
|
| 1980 |
JUNG ME, HUDSPETH JP. ChemInform Abstract: TOTAL SYNTHESIS OF (.+-.)-CORONAFACIC ACID: USE OF ANIONIC OXY-COPE REARRANGEMENTS ON AROMATIC SUBSTRATES IN SYNTHESIS Chemischer Informationsdienst. 11. DOI: 10.1002/CHIN.198028323 |
0.328 |
|
| 1980 |
JUNG ME, SHAW TJ, FRASER RR, BANVILLE J, TAYMAZ K. ChemInform Abstract: REINVESTIGATION OF THE REGIOSELECTIVITY OF DEPROTONATION OF KETONE DIMETHYLHYDRAZONES Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198005167 |
0.31 |
|
| 1979 |
Jung ME, Shaw TJ, R. Fraser R, Banville J, Taymaz K. Reinvestigation of the regioselectivity of deprotonation of ketone dimethylhydrazones Tetrahedron Letters. 20: 4149-4152. DOI: 10.1016/S0040-4039(01)86529-1 |
0.331 |
|
| 1979 |
Jung ME, Gaede B. Synthesis and diels-alder reactions of e-1-trimethylsilylbuta-1,3-diene Tetrahedron. 35: 621-625. DOI: 10.1016/0040-4020(79)87006-4 |
0.487 |
|
| 1979 |
JUNG ME, GAEDE B. ChemInform Abstract: SYNTHESIS AND DIELS-ALDER REACTIONS OF E-1-TRIMETHYLSILYLBUTA-1,3-DIENE Chemischer Informationsdienst. 10. DOI: 10.1002/chin.197925268 |
0.336 |
|
| 1979 |
JUNG ME, MOSSMAN AB, LYSTER MA. ChemInform Abstract: DIRECT SYNTHESIS OF DIBENZOCYCLOOCTADIENES VIA DOUBLE ORTHO FRIEDEL-CRAFTS ALKYLATION BY THE USE OF ALDEHYDE-TRIMETHYLSILYL IODIDE ADDUCTS Chemischer Informationsdienst. 10. DOI: 10.1002/CHIN.197903173 |
0.356 |
|
| 1978 |
JUNG ME, MAZUREK MA, LIM RM. A New Efficient Synthesis of Iodomethyl Methyl Ether Synthesis. 1978: 588-589. DOI: 10.1055/S-1978-24820 |
0.374 |
|
| 1978 |
Jung ME, Lyster MA. Conversion of alkyl carbamates into amines via treatment with trimethylsilyl iodide Journal of the Chemical Society, Chemical Communications. 315-316. DOI: 10.1039/C39780000315 |
0.446 |
|
| 1978 |
Jung ME, Lowe JA. Synthetic approaches to aclacinomycin and pyrromycin antitumour antibiotics via Diels–Alder reactions of 6-alkoxy-2-pyrones: total synthesis of chrysophanol, helminthosporin and pachybasin Journal of the Chemical Society, Chemical Communications. 95-96. DOI: 10.1039/C39780000095 |
0.389 |
|
| 1978 |
Jung ME, Mossman AB, Lyster MA. Direct synthesis of dibenzocyclooctadienes via double ortho Friedel-Crafts alkylation by the use of aldehyde-trimethylsilyl iodide adducts The Journal of Organic Chemistry. 43: 3698-3701. DOI: 10.1021/Jo00413A013 |
0.462 |
|
| 1978 |
Jung ME, McCombs CA. Total synthesis of (.+-.)-seychellene. Use of silyloxydienes in synthesis Journal of the American Chemical Society. 100: 5207-5209. DOI: 10.1021/Ja00484A051 |
0.395 |
|
| 1978 |
Jung ME, Hudspeth JP. Anionic oxy-Cope rearrangements with aromatic substrates in bicyclo[2.2.1]heptene systems. Facile synthesis of cis-hydrindanone derivatives, including steroid analogs Journal of the American Chemical Society. 100: 4309-4311. DOI: 10.1021/Ja00481A053 |
0.376 |
|
| 1978 |
JUNG ME, LYSTER MA. ChemInform Abstract: CONVERSION OF ALKYL CARBAMATES INTO AMINES VIA TREATMENT WITH TRIMETHYLSILYL IODIDE Chemischer Informationsdienst. 9. DOI: 10.1002/Chin.197830168 |
0.359 |
|
| 1978 |
JUNG ME, LOWE JA. ChemInform Abstract: SYNTHETIC APPROACHES TO ACLACINOMYCIN AND PYRROMYCIN ANTITUMOR ANTIBIOTICS VIA DIELS-ALDER REACTIONS OF 6-ALKOXY-2-PYRONES- TOTAL SYNTHESIS OF CHRYSOPHANOL, HELMINTHOSPORIN AND PACHYBASIN Chemischer Informationsdienst. 9. DOI: 10.1002/Chin.197824336 |
0.457 |
|
| 1977 |
Jung ME, Lowe JA. Synthetic approaches to adriamycin involving Diels-Alder reactions of photochemically generated bisketenes. Total synthesis of islandicin and digitopurpone Journal of Organic Chemistry. 42: 2371-2373. PMID 874615 DOI: 10.1021/Jo00434A005 |
0.458 |
|
| 1977 |
Jung ME, Pan Y, Rathke MW, Sullivan DF, Woodbury RP. Oxidation of trialkylsilyl enol ethers via hydride abstraction: a new procedure for ketone to enone conversion The Journal of Organic Chemistry. 42: 3961-3963. DOI: 10.1021/Jo00444A040 |
0.319 |
|
| 1977 |
Jung ME, Lyster MA. Quantitative dealkylation of alkyl ethers via treatment with trimethylsilyl iodide. A new method for ether hydrolysis The Journal of Organic Chemistry. 42: 3761-3764. DOI: 10.1021/Jo00443A033 |
0.335 |
|
| 1977 |
Jung ME, Hudspeth JP. Three-carbon annulation. Formation of five-membered rings from olefins via Diels-Alder reactions Journal of the American Chemical Society. 99: 5508-5510. DOI: 10.1021/Ja00458A060 |
0.39 |
|
| 1977 |
Jung ME, Andrus W, Ornstein PL. Non-aqueous conversion of ketals to ketones via treatment with trimethylsilyl iodide Tetrahedron Letters. 18: 4175-4178. DOI: 10.1016/S0040-4039(01)83458-4 |
0.303 |
|
| 1977 |
Jung ME, Shaw TJ. Stereospecificity in alkylation of anions of ketone dimethylhydrazones: kinetic preference, thermodynamic preference Tetrahedron Letters. 18: 3305-3308. DOI: 10.1016/S0040-4039(01)83225-1 |
0.342 |
|
| 1977 |
Jung ME, Ornstein PL. A new method for the efficient conversion of alcohols into iodides via treatment with trimethylsilyl iodide Tetrahedron Letters. 18: 2659-2662. DOI: 10.1016/S0040-4039(01)83039-2 |
0.372 |
|
| 1977 |
JUNG ME, LOWE JA. ChemInform Abstract: SYNTHETIC APPROACHES TO ADRIAMYCIN INVOLVING DIELS-ALDER REACTIONS OF PHOTOCHEMICALLY GENERATED BISKETENES. TOTAL SYNTHESIS OF ISLANDICIN AND DIGITOPURPONE Chemischer Informationsdienst. 8: no-no. DOI: 10.1002/Chin.197743168 |
0.467 |
|
| 1976 |
Jung ME, McCombs CA. 2-Trimethylsilyloxy-1,3-butadiene, a new reactive diene. Preparation and reactions Tetrahedron Letters. 17: 2935-2938. DOI: 10.1016/S0040-4039(01)85493-9 |
0.456 |
|
| 1976 |
Jung ME, Blair PA, Lowe JA. Reactions of oxime dianions: Stereospecificity in alkylation Tetrahedron Letters. 17: 1439-1442. DOI: 10.1016/S0040-4039(00)71277-9 |
0.44 |
|
| 1976 |
JUNG ME, MCCOMBS CA. ChemInform Abstract: 2-TRIMETHYLSILYLOXY-1,3-BUTADIENE, A NEW REACTIVE DIENE. PREPARATION AND REACTIONS Chemischer Informationsdienst. 7: no-no. DOI: 10.1002/chin.197644107 |
0.313 |
|
| 1976 |
JUNG ME, BLAIR PA, LOWE JA. ChemInform Abstract: REACTIONS OF OXIME DIANIONS- STEREOSPECIFICITY IN ALKYLATION Chemischer Informationsdienst. 7: no-no. DOI: 10.1002/chin.197631156 |
0.339 |
|
| 1975 |
JUNG ME. ChemInform Abstract: STEREOSELECTIVE SYNTHESIS OF SUBSTITUTED FUNCTIONALIZED BUTADIENES Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/Chin.197509196 |
0.427 |
|
| 1974 |
Jung ME. Stereoselective synthesis of substituted functionalized butadienes Journal of the Chemical Society, Chemical Communications. DOI: 10.1039/C3974000956B |
0.421 |
|
| 1974 |
Stork G, Jung ME, Colvin E, Noel Y. Synthetic routes to halomethyl vinylsilanes Journal of the American Chemical Society. 96: 3684-3686. DOI: 10.1021/Ja00818A071 |
0.527 |
|
| 1974 |
Stork G, Jung ME. Vinylsilanes as carbonyl precursors. Use in annelation reactions Journal of the American Chemical Society. 96: 3682-3684. DOI: 10.1021/Ja00818A070 |
0.589 |
|
| 1974 |
STORK G, JUNG ME. ChemInform Abstract: VINYLSILANES AS CARBONYL PRECURSORS. USE IN ANNELATION REACTIONS Chemischer Informationsdienst. 5: no-no. DOI: 10.1002/chin.197432349 |
0.303 |
|
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