113. M. E. Jung, D. C. D'Amico, and W. Lew, "Efficient Total Synthesis of the Cytotoxic Halogenated Monoterpene Aplysiapyranoid A," Tetrahedron Lett. 1993, 34, 923.
114. M. E. Jung and C. Castro, "New Approach to the Synthesis of b-2'-Deoxyribonucleosides: Intramolecular Vorbrüggen Coupling," J. Org. Chem. 1993, 58, 807.
115. M. E. Jung and A. W. Sledeski, "Efficient Total Synthesis of Racemic and Optically Active Cyclobut-A and Simple Analogues," J. Chem. Soc., Chem. Commun. 1993, 589.
116. M. E. Jung, I. D. Trifunovich, and A. W. Sledeski, "A Simple Technique to Distinguish Between Cs and C2 Diastereomeric Diols Derived from Chiral Substrates," Heterocycles 1993, 35, 273.
117. M. E. Jung and A. Vidal Gomez, "Efficient Method for the Preparation of 2a,3b-Dichloro-4,4,10-trimethyldecalin Systems as a Route for the Synthesis of Dichlorolissoclimide," Tetrahedron Lett. 1993, 34, 2891.
118. M. E. Jung and C. S. Siedem, "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," J. Am. Chem. Soc. 1993, 115, 3822.
119. M. E. Jung and H. Rhee, "New Efficient Method for the Synthesis of the Antiviral Agent Carbovir," Tetrahedron Lett. 1993, 34, 4449.
120. M. E. Jung, C. N. Zimmerman, G. T. Lowen, and S. I. Khan, "Diastereocontrol in Intermolecular Diels-Alder Reactions of Allenic Lactones: Synthetic Approach to the Plaunols," Tetrahedron Lett. 1993, 34, 4453.
121. Y. Nagao, M. Takahashi, Y. Abe, T. Misono, and M. E. Jung, "Synthesis of 1,1-Dialkoxy Derivatives of 2,5-Diphenylsilacyclopent-3-ene and 2,5-Diphenylsilacyclopentane," Bull. Chem. Soc. Jpn. 1993, 66, 2294.
122. M. E. Jung and S. W. T. Choe, "Stereospecific Intramolecular Formyl Transfer via Radical Cyclization-Fragmentation: Preparation of Alkyl 2-Deoxy-2a-formylglycopyranosides and Similar Compounds," Tetrahedron Lett. 1993, 34, 6247.
123. M. E. Jung and D. C. D'Amico, "Enantiospecific Synthesis of All Four Diastereomers of 2-Methyl-3-((trialkylsilyl)oxy)alkanals: Facile Preparation of Aldols by Non-Aldol Chemistry," J. Am. Chem. Soc. 1993, 115, 12208.
124. M. E. Jung and H. L. Rayle, "An Improved Synthesis of 4-Methylene-2-cyclohexen-1-one," Synth. Commun. 1994, 24, 197.
125. M. E. Jung, C. H. Kim, and L. v. d. Bussche, "Vicarious Nucleophilic Aromatic Substitution via Trapping of an a-Ketosulfonium Ion Generated by a Pummerer-Type Rearrangement of 2-(Phenylsulfinyl)phenols: Preparation of Biaryls," J. Org. Chem. 1994, 59, 3248.
126. P. M. Harrington and M. E. Jung, "Stereoselective Bromination of a b-Ribofuranosyl Amide. Enantioselective Synthesis of (+)-Hydantocidin," Tetrahedron Lett. 1994, 35, 5145.
127. M. E. Jung and H. Rhee, "p-Allylpalladium Formation from Allylic Amines via N,N-Ditosylimides and N-Tosylamides: Efficient Synthesis of the Antiviral Agent Carbovir," J. Org. Chem. 1994, 59, 4719.
128. M. E. Jung and J. M. Gardiner, "Asymmetric Synthesis of Carbohydrates: Synthesis of 2-Deoxy-D- and 2-Deoxy-L-xylofuranosides from a Simple Achiral Precursor," Tetrahedron Lett. 1994, 35, 6755.
129. M. E. Jung and S. M. Dansereau, "Benzo[H]-1,6-naphthyridine Synthesis via Intramolecular Diels-Alder Reactions of Aryl Oxazoles: Synthetic Approach to 2-Bromoleptoclinidinone," Heterocycles 1994, 39, 767.
130. M. E. Jung, D. Jachiet, S. I. Khan, and C. Kim, "New Method for the Preparation of o-Aryloxyphenols: Pummerer-Type Rearrangement of an o-Hydroxyaryl Sulfoxide," Tetrahedron Lett. 1995, 36, 361.
131. M. E. Jung and S. W. T. Choe, "Total Synthesis of Cyclophellitol and (1R,2S)-Cyclophellitol from D-Mannose," J. Org. Chem. 1995, 60, 3280.
132. M. E. Jung and Y. H. Jung, "Efficient Enantioselective Synthesis of (2R,3S) Methyl b-Hydroxytyrosinate from Achiral Starting Materials," Synlett 1995, 563.
133. M. E. Jung and D. C. D'Amico, "Stereospecific Rearrangement of Optically Active Tertiary Allylic Epoxides to Give Optically Active Quaternary Aldehydes: Synthesis of a-Alkyl Amino Aldehydes and Acids," J. Am. Chem. Soc. 1995, 117, 7379.
134. M. E. Jung and M. Kiankarimi, "Gem-Dialkoxy Effect in Radical Cyclizations to Produce Cyclopropane Derivatives: Unusual Oxidation of a Dialkoxyalkyl Radical," J. Org. Chem. 1995, 60, 7013.
135. M. E. Jung and L. S. Starkey, "New Preparation of o-Aryloxyphenols via Cyclohexenone Oxides," Tetrahedron Lett. 1995, 36, 7363.
136. E. D. Murray, Jr., D. Kantoci, S. A. DeWind, A. E. Bigornia, D. C. D'Amico, J. G. King, Jr., T. Pham, B. H. Levine, M. E. Jung, and W. J. Wechter, "Endogenous Natriuretic Factors 3: Isolation and Characterization of Human Natriuretic Factors LLU-a, LLU-b1, and LLU-g," Life Sci. 1995, 57, 2145.
137. M. E. Jung, Y.-M. Cho, and Y. H. Jung, "Facile Synthesis of Optically Active 2-Hydroxymethyl-4-methylenecyclohexanol. Total De Novo Synthesis of Carbocyclic Sugars," Tetrahedron Lett. 1996, 37, 3.
138. M. E. Jung and T. Lazarova, "Preparation of (Phenylsulfinyl)phenols from Aryl Sulfinates: 'Thia-Fries Rearrangement'," Tetrahedron Lett. 1996, 37, 7.
139. M. E. Jung and B. T. Vu, "Substituent Effects on Intramolecular Dipolar Cycloadditions: The Gem-Dicarboalkoxy Effect," Tetrahedron Lett. 1996, 37, 451.
140. D. P. C. McGee, D. P. Sebesta, S. S. O'Rourke, R. L. Martinez, M. E. Jung, and W. A. Pieken, "Novel Nucleosides via Intramolecular Functionalization of 2,2'-Anhydrouridine Derivatives," Tetrahedron Lett. 1996, 37, 1995.
141. W. J. Wechter, D. Kantoci, E. D. Murray, Jr., D. C. D'Amico, M. E. Jung, and W.-H. Wang "A New Endogenous Natriuretic Factors: LLU-a," Proc. Natl. Acad. Sci. U. S. A. 1996, 93, 6002.
142. M. E. Jung and B. T. Vu, "Complete Diastereocontrol in Intramolecular 1,3-Dipolar Cycloadditions of 2-Substituted 5-Hexenyl and 5-Heptenyl Nitrones: Application to the Synthesis of the b-Lactam Antibiotic 1b-Methylthienamycin," J. Org. Chem. 1996, 61, 4427.
143. M. E. Jung and C. J. Nichols, "Highly Stereoselective Synthesis of trans, trans-4-Aryl-2,3-oxetanedimerthanols: Preparation of Oxetanocin A Analogues," Tetrahedron Lett. 1996, 37, 7667.
144. Y. Nagao, N. Namiki, S. Sakamoto, and M. E. Jung, "Synthesis of 2,5-Dimethyl and 2,5-Diphenylsilacyclopentane Derivatives and Their Reactions," in "43rd Symposium on Organometallic Chemistry," Kinki Chemical Society, Osaka, Japan, 1996, Abstract PA 112, pp. 50-1.
145. M. E. Jung and C. J. Nichols, "A Novel Tandem [1,2]-Brook/Retro-[1,6]-Brook Rearrangement of a 1-Trimethylsilyl-2,4-pentadien-1-ol Anion," J. Org. Chem. 1996, 61, 9065.
146. C. Giessner-Prettre, S. Hückel, J. Maddaluno, and M. E. Jung, ñMolecular Mechanics/ Continuum Reaction Field/Quantum Mechanics Study of the Intramolecular Diels-Alder Reaction of 2-Furfuryl Derivatives," J. Org. Chem. 1997, 62, 1439.
147. M. E. Jung and T. I. Lazarova, "Efficient Synthesis of Selectively Protected L-Dopa Derivatives from L-Tyrosine via Reimer-Tiemann and Dakin Reactions," J. Org. Chem. 1997, 62, 1531.
148. Y. Nagao, K. Miyakawa, S. Sakamoto, M. Takahashi, Y. Abe, and M. E. Jung, "Synthesis of trans-1,1-dialkoxy-2,5-diphenyl-1-sila-3-cyclopentenes and their 2-alkyl derivatives," Nippon Kagaku Kaishi 1997, 213.
149. M. E. Jung and K. L. Anderson, "Stereospecific Rearrangements of Optically Active 2-Aryl-3-Ethenyloxiranes to Give Optically Active b-Ethenylbenzeneethanols: Benzyl vs. Allyl Cations and an Efficient Synthesis of (S)-Ibuprofen," Tetrahedron Lett. 1997, 38, 2605.
150. M. E. Jung and Y. Xu, "Efficient Syntheses of L-Ribose and 2-Deoxy L-Ribose from D-Ribose and L-Arabinose," Tetrahedron Lett. 1997, 38, 4199.
151. M. E. Jung and L. S. Starkey, "Total Synthesis of S,S-Isodityrosine," Tetrahedron 1997, 53, 8815.
152. M. E. Jung and H. L. Rayle, "Generation of [5.5.n]Tricyclic Ring Systems by Radical Promoted Inter- and Intramolecular [3 + 2] Cycloadditions," J. Org. Chem. 1997, 62, 4601.
153. M. E. Jung and R. Marquez, "Gem-Disubstituent Effects in Small Ring Formation: Novel Ketal Ring Size Effect," Tetrahedron Lett. 1997, 38, 6521.
154. M. E. Jung and M. H. Parker, "Synthesis of Several Naturally Occurring Polyhalogenated Monoterpenes of the Halomon Class," J. Org. Chem. 1997, 62, 7094.
155. M. E. Jung and D. C. D'Amico, "Stereospecific Formation of Optically Active 2-([(Trialkylsilyl)-oxy]methyl)tetrahydrofuran-3-ols via Diastereoselective Epoxidation and Rearrangement of 5-[(Trialkylsilyl)oxy]-2-alken-1-ols," J. Am. Chem. Soc. 1997, 119, 12150.
156. M. E. Jung and T. W. Johnson, "Total Synthesis of 7-Deoxyxestobergsterol A, a Novel Pentacyclic Steroid of the Xestobergsterol Class," J. Am. Chem. Soc. 1997, 119, 12412.
157. M. E. Jung and S. Angelica, "An Intramolecular Prins Double Cyclization Catalyzed By Silyl Triflates," J. Org. Chem. 1997, 62, 9182.
158. M. E. Jung and C. J. Nichols, "Synthesis of Methylene-Expanded Oxetanocin Isonucleosides in Both Enantiomeric Forms," J. Org. Chem. 1998, 63, 347.
159. M. E. Jung and Y. Xu, "Efficient Synthesis of Specifically Deuterated Nucleosides: Preparation of 4'-Deuteriothymidine," Heterocycles 1998, 47, 349.
160. M. E. Jung and M. Kiankarimi, "Substituent and Solvent Effects in the Intramolecular Diels-Alder Reaction of 6-Furyl Hexenoates," J. Org. Chem. 1998, 63, 2968.
161. M. E. Jung and O. Kretschik, "Enantiospecific Total Synthesis of L-2',3'-Dideoxy Isonucleosides via Regioselective Opening of Optically Active C2-Symmetric 1,4-Pentadiene bis-Epoxide," J. Org. Chem. 1998, 63, 2975.
162. M. E. Jung and B. T. Fahr, "Total Synthesis of the Cytotoxic Marine Natural Product, Aplysiapyranoid C," J. Org. Chem. 1998, 63, 2982.
163. M. E. Jung and C. J. Nichols, "A de novo Synthesis of Ethyl 2-Deoxy-L-ribosides," Tetrahedron Lett. 1998, 39, 4615.
164. M. E. Jung, C. Castro, and S. I. Khan, "Novel Lewis Acid-Catalyzed Rearrangement of a Sugar-Base Hybrid to Afford an Anhydronucleoside," Nucleosides Nucleotides 1998,17, 2383.
165. M. E. Jung and M. Kiankarimi, "Synthesis of Methylene-Expanded 2',3'-Dideoxyribonucleosides," J. Org. Chem.1998,63, 8367.
166. M. E. Jung, U. Karama, and R. Marquez, "Conversion of Homoallylic Alcohols with Alkene Protection to the Corresponding Methyl Ketones," J. Org. Chem.1999,64, 663.
167. M. E. Jung, R. Marquez, and K. N. Houk, "Prediction of Variations in Efficiencies of 4-Exo Trig Radical Cyclizations," Tetrahedron Lett., 1999,40, 2661.
168. M. E. Jung and R. Marquez, "Rearrangement of Epoxides in Non-aldol Aldol Process: Allylic vs. Tertiary and Secondary Carbocationic Centers," Tetrahedron Lett., 1999,40, 3129.
169. M. E. Jung and N. Nishimura, "Stereoselective Formation of Formal Exo Diels-Alder Adducts of Silyloxydienes and Allenecarboxylates," J. Am. Chem. Soc. 1999, 121, 3529.
170. M. E. Jung and T. I. Lazarova, "New Efficient Method for the Total Synthesis of (S,S)-Isodityrosine from Natural Amino Acids," J. Org. Chem. 1999, 64, 2976.
171. M. E. Jung, "New Gem- and Vic-Disubstituent Effects on Cyclizations," Synlett 1999, 843.
172. M. E. Jung, C. J. Nichols, O. Kretschik, and Y. Xu, "Synthesis and Testing of New Modified Nucleosides," Nucleosides Nucleotides 1999,19, 541.
173. M. E. Jung, W. S. Lee, and D. Sun, "Extension of Non-aldol Aldol Process to Bis(propionates): Synthesis of Four Diastereomeric 3,5-Dialkoxy-2,4-dimethylalkanals,"Organic Lett., 1999,1, 307.
174. M. E. Jung and J. Pontillo, "Facile Preparation of Allenic Hydroxyketones via Rearrangement of Propargylic Alcohols," Organic Lett. 1999,1, 367.
175. A. D. Watson, G. Subbanagounder, D. S. Welsbie, K. F. Faull, M. Navab, M. E. Jung, A. M. Fogelman, and J. A. Berliner, "Structural Identification of a Novel Pro-inflammatory Epoxy Isoprostane Phospholipid in Mildly Oxidized Low Density Lipoprotein," J. Biol. Chem. 1999,274, 24787.
176. M. E. Jung and J. M. MacDougall, "First Enantioselective Total Synthesis of the Endogenous Natriuretic Agent LLU-a," Tetrahedron Lett. 1999,40, 6339.
177. M. E. Jung, W. Mengel, and T. L. Newton, "A Short, Convenient Synthesis of 2-Aryl-3,3-disubstituted Glycidic Esters via Organometallic Addition to a-Bromopyruvates," Synth. Commun. 1999,29, 3659.
178. M. E. Jung, E. C. Yang, B. T. Vu, M. Kiankarimi, E. Spyrou, and J. Kaunitz, "Glycosylation of Fluoroquinolones Through Direct and Oxygenated Polymethylene Linkages as a Sugar-Mediated Active Transport System for Antimicrobials," J. Med. Chem. 1999,42, 3899.
179. M. E. Jung and T. W. Johnson, "Unusual Cyclization Products Derived from Photolysis of Breslow's Steroidal Benzophenone Esters," J. Org. Chem. 1999,64, 7651.
180. M. E. Jung and U. Karama, "Highly Diastereoselective Markovnikov Hydration of 3,4-Dialkoxy-1-alkenes and 4,5-Dialkoxy-2-alkenes via a Hydroboration-Oxidation Process," Tetrahedron Lett. 1999,40, 7907.
181. M. E. Jung and Y. Xu, "Efficient Synthesis of 2-Deoxy L-Ribose from L-Arabinose: Mechanistic Information on the 1,2-Acyloxy Shift in Alkyl Radicals," Organic Lett. 1999,1,1517.
182. M. E. Jung and T. W. Johnson, "First Total Synthesis of Xestobergsterol A and Active Structural Analogues of the Xestobergsterols," Organic Lett. 1999,1, 1671.
183. M. E. Jung and D. Sun, "Stereoselective Production of b-Amino Alcohols and b-Thioacyl Alcohols via an Application of the non-Aldol Aldol Process," Tetrahedron Lett. 1999,40, 8343.
184. C. Castro, C. Chen, and M. E. Jung, "Intramolecular Glycosylation to form 2,6-Dioxo-4-methoxypyrimidine Nucleosides via O6,5'-Cyclonucleosides," Nucleosides Nucleotides 1999,18, 2415.
185. H. Rhee, D.-O. Yoon, and M. E. Jung, "Efficient Synthesis of the Carbocyclic Nucleoside, (±)-Homocarbovir via p­Allylpalladium Complex Formation from an Allyl N,N-Ditosylimide Substrate," Nucleosides Nucleotides 2000,19, 619.
186. A. S. Fraser, A. M. Kawasaki, M. E. Jung, and M. Manoharan, "An Efficient Method for the Synthesis of 2'-O-Modified Nucleosides Via Double Alkylation using Cyclic Sulfates," Tetrahedron Lett., 2000,41, 1423.
187. M. E. Jung and B. T. Fahr, "Novel Base-Induced [1,2]-Acyl Shift of Allylic Esters of Cyclopropane Carboxylic Acids," J. Org. Chem. 2000,65, 2239.
188. M. E. Jung and A. Toyota, "Efficient Synthesis of Several Methylene-Expanded Oxetanocin Nucleoside Analogues," Tetrahedron Lett., 2000,41, 3577.
189. M. E. Jung and R. Marquez, "Efficient Synthesis of the C1-C11 Fragment of the Tedanolides. The Non-aldol Aldol Process in Synthesis," Org. Lett., 2000, 2, 1669.
190. M. E. Jung, A. Huang, and T. W. Johnson, "Unusual Diastereoselectivity in Intramolecular Diels-Alder Reactions of Substituted 3,5-Hexadienyl Acrylates. Preference for a Boat-like Structure of the Six-Atom Tether due to Ester Overlap," Org. Lett., 2000, 2, 1835.
191. M. E. Jung and A. Huang, "Use of Optically Active Cyclic N,N-Dialkyl Aminals in Asymmetric Induction," Org. Lett., 2000, 2, 2659.
192. Y. Nagao, S. Sakamoto, K. Miyakawa, Y. Abe, and M. E. Jung, "Synthesis of 1-substituted derivatives of 2,5-diphenylsilacyclopent-3-enes and 2,5-diphenylsila-cyclopentanes," Nippon Kagaku Kaishi 2000, 411.
193.S. W. T. Choe and M. E. Jung, "Preparation of Various C-2 Branched Carbohydrates Using Stereospecific Intramolecular Radical Reactions," Carbohydr. Res. 2000, 329, 731.
194. M. E. Jung and C. P. Lee, "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 Lett. 2000, 41, 9719.
195. M. E. Jung and B. S. Lee, "Unusual a-Methylation of Alkoxyaryl Ketones with Higher Order Methyl Cuprate and Lithium Bromide," J. Org. Chem. 2000, 65, 9241.
196. M. E. Jung and C. P. Lee, "Synthesis of a Fully Functionalized Protected C1-C11 Fragment for the Synthesis of the Tedanolides," Org. Lett., 2001, 3, 333.
197. M. E. Jung and T. W. Johnson, "First Total Synthesis of Xestobergsterol A and Active Structural Analogues of the Xestobergsterols," Tetrahedron 2001, 57, 1449.
198. H. Cai, J. Strouse, D. Dumlao, M. E. Jung, and S. Clarke, "Distinct Reactions Catalyzed by Bacterial and Yeast trans-Aconitate Methyltransferases," Biochemistry 2001, 40, 2210.
199. M. E. Jung and P. Davidov, "First Conclusive Evidence of the Trapping of Primary Ozonides," Org. Lett. 2001, 3, 627.
200. D. J. Tantillo, K. N. Houk, and M. E. Jung, "Origins of Stereoselectivity in Intramolecular Diels-Alder Cycloadditions of Dienes and Dienophiles Linked by Ester and Amide Tethers," J. Org. Chem. 2001, 66, 1938.
201. M. E. Jung and A. Toyota, "Preparation of 4'-Substituted Nucleosides by Substitution of the Nucleoside 5'-Esters," J. Org. Chem. 2001, 66, 2624.
202. M. E. Jung and N. Nishimura, "Enantioselective Formal Total Synthesis of (-)-Dysidiolide," Org. Lett. 2001, 3, 2113.
203. M. E. Jung and F. Slowinski, "Rhodium-Catalyzed Decomposition of Indole-Substituted a-Diazo-b-Keto Esters: Three Different Reactions Based on Indole Oxidation State," Tetrahedron Lett. 2001, 42, 6835.
204. M. E. Jung and P. Davidov, "The First Reported Anionic Retro-Ene Reaction," Org. Lett. 2001, 3, 3025.
205. M. E. Jung, A. Toyota, E. De Clercq, and J. Balzarini, "Synthesis and Biological Activity of a Series of Methylene-Expanded Oxetanocin Nucleoside Analogues," Monatshefte Chem. 2002, 133, 499.
206. M. E. Jung and G. Piizzi, "Novel Rearrangements of 4-Silyl-3-buten-2-ones,"J. Org. Chem. 2002, 67, 3911.
207. M. E. Jung and J. Pontillo, "Synthetic Approach to Analogues of the Original Structure of Sclerophytin A," J. Org. Chem. 2002, 67, 6848.
208. M. E. Jung and P. D. Davidov, "Efficient Synthesis of a Tricyclic BCD Analogue of Ouabain: Lewis Acid Catalyzed Diels-Alder Reactions of Sterically Hindered Systems," Angew. Chemie, 2002, 41, 4125.
209. M. E. Jung and A. van den Heuvel, "Diastereoselectivity in non-Aldol Aldol Reactions: Silyl Triflate Promoted Payne Rearrangements," Tetrahedron Lett., 2002, 43, 8169.
210. M. E. Jung, A. Kers, G. Subbanagounder, and J. A. Berliner, "Endothelial Activation by an Epoxy Isoprostane Phsopholipid. Total Synthesis of Epoxy Isoprostanes," Chem Commun., 2003, 167.
211. M. E. Jung and G. Piizzi, "Synthesis of the A/B Ring System of Ouabain," Org. Lett., 2003, 5,137.
212. A. G. Leach, R. Wang, G. E. Wohlhieter, S. I. Khan, M. E. Jung, and K. N. Houk, "Theoretical Elucidation of Kinetic and Thermodynamic Control of Radical Addition Regioselectivity," J. Am. Chem. Soc. 2003, 125, 4271-78.
213. M. E. Jung and G. Piizzi, "Synthetic Approach to the AB Ring System of Ouabain," J. Org. Chem. 2003, 68, 2572-82.
214. M. E. Jung and J. Pontillo, "Synthetic Approach to Analogues of Sclerophytin A," Tetrahedron 2003, 59, 2729.
215. M. E. Jung, A. van den Heuvel, A. G. Leach, and K. N. Houk, "Unexpected Syn Hydride Migration in the Non-aldol Aldol Reaction," J. Am. Chem. Soc. , manuscript in preparation.
216. M. E. Jung, B. Hoffmann, and B. Rausch, "Use of Hindered Silyl Ethers as Protecting Groups for the Non-Aldol Aldol Process," manuscript in preparation.
217. M. E. Jung and A. van den Heuvel, "Tandem non-Aldol Aldol-Mukaiyama Aldol Process: Synthesis of Bis-b-Silyloxy)ketones," Tetrahedron Lett., submitted for publication.
218. M. E. Jung and J. Wasserman, "A Simple Efficient Synthesis of Vinyl Chlorides and gem-Dichlorides from Ketones," manuscript in preparation.

NOTE: Check out the interesting (and unusual) publication by M. E. Jung: Crostic No. 49 in Crostics, No. 115, Simon & Schuster, New York, NY, ed. T. H. Middleton, 1996.