Accoun ts Letters - Thieme Chemistry

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Letters VIII Table of Contents 1274 A Facile Synthesis of 3’-Deoxy-3’-fluorothymidine via a Highly Stereoselective Glycosylation with 2,3- Dideoxy-3-fluoro-D-erythro-pentofuranosyl Diethyl Phosphite J. Inagaki, H. Sakamoto, M. Nakajima, S. Nakamura, S. Hashimoto 1277 Polymer-Supported Acid Catalyst in the Carbon- Carbon Bond Formation of Acetals with Silylated Nucleophiles N. Tanaka, Y. Masaki 1280 Treatment of N-Boc Derivatives of b-Amino Alcohols with N,N-Diethylaminosulfur Trifluoride Leads to Chiral Oxazolidinones: An Unexpected Intramolecular Cyclization H. Zhao, A. Thurkauf 1283 A New and Extremely Active Corey’s Chiral Oxazaborolidine Catalyst K. Ishihara, S. Kondo, H. Yamamoto 1286 Sulfur-Controlled Exo Selective Aryl Radical Cyclization onto Exo-Methylenecycloalkanes H. Ishibashi, T. Kobayashi, D. Takamasu 1289 A Novel Carbocyclic Ring Closure of Hex-5enopyranosides and Pent-4-enofuranosides J. K. Gallos, T. V. Koftis, A. E. Koumbis, V. I. Moutsos OTMS O N Me HN Me BzO O TMSO N (1.5 equiv.) BzO F OP(OEt)2 TMSOTf (1.0 equiv.) EtCN, -50 °C, 30 min α:β=64:36 R OMe OMe (50 mg) NC NC O O N O Ot DAST CH2F Bu O O O O polymer cat. (50 mg), TMS-Nu (1.5 eq.) CH 3CN, reflux R = aryl, aliphatic, α,β-unsaturated Nu = CN, CH2COPh, CH2CO-2-Furyl N O Ot CH2OH DAST Bu SPh PhS Br Bu3SnH AIBN ( )n ( ) n O O N F β:α=91:9 R OMe Nu N O O
Table of Contents IX 1292 Highly Enantioselective Synthesis of Substituted Piperidines using the Chiral Lithium Amide Base Approach N. J. Goldspink, N. S. Simpkins, M. Beckmann 1295 Chemistry of Insect Antifeedants from Azadirachta indica (Part 22): Functionalisation of the Decalin Fragment of Azadirachtin via a Claisen Rearrangement Reaction S. V. Ley, C. E. Gutteridge, A. R. Pape, C. D. Spilling, C. Zumbrunn 1298 The Baker’s Yeast Reduction of the b-Keto Aldehydes in the Presence of a Sulfur Compound R. Hayakawa, M. Shimizu 1301 N-Carboalkoxy-2-Nitrobenzenesulfonamides: A Practical Preparation of N-Boc-, N-Alloc-, and N-Cbz-Protected Primary Amines T. Fukuyama, M. Cheung, T. Kan 1304 Triazenes: A Useful Protecting Strategy for Sensitive Secondary Amines R. Lazny, J. Poplawski, J. Köbberling, D. Enders, S. Bräse 1307 Diastereoselectivity in Michael Additions to a Pyrrolidinyl Enone R. W. Bates, P. Kongsaeree MeO2C TESO MeO2C R 1 N CO2Me Bn H O Ph MeO2C TESO O OBnR2 O Ph N Li Ph N Li Ph THF, -78 °C electrophile (≥ 98% ee) R 1 O OH H R2 R1 O OH R2 R1 OH R2 Baker's Yeast Sulfur-Compound N O Ot DAST CH2F Bu ∆ MeO 2C TESO MeO2C H O N CO2Me Bn E MeO2C TESO O OBn R2 R OH 1 N O Ot CH2OH DAST Bu OH R 2 O OH N O O R 1 Letters
Page 1 and 2: 1181 Insoluble Polymer-Bound (IPB)
Page 3 and 4: Table of Contents V 1235 Formation
Page 5: Table of Contents VII 1259 Unexpect
Page 9 and 10: Table of Contents XI 1328 Organic S

Accoun ts Letters - Thieme Chemistry

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