A concise synthesis of (-)-oseltamivir.

[1]  M. Kanai,et al.  Synthetic Strategies for Oseltamivir Phosphate , 2008 .

[2]  Kyle D. Baucom,et al.  Rh(II)-catalyzed intermolecular oxidative sulfamidation of aldehydes: a mild efficient synthesis of N-sulfonylcarboxamides. , 2007, Journal of the American Chemical Society.

[3]  An-Suei Yang,et al.  Synthesis of tamiflu and its phosphonate congeners possessing potent anti-influenza activity. , 2007, Journal of the American Chemical Society.

[4]  D. Hagberg,et al.  An iron carbonyl approach to the influenza neuraminidase inhibitor oseltamivir. , 2007, Chemical communications.

[5]  T. Fukuyama,et al.  A practical synthesis of (-)-oseltamivir. , 2007, Angewandte Chemie.

[6]  M. Kanai,et al.  A concise synthesis of Tamiflu: third generation route via the Diels–Alder reaction and the Curtius rearrangement , 2007 .

[7]  M. Kanai,et al.  Second generation catalytic asymmetric synthesis of Tamiflu: allylic substitution route. , 2007, Organic letters.

[8]  K. W. Fiori,et al.  Catalytic intermolecular amination of C-H bonds: method development and mechanistic insights. , 2007, Journal of the American Chemical Society.

[9]  Paul M Wehn,et al.  Rh-catalyzed alkene oxidation: a highly efficient and selective process for preparing N-alkoxysulfonyl aziridines , 2006 .

[10]  V. Farina,et al.  Tamiflu: the supply problem. , 2006, Angewandte Chemie.

[11]  Vittorio Farina,et al.  Tamiflu: Das Versorgungsproblem , 2006 .

[12]  Zigang Li,et al.  Nitrene transfer reactions catalyzed by gold complexes. , 2006, The Journal of organic chemistry.

[13]  Z. Yao,et al.  Ring-closing metathesis-based synthesis of (3R,4R,5S)-4-acetylamino-5-amino-3-hydroxy- cyclohex-1-ene-carboxylic acid ethyl ester: a functionalized cycloalkene skeleton of GS4104. , 2006, The Journal of organic chemistry.

[14]  M. Kanai,et al.  De novo synthesis of Tamiflu via a catalytic asymmetric ring-opening of meso-aziridines with TMSN3. , 2006, Journal of the American Chemical Society.

[15]  E. Corey,et al.  A short enantioselective pathway for the synthesis of the anti-influenza neuramidase inhibitor oseltamivir from 1,3-butadiene and acrylic acid. , 2006, Journal of the American Chemical Society.

[16]  J. Halfen.  Recent Advances in Metal-Mediated Carbon-Nitrogen Bond Formation Reactions: Aziridination and Amidation , 2005 .

[17]  Christine G. Espino,et al.  Expanding the scope of C-H amination through catalyst design. , 2004, Journal of the American Chemical Society.

[18]  P. Harrington,et al.  The synthetic development of the anti-influenza neuraminidase inhibitor oseltamivir phosphate (Tamiflu®): A challenge for synthesis & process research , 2004 .

[19]  Yong Cui,et al.  Efficient aziridination of olefins catalyzed by a unique disilver(I) compound. , 2003, Journal of the American Chemical Society.

[20]  J. Du Bois,et al.  A unique and highly efficient method for catalytic olefin aziridination. , 2002, Journal of the American Chemical Society.

[21]  B. Trost,et al.  Asymmetric Alkylation of Nitroalkanes , 2000 .

[22]  K. Kent,et al.  Practical Total Synthesis of the Anti-Influenza Drug GS-4104 , 1998 .

[23]  W G Laver,et al.  Influenza neuraminidase inhibitors possessing a novel hydrophobic interaction in the enzyme active site: design, synthesis, and structural analysis of carbocyclic sialic acid analogues with potent anti-influenza activity. , 1997, Journal of the American Chemical Society.

[24]  Barry M. Trost and,et al.  On the Question of the Symmetry of Formally Symmetrical π-(Allyl)palladium Cationic Intermediates in Allylic Alkylations , 1996 .

[25]  B. Trost,et al.  New synthetic reactions. A chemoselective approach to cleavage .alpha. to a carbonyl group via .beta.-keto sulfides. Preparation of 1,2-diketones , 1977 .