Nucleophilic Ring‐Opening of N‐o‐Nosylaziridines with N‐Chloro‐N‐Sodiocarbamate: Facile Preparation of Differentially Protected Vicinal Diamines

[1]  S. Stankovic,et al.  Regioselectivity in the ring opening of non-activated aziridines. , 2012, Chemical Society reviews.

[2]  S. Minakata,et al.  Diastereoselective aziridination of chiral electron-deficient olefins with N-chloro-N-sodiocarbamates catalyzed by chiral quaternary ammonium salts. , 2011, The Journal of organic chemistry.

[3]  D. Du,et al.  Development of Diphenylamine‐Linked Bis(imidazoline) Ligands and Their Application in Asymmetric Friedel–Crafts Alkylation of Indole Derivatives with Nitroalkenes , 2010 .

[4]  P. Lu Recent Developments in Regioselective Ring Opening of Aziridines , 2010 .

[5]  F. Cardona,et al.  Metal-catalysed 1,2-diamination reactions. , 2009, Nature chemistry.

[6]  V. Gotor,et al.  trans-cyclopentane-1,2-diamine: the second youth of the forgotten diamine. , 2009, Chemical Society reviews.

[7]  S. Minakata Utilization of N-X bonds in the synthesis of N-heterocycles. , 2009, Accounts of chemical research.

[8]  C. Schneider Katalytische enantioselektive Ringöffnungen von Aziridinen , 2009 .

[9]  C. Schneider Catalytic, enantioselective ring opening of aziridines. , 2009, Angewandte Chemie.

[10]  Renata Marcia de Figueiredo Übergangsmetall‐katalysierte Diaminierung von Alkenen , 2009 .

[11]  R. M. Figueiredo Transition‐Metal‐Catalyzed Diamination of Olefins , 2009 .

[12]  B. Kim,et al.  Preparation of Chiral Diamines by the Diaza-Cope Rearrangement (DCR) , 2009 .

[13]  C. Hövelmann,et al.  First palladium- and nickel-catalyzed oxidative diamination of alkenes: Cyclic urea, sulfamide, and guanidine building blocks , 2008 .

[14]  S. Minakata,et al.  Practical and convenient synthesis of N-heterocycles: stereoselective cyclization of N-alkenylamides with t-BuOI under neutral conditions. , 2006, Organic letters.

[15]  C. Timmons,et al.  Vicinal Diamino Functionalities as Privileged Structural Elements in Biologically Active Compounds and Exploitation of their Synthetic Chemistry , 2006, Chemical biology & drug design.

[16]  E. Jacobsen,et al.  General catalytic synthesis of highly enantiomerically enriched terminal aziridines from racemic epoxides. , 2004, Angewandte Chemie.

[17]  X. Eric Hu,et al.  Nucleophilic ring opening of aziridines , 2004 .

[18]  E. Muñoz,et al.  Manipulating L‐Aspartic and L‐Glutamic Acids − Diastereoselective Synthesis of Enantiopure β‐Amino‐γ‐hydroxy Acids and γ‐Amino‐δ‐hydroxy Acids , 2003 .

[19]  G. Bridger,et al.  Facile synthesis of a selectively protected triazamacrocycle , 2002 .

[20]  J. Sweeney Aziridines: epoxides' ugly cousins? , 2002, Chemical Society reviews.

[21]  T. Hudlický,et al.  Opening of a vinyl aziridine with p-toluenesulfonamide under TBAF catalysis: synthesis of 3,4-diamino-3,4-dideoxy-l-chiro-inositol , 2001 .

[22]  T. Yamane,et al.  2-nitro- and 2,4-dinitrobenzenesulfonamides as protecting groups for primary amines , 2001 .

[23]  I. Ryu,et al.  Iodine-catalyzed aziridination of alkenes using Chloramine-T as a nitrogen source , 1998 .

[24]  C. Mioskowski,et al.  The Chemistry of Vicinal Diamines. , 1998, Angewandte Chemie.

[25]  C. Mioskowski,et al.  Die Chemie vicinaler Diamine , 1998 .

[26]  W G Laver,et al.  Structure-activity relationship studies of novel carbocyclic influenza neuraminidase inhibitors. , 1998, Journal of medicinal chemistry.

[27]  S. Hanessian,et al.  trans-1,2-Diaminocyclohexane Derivatives as Chiral Reagents, Scaffolds, and Ligands for Catalysis: Applications in Asymmetric Synthesis and Molecular Recognition. , 1997, Chemical reviews.

[28]  M. Cheung,et al.  3- AND 4-NITROBENZENESULFONAMIDES : EXCEPTIONALLY VERSATILE MEANS FOR PREPARATION OF SECONDARY AMINES AND PROTECTION OF AMINES , 1995 .

[29]  D. Nowotnik,et al.  Synthesis of nitroimidazole substituted 3,3,9,9-tetramethyl-4,8-diazaundecane-2,10-dione dioximes (propylene amine oximes, PnAOs): Ligands for technetium-99m complexes with potential for imaging hypoxic tissue , 1995 .

[30]  D. Tanner Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations , 1994 .

[31]  David P. Tanner Chirale Aziridine — Herstellung und stereoselektive Transformationen , 1994 .

[32]  C. Tomasini,et al.  Synthesis of (R)-N-Tosylemeriamine via Chiral N-Tosylimidazolidin-2-ones , 1990 .

[33]  S Shinagawa,et al.  Chemistry and inhibitory activity of long chain fatty acid oxidation of emeriamine and its analogues. , 1987, Journal of medicinal chemistry.

[34]  P. Nunn,et al.  Guam amyotrophic lateral sclerosis-parkinsonism-dementia linked to a plant excitant neurotoxin. , 1987, Science.

[35]  H. Iwatsuka,et al.  Emeriamine, an antidiabetic β-aminobetaine derived from a novel fungal metabolite , 1985 .

[36]  P. von Voigtlander,et al.  Benzeneacetamide amines: structurally novel non-m mu opioids. , 1982, Journal of medicinal chemistry.

[37]  K. B. Sharpless,et al.  Osmium-catalyzed vicinal oxyamination of olefins by N-chloro-N-metallocarbamates , 1980 .

[38]  I. Page,et al.  Synthesis of a Biologically Active Octapeptide Similar to Natural Isoleucine Angiotonin Octapeptide1 , 1957 .