Münchnones--new facets after 50 years.

[1]  B. Arndtsen,et al.  Chiral phosphorus-based 1,3-dipoles: a modular approach to enantioselective 1,3-dipolar cycloaddition and polycyclic 2-pyrroline synthesis. , 2014, Organic letters.

[2]  N. Martín,et al.  Enantioselective Cycloaddition of Münchnones onto [60]Fullerene: Organocatalysis versus Metal Catalysis , 2014, Journal of the American Chemical Society.

[3]  R. Larock,et al.  Aryne Cycloaddition with Stable Münchnones: Synthesis of 9,10‐Dihydro‐9,10‐epiminoanthracenes and Isoindoles , 2014 .

[4]  K. Houk,et al.  Modular mesoionics: understanding and controlling regioselectivity in 1,3-dipolar cycloadditions of Münchnone derivatives. , 2013, Journal of the American Chemical Society.

[5]  B. Arndtsen,et al.  Transition-metal-catalyzed multicomponent coupling reactions with imines and carbon monoxide , 2013 .

[6]  F. Toste,et al.  Gold(I)-catalyzed diastereo- and enantioselective 1,3-dipolar cycloaddition and Mannich reactions of azlactones. , 2011, Journal of the American Chemical Society.

[7]  B. Arndtsen,et al.  A palladium-catalyzed multicomponent synthesis of imidazolinium salts and imidazolines from imines, acid chlorides, and carbon monoxide. , 2011, The Journal of organic chemistry.

[8]  B. Arndtsen,et al.  Palladium catalyzed synthesis of münchnones from alpha-amidoethers: a mild route to pyrroles. , 2008, Angewandte Chemie.

[9]  B. Arndtsen,et al.  A new use of Wittig-type reagents as 1,3-dipolar cycloaddition precursors and in pyrrole synthesis. , 2007, Journal of the American Chemical Society.

[10]  B. Arndtsen,et al.  Direct synthesis of pyrroles from imines, alkynes, and acid chlorides: an isocyanide-mediated reaction. , 2007, Organic letters.

[11]  J. Tepe,et al.  Stereoselective synthesis of highly substituted Delta1-pyrrolines: exo-selective 1,3-dipolar cycloaddition reactions with azlactones. , 2004, Journal of the American Chemical Society.

[12]  G. Gribble Mesoionic Ring Systems , 2003 .

[13]  C. A. Ramsden,et al.  Heterocyclic mesomeric betaines , 1985 .

[14]  H. Bayer,et al.  1.3‐Dipolare Cycloadditionen, LVI. Eine bequeme Synthese von N‐substituierten Pyrrolen aus mesoionischen Oxazolonen und Alkinen , 1970 .

[15]  H. Bayer,et al.  Azlactone als 1.3-Dipole. Eine neue Synthese von Pyrrolen , 1964 .

[16]  R. Huisgen,et al.  A New Type of Mesoionic Aromatic Compound and Its 1,3‐Dipolar Cycloaddition Reactions with Acetylene Derivatives , 1964 .

[17]  R. Schmidt,et al.  1,3‐Dipolar Additions of Sydnones to Alkynes. A New Route into the Pyrazole Series , 1962 .

[18]  R. Schmidt,et al.  1.3-Dipolare Additionen der Sydnone an Alkine. Ein neuer Weg in die Pyrazol-Reihe , 1962, Angewandte Chemie.

[19]  J. Campbell Earl,et al.  204. The action of acetic anhydride on N-nitrosophenylglycine and some of its derivatives , 1935 .

[20]  G. Lunge Zur gasvolumetrischen Analyse durch Wasserstoffsuperoxyd , 1890 .