Metal-free activation of CO2 by mesoporous graphitic carbon nitride.

[1]  M. Antonietti,et al.  Metal-free catalysis of sustainable Friedel-Crafts reactions: direct activation of benzene by carbon nitrides to avoid the use of metal chlorides and halogenated compounds. , 2006, Chemical communications.

[2]  M. Antonietti,et al.  Chemical synthesis of mesoporous carbon nitrides using hard templates and their use as a metal-free catalyst for Friedel-Crafts reaction of benzene. , 2006, Angewandte Chemie.

[3]  Arne Thomas,et al.  Chemische Synthese von mesoporösen Kohlenstoffnitriden in harten Templaten und ihre Anwendung als metallfreie Katalysatoren in Friedel‐Crafts‐Reaktionen , 2006 .

[4]  R. Srivastava,et al.  Sites for CO2 activation over amine-functionalized mesoporous Ti(Al)-SBA-15 catalysts , 2006 .

[5]  W. Schnick,et al.  From Triazines to Heptazines , 2006 .

[6]  A. J. Kropf,et al.  Studies of Cu-ZSM-5 by X-ray absorption spectroscopy and its application for the oxidation of benzene to phenol by air , 2005 .

[7]  N. Bofinger,et al.  POSSIBLE ORIGIN FOR PORPHIN DERIVATIVES IN PREBIOTIC CHEMISTRY – A COMPUTATIONAL STUDY , 2005, Origins of Life and Evolution of Biospheres.

[8]  C. Eckert,et al.  The reaction of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) with carbon dioxide. , 2005, The Journal of organic chemistry.

[9]  G. Domínguez,et al.  The Pauson-Khand reaction, a powerful synthetic tool for the synthesis of complex molecules. , 2004, Chemical Society reviews.

[10]  I. Nakamura,et al.  Transition-metal-catalyzed reactions in heterocyclic synthesis. , 2004, Chemical reviews.

[11]  D. W. Franco,et al.  Efficient and clean synthesis of N-alkyl carbamates by transcarboxylation and O-alkylation coupled reactions using a DBU–CO2 zwitterionic carbamic complex in aprotic polar media , 2002 .

[12]  J. R. Moss,et al.  Recent developments in the activation of carbon dioxide by metal complexes , 1999 .

[13]  Sven Rau,et al.  Carbon dioxide and metal centres: from reactions inspired by nature to reactions in compressed carbon dioxide as solvent , 1999 .

[14]  F. C. Hartman,et al.  Mechanism of Rubisco: The Carbamate as General Base. , 1998, Chemical reviews.

[15]  D. Riley,et al.  Palladium-catalyzed generation of O-allylic urethanes and carbonates from amines/alcohols, carbon dioxide, and allylic chlorides , 1993 .

[16]  G. Wachtershauser.  The cradle chemistry of life: On the origin of natural products in a pyrite-pulled chemoautotrophic origin of life , 1993 .

[17]  E. Imoto,et al.  CARBOXYLATION OF ACTIVE METHYLENE COMPOUNDS USING THE REAGENT OF 1,8-DIAZABICYCLO(5.4.0)-7-UNDECENE AND CARBON DIOXIDE , 1974 .

[18]  G. Chiusoli,et al.  Superbase catalysis of oxazolidin-2-one ring formation from carbon dioxide and prop-2-yn-1-amines under homogeneous or heterogenous conditions , 1998 .

[19]  G. Wächtershäuser,et al.  Evolution of the first metabolic cycles. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[20]  R. Back,et al.  High-temperature photolysis and the pyrolysis of formamide vapour, and the thermal decomposition of the carbamyl radical , 1971 .