Formate as a CO surrogate for cascade processes: Rh-catalyzed cooperative decarbonylation and asymmetric Pauson-Khand-type cyclization reactions.
暂无分享,去创建一个
[1] T. Shibata. Recent Advances in the Catalytic Pauson–Khand-Type Reaction , 2006 .
[2] A. Chan,et al. P-Phos: a family of versatile and effective atropisomeric dipyridylphosphine ligands in asymmetric catalysis. , 2006, Accounts of chemical research.
[3] A. Chan,et al. Iridium-catalyzed cascade decarbonylation/highly enantioselective Pauson–Khand-type cyclization reactions , 2006 .
[4] A. Chan,et al. A new class of versatile chiral-bridged atropisomeric diphosphine ligands: remarkably efficient ligand syntheses and their applications in highly enantioselective hydrogenation reactions. , 2006, Journal of the American Chemical Society.
[5] A. Chan,et al. Nickel-catalyzed asymmetric α-arylation of ketone enolates , 2006 .
[6] A. Chan,et al. Rhodium-BisbenzodioxanPhos complex-catalyzed homogeneous enantioselective pauson-khand-type cyclization in alcoholic solvents , 2005 .
[7] K. Takagi,et al. Iridium-catalyzed enantioselective Pauson-Khand-type reaction of 1,6-enynes , 2005 .
[8] A. Chan,et al. Rhodium-catalyzed asymmetric aqueous Pauson-Khand-type reaction. , 2005, Chemistry.
[9] S. Gibson,et al. The intermolecular Pauson-Khand reaction. , 2005, Angewandte Chemie.
[10] K. Park,et al. Immobilized Co/Rh Heterobimetallic Nanoparticle-Catalyzed Pauson–Khand-Type Reaction , 2005 .
[11] Y. Tu,et al. Rhodium-Catalyzed Asymmetric Pauson–Khand Reaction Using Monophosphoramidite Ligand SIPHOS , 2005 .
[12] J. Loch,et al. A study of [Co2(alkyne)(binap)(CO)4] complexes (BINAP=(1,1'-binaphthalene)-2,2'-diylbis(diphenylphosphine)). , 2005, Chemistry.
[13] G. Domínguez,et al. The Pauson-Khand reaction, a powerful synthetic tool for the synthesis of complex molecules. , 2004, Chemical Society reviews.
[14] K. Kakiuchi,et al. Catalytic asymmetric Pauson–Khand-type reactions of enynes with formaldehyde in aqueous media , 2004 .
[15] M. E. Krafft,et al. When the Pauson-Khand and Pauson-Khand type reactions go awry: a plethora of unexpected results , 2004 .
[16] K. Kakiuchi,et al. Evolution of carbonylation catalysis: no need for carbon monoxide. , 2004, Angewandte Chemie.
[17] G. Consiglio,et al. Mechanistic and stereochemical aspects of the asymmetric cyclocarbonylation of 1,6-enynes with rhodium catalysts. , 2004, Chemical Communications.
[18] A. Riera,et al. PuPHOS: a synthetically useful chiral bidentate ligand for the intermolecular Pauson-Khand reaction. , 2004, The Journal of organic chemistry.
[19] Nakcheol Jeong,et al. Desymmetrization of meso-dienyne by asymmetric Pauson-Khand type reaction catalysts. , 2004, Chemical communications.
[20] J. Genêt. Asymmetric catalytic hydrogenation. Design of new Ru catalysts and chiral ligands: from laboratory to industrial applications. , 2003, Accounts of chemical research.
[21] K. Park,et al. Immobilized heterobimetallic Ru/Co nanoparticle-catalyzed Pauson-Khand-type reactions in the presence of pyridylmethyl formate. , 2003, Chemical communications.
[22] S. Gibson,et al. The Pauson-Khand reaction: the catalytic age is here! , 2003, Angewandte Chemie.
[23] K. Takagi,et al. Catalytic Pauson-Khand-type reaction using aldehydes as a CO source. , 2002, Organic letters.
[24] S. Buchwald,et al. Cobalt-phosphite-catalyzed asymmetric Pauson-Khand reaction. , 2002, The Journal of organic chemistry.
[25] K. Kakiuchi,et al. CO-transfer carbonylation reactions. A catalytic Pauson-Khand-type reaction of enynes with aldehydes as a source of carbon monoxide. , 2002, Journal of the American Chemical Society.
[26] K. Takagi,et al. Iridium−Chiral Diphosphine Complex Catalyzed Highly Enantioselective Pauson-Khand-Type Reaction , 2000 .
[27] B. K. Sung,et al. Rhodium(I)-Catalyzed Asymmetric Intramolecular Pauson−Khand-Type Reaction , 2000 .
[28] R. Crabtree,et al. Aldehyde Decarbonylation Catalysis under Mild Conditions , 1999 .
[29] S. Buchwald,et al. Highly Enantioselective Catalytic Pauson−Khand Type Formation of Bicyclic Cyclopentenones , 1996 .
[30] G. Jenner. Homogeneous catalytic reactions involving methyl formate , 1995 .
[31] J. Clement,et al. Decarbonylation of formate esters by amines and phosphines , 1993 .
[32] S. Tantayanon,et al. Ruthenium complex catalyzed benzylation of arenes with benzyl formates; decarbonylation and decarboxylation of alkyl formates , 1989 .
[33] G. Jenner,et al. Ruthenium catalyzed decarbonylation of alkyl formates , 1989 .
[34] Y. Sasson,et al. Homogeneous decarbonylation of formate esters catalyzed by Vaska's compound , 1986 .
[35] D. Meek,et al. Catalytic Aspects of Metal Phosphine Complexes , 1982 .
[36] F. Calderazzo. Synthetic and Mechanistic Aspects of Inorganic Insertion Reactions. Insertion of Carbon Monoxide , 1977 .
[37] M. I. Foreman,et al. Organocobalt complexes. Part II. Reaction of acetylenehexacarbonyldicobalt complexes, (R1C2R2)Co2(CO)6, with norbornene and its derivatives , 1973 .