Optimisation and scale-up of microwave assisted cyanation
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[1] N. Leadbeater. Fast, easy, clean chemistry by using water as a solvent and microwave heating: the Suzuki coupling as an illustration. , 2005, Chemical communications.
[2] R. Chidambaram. A robust palladium-catalyzed cyanation procedure: beneficial effect of zinc acetate , 2004 .
[3] C. Crouzel,et al. [11C]copper(I) cyanide: a new radioactive precursor for 11C-cyanation and functionalization of haloarenes , 1997 .
[4] J. Tierney,et al. Microwave assisted organic synthesis-a review , 2001 .
[5] J. Tierney,et al. Microwave Assisted Organic Synthesis , 2005 .
[6] J. Wepsiec,et al. Cooperative Catalyst Effects in Palladium-Mediated Cyanation Reactions of Aryl Halides and Triflates , 1998 .
[7] D. Tschaen,et al. An Improved Procedure for Aromatic Cyanation , 1994 .
[8] K. Jähnisch,et al. Oxidation and Ammoxidation of Aromatics , 2004 .
[9] K. Takagi,et al. The Cyanation of Aromatic Halides Catalyzed by Nickel(0) Complexes Generated In Situ. I. General Scope and Limitations , 1988 .
[10] M. Beller,et al. An environmentally benign procedure for the Cu-catalyzed cyanation of aryl bromides , 2005 .
[11] A. Loupy. Microwaves in organic synthesis , 2002 .
[12] S. Caddick,et al. Microwave assisted organic reactions , 1995 .
[13] K. Sasaki,et al. The Cyanation of Aromatic Halides Catalyzed by Nickel(0) Complexes Generated in Situ. II. The Cyanation of Heteroaromatic Halides , 1993 .
[14] G. P. Ellis,et al. Cyanation of aromatic halides , 1987 .
[15] M. J. Collins,et al. Automated batch scale-up of microwave-promoted Suzuki and Heck coupling reactions in water using ultra-low metal catalyst concentrations , 2005 .
[16] A. Gogoll,et al. Rapid homogeneous-phase Sonogashira coupling reactions using controlled microwave heating. , 2001, The Journal of organic chemistry.
[17] M. Beller,et al. A new palladium catalyst system for the cyanation of aryl chlorides , 2001 .
[18] M. Beller,et al. Palladium‐Catalyzed Cyanation of Aryl Halides: Recent Developments and Perspectives , 2003 .
[19] M. Beller,et al. Progress in the palladium-catalyzed cyanation of aryl chlorides. , 2003, Chemistry.
[20] M. Beller,et al. Potassium hexacyanoferrate(II)--a new cyanating agent for the palladium-catalyzed cyanation of aryl halides. , 2004, Chemical communications.
[21] P. Walla,et al. Microwave-assisted Negishi and Kumada cross-coupling reactions of aryl chlorides. , 2004, Chemical communications.
[22] P. Walla,et al. Scalability of Microwave-Assisted Organic Synthesis. From Single-Mode to Multimode Parallel Batch Reactors , 2003 .
[23] P. Confalone,et al. Palladium-catalyzed cyanation reactions of aryl chlorides , 2000 .
[24] J. M. Williams,et al. Palladium-catalyzed cyanation of aryl bromides promoted by low-level organotin compounds. , 2004, Organic letters.
[25] M. Beller,et al. A convenient procedure for the palladium-catalyzed cyanation of aryl halides. , 2003, Angewandte Chemie.
[26] Y. Liu,et al. An investigation into causes and effects of high cyanide levels in the palladium-catalyzed cyanation reaction. , 2004, Organic letters.
[27] F. Fleitz,et al. A highly catalytic robust palladium catalyzed cyanation of aryl bromides , 1999 .
[28] J. Neumeyer,et al. Microwave-promoted Pd-catalyzed cyanation of aryl triflates: a fast and versatile access to 3-cyano-3-desoxy-10-ketomorphinans. , 2003, Organic letters.
[29] M. Beller,et al. A convenient and efficient procedure for the palladium-catalyzed cyanation of aryl halides using trimethylsilylcyanide , 2003 .
[30] G. Palmisano,et al. Statistical experimental design-driven discovery of room-temperature conditions for palladium-catalyzed cyanation of aryl bromides , 2005 .
[31] Nicholas E. Leadbeater,et al. An assessment of the technique of simultaneous cooling in conjunction with microwave heating for organic synthesis , 2005 .
[32] C. Kappe,et al. Controlled microwave heating in modern organic synthesis. , 2004, Angewandte Chemie.
[33] Alterman,et al. Fast microwave-assisted preparation of aryl and vinyl nitriles and the corresponding tetrazoles from organo-halides , 2000, The Journal of organic chemistry.
[34] N. Leadbeater,et al. Rapid, easy cyanation of aryl bromides and chlorides using nickel salts in conjunction with microwave promotion. , 2003, The Journal of organic chemistry.
[35] M. Hatsuda,et al. A practical synthesis of highly functionalized aryl nitriles through cyanation of aryl bromides employing heterogeneous Pd/C , 2005 .