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Your review was sent successfully and is now waiting for our team to publish it. Unless there is a switch to Many important synthetic organic reaction protocols involve different wavelengths, to allow increased penetration of insoluble reagents or catalysts that can not be substituted in reaction mixtures, reactors similar to the presented 1 m3 all cases for soluble alternatives. With respect to building prototype of Sairem will be at the very end of the scale-up larger flow reactors, many scientists in the field are range. The question if specific or non-thermal microwave effects do exist, therefore, needs to be addressed in a serious manner by the scientific community.

Figure Custom-made 1 m3 batch recycle reactor for the pro- reactor part. Gabriel, S. Gabriel, E. Grant, B. Halstead, ve-assisted flow processing is not easy, and at this stage no D. Mingos, Chem. Mingos, D. Baghurst, Chem. Kremsner, A. Stadler, C. Kappe, Topics Curr. Strauss, R. Trainor, Aust. Strauss, Aust. Roberts, C. Loupy, Ed. Keywords: batch reactors; continuous flow; microwave heating; [14] For a recent review on continuous flow organic chemistry, processing; synthesis see: G.

Associated Data

Jas, A. Kirschning, Chem. Kirschning, W. Solodenko, K. Mennecke, Chem. Strauss, A. Feher, [1] H. Kingston, S.

Organic synthesis practical techniques

Fagrell; [16d] American Chemical Society, Washington Gedye, F. Smith, K. Westway, H.

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Ali, L. Baldisera, M. Collins, M. Collins, Jr. Hargett, Jr. King, L. Laberge, J. Rusell, Tetrahedron Lett. Giguere, T. Bray, S. Duncan, G. Majetich, Tetrahedron invs. King, J. Lambert, Lett. Smith, J. Westway, Can. Schwalbe, K. Today , 24, 56; [17b] I. Baxendale, M. Today , 24, Matthews, NC ; [3c] P. Hessel, H. Baerns, Angew.

Fletcher, S. Haswell, Oxford ; [3d] C. Kappe, A. Pombo-Villar, B. Warrington, P. Watts, S. Zhang, Tetrahedron , 58, ; [18c] H. Pennemann, ; [3e] A. Haswell, V.

Named Reactions

Process Res. Larhed, , 8, ; [18d] S. Taghavi-Moghadam, A. Kleemann, K. Golbig, Org. Ehrfeld, V. Kappe, Angew. Hayes, Aldrichim.

Microwave-assisted Organic Synthesis

Acta , 37, 66; [4c] M. He, S. Haswell, P. Fletcher, Lab Chip , 4, 38; B. Ondruschka, W. Bonrath, A. Gun, Green Chem. Fletcher, Appl. A , [4d] B. Strauss, Acc. Fletcher, Sen. De La Hoz, A. Diaz-Ortiz, A. Moreno, Chem.

Ultrasound and microwaves : recent advances in organic chemistry

Actuators, B , , Perreux, A. Loupy, Tetrahedron , 57, [20] For a literature survey on commercially available microwave ; [5c] N. Kuhnert, Angew. See also [5d] C. Strauss, Angew. Bogdal, P. Penczek, J. Pielichowski, A. Prociak, Adv. Wiesbrock, R. Hoogenboom, ge. Schubert, Macromol. Milestone s. Larhed, A.

Table of Contents

Hallberg, Drug Discovery Today , 6, ; [21] R. Jachuck, D. Selvaraj, R. Varma, Green Chem. Wathey, J. Tierney, P. Westman, Drug Discovery Today , 7, ; [7c] F. Al-Obeidi, R. Austin, [22] [22a] E. Comer, M. Organ, J. Okonya, D. Bond, Mini-Rev. Shore, S. Morin, M. Organ, Angew. Shipe, S. Wolkenberg, C. Lindsley, Drug , 45, ; [22c] E. Organ, Chem. Kappe, 11, Dallinger, Nat. Drug Discovery , 5, Kunz, A.

Kirschning, H. Wen, W. Solodenko, [8] [8a] S. Barlow, S. Marder, Adv. Cecilia, C. Kappe, T. Turek, Catal. Today , , [8b] Y.

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Chemistry World. Education in Chemistry. Open Access. Historical Collection. You do not have JavaScript enabled. Please enable JavaScript to access the full features of the site or access our non-JavaScript page. Issue 1, Previous Article Next Article. This article is part of the themed collection: Enabling Technologies for Organic Synthesis.

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