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Snyder, S. A.: 2016 Science of Synthesis, 2015/4a: Applications of Domino Transformations in Organic Synthesis 1 DOI: 10.1055/sos-SD-219-00200
Applications of Domino Transformations in Organic Synthesis 1

1.5.3 Brook Rearrangement as the Key Step in Domino Reactions

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Book

Editor: Snyder, S. A.

Authors: Adu-Ampratwum, D.; Anderson, E.; Armbrust, K. W.; Devery, J.; Douglas, J.; Doyle, M. P.; Engle, K. M.; Forsyth, C. J.; Gille, F.; Halkina, T.; Hu, X.; Jamison, T.; Kelley, E. H.; Kirschning, A.; Lee, D.; Maimone, T.; Merino, E.; Nevado Blazquez, C.; O'Connor, M. J.; Ohshima, T.; Parker, K.; Renata, H.; Salvador, A.; Schaumann, E.; Shenvi, R.; Shi, L.-L.; Sittihan, S.; Snyder, S. A.; Stephenson, C. R. J.; Tang, M.; Truong, P.; Tu, Y.-Q.; Wan, K.; Wang, S.-H.; Wolling, M.; Xu, X.; Yang, Z.

Title: Applications of Domino Transformations in Organic Synthesis 1

Print ISBN: 9783131731319; Online ISBN: 9783132402522; Book DOI: 10.1055/b-003-128286

1st edition © 2016. Thieme. All rights reserved.
Georg Thieme Verlag KG, Stuttgart

Subjects: Organic Chemistry;Chemical Reactions, Catalysis;Organometallic Chemistry;Laboratory Techniques, Stoichiometry

Science of Synthesis Reference Libraries



Parent publication

Title: Science of Synthesis

DOI: 10.1055/b-00000101

Series Editors: Carreira, E. M.; Decicco, C. P.; Fürstner, A.; Koch, G.; Molander, G.; Schaumann, E.; Shibasaki, M.; Thomas, E. J.; Trost, B. M.

Type: Multivolume Edition

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Abstract

The Brook rearrangement has lost its Cinderella status over the past twenty years since being embedded into cascade reaction sequences. The powerful formation of carbanions through silyl migration has been exploited for the development of many new methodologies and has been used as a key transformation in complex natural product syntheses. Now, the Brook rearrangement belongs to the common repertoire of synthetic organic chemists.

Key words

Brook rearrangement - domino reactions - migration - organosilicon chemistry - total synthesis
 
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