Download PDF
Aitken, R. A. et al.: 2016 Science of Synthesis, 2015/2: Knowledge Updates 2015/2 DOI: 10.1055/sos-SD-135-00077
Knowledge Updates 2015/2

35.2.1.1.8 Synthesis by Substitution of Hydrogen (Update 2015)

More Information

Book

Editors: Aitken, R. A.; Brønsted Nielsen, M.; Drabowicz, J.; Li, J. J.; Plietker, B.; Wirth, T.

Authors: Banert, K.; Brønsted Nielsen, M.; Cacciarini, M.; Elliott, M.; Grün, A.; Hagen, T.; Helgren, T.; Hennecke, U.; Iskra, J.; Kang, F.-A.; Keglevich, G.; Larsen, M. H.; Li, H.; Mazet, C.; Murphree, S.S.; Nomoto, A.; Ogawa, A.; Reißig, H.-U.; Saleh, B. A.; Singh, F. V. ; Tomé, A. C.; Wirth, T.; Yang, S.-M.; Zimmer, R.

Title: Knowledge Updates 2015/2

Print ISBN: 9783131984616; Online ISBN: 9783131975812; Book DOI: 10.1055/b-003-125870

1st Edition © 2016 Georg Thieme Verlag KG
Georg Thieme Verlag, Stuttgart

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

Science of Synthesis Knowledge Updates



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

Also available at
 

Abstract

This chapter is an update to the earlier Science of Synthesis contribution (Section 35.2.1.1) summarizing methodology for the bromination of non-activated C—H bonds, with a particular focus on regioselectivity.

Key words

bromination - halogenation - bromine compounds - halo compounds - bromides - halides - alkanes - carbon—halogen bonds
 
  • 1 Lorkovic I. M., Sun S., Gadewar S., Breed A., Macala G. S., Sardar A., Cross S. E., Sherman J. H., Stucky G. D., Ford P. C. J. Phys. Chem. A 2006; 110: 8695
  • 2 Schreiner P. R., Fokina N. A., Tkachenko B. A., Hausmann H., Serafin M., Dahl J. E. P., Liu S., Carlson R. M. K., Fokin A. A. J. Org. Chem. 2006; 71: 6709
  • 3 Fokin A. A., Schreiner P. R., Fokina N. A., Tkachenko B. A., Hausmann H., Serafin M., Dahl J. E. P., Liu S., Carlson R. M. K. J. Org. Chem. 2006; 71: 8532
  • 4 Jiang X., Shen M., Tang Y., Li C. Tetrahedron Lett. 2005; 46: 487
  • 5 Nishina Y., Morita J., Ohtani B. RSC Adv. 2013; 3: 2158
  • 6 Nishina Y., Hashimoto H., Kimura N., Miyata N., Fujii T., Ohtani B., Takada J. RSC Adv. 2012; 2: 6420
  • 7 Shaikh T. M., Sudalai A. Tetrahedron Lett. 2005; 46: 5589
  • 8 He Y., Goldsmith C. Synlett 2010; 1377
  • 9 Li Y., Ju J., Jia J., Sheng W., Han L., Gao J. Chin. J. Chem. 2010; 28: 2428
  • 10 Chen K., Richter J. M., Baran P. S. J. Am. Chem. Soc. 2008; 130: 7247
  • 11 Nishina Y., Ohtani B., Kikushima K. Beilstein J. Org. Chem. 2013; 9: 1663
  • 12 Kee C. W., Chan K. M., Wong M. W., Tan C.-H. Asian J. Org. Chem. 2014; 3: 536
  • 13 Sasano Y., Nishiyama T., Tomizawa M., Shibuya M., Iwabuchi Y. Heterocycles 2013; 87: 2109
  • 14 Fokin A. A., Schreiner P. R., Berger R., Robinson G. H., Wei P., Campana C. F. J. Am. Chem. Soc. 2006; 128: 5332
  • 15 Arbuj S. S., Waghmode S. B., Ramaswamy A. V. Tetrahedron Lett. 2007; 48: 1411
  • 16 Lowell A. N., Wall P. D., Waters S. P., Kozlowski M. C. Tetrahedron 2010; 66: 5573
  • 17 Beuille E., Darcos V., Coudane J., Lacroix-Desmazes P., Nottelet B. Macromol. React. Eng. 2014; 8: 141
  • 18 Friedrich J., Dörrich S., Berkefeld A., Kraft P., Tacke R. Organometallics 2014; 33: 796
  • 19 Shibatomi K., Zhang Y., Yamamoto H. Chem.–Asian J. 2008; 3: 1581
  • 20 Czifrák K., Szilágyi P., Somsák L. Tetrahedron: Asymmetry 2005; 16: 127
  • 21 Czifrák K., Somsák L. Carbohydr. Res. 2009; 344: 269
  • 22 Lee S. S., Greig I. R., Vocadlo D. J., McCarter J. D., Patrick B. O., Withers S. G. J. Am. Chem. Soc. 2011; 133: 15 826