Conversion of 1-alkenes into 1,4-diols through an auxiliary-mediated formal homoallylic C–H oxidation-Reference-Cited by-同舟云学术

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Conversion of 1-alkenes into 1,4-diols through an auxiliary-mediated formal homoallylic C–H oxidation

Published:2014-01-19 Issue:2 Volume:6 Page:122-125
ISSN:1755-4330
Container-title:Nature Chemistry
language:en
Short-container-title:Nature Chem

Author:

Ghavtadze Nugzar,Melkonyan Ferdinand S.,Gulevich Anton V.,Huang Chunhui,Gevorgyan Vladimir

Publisher

Springer Science and Business Media LLC

Subject

General Chemical Engineering,General Chemistry

Link

http://www.nature.com/articles/nchem.1841.pdf

Reference31 articles.

1. Yu, J-Q., Shi, Z. C–H Activation (Topics in Current Chemistry 292, Springer, 2010).

2. Engle, K. M., Mei, T-S., Wasa, M. & Yu, J-Q. Weak coordination as a powerful means for developing broadly useful C–H functionalization reactions. Acc. Chem. Res. 45, 788–802 (2011).

3. Wencel-Delord, J., Droge, T., Liu, F. & Glorius, F. Towards mild metal-catalyzed C–H bond activation. Chem. Soc. Rev. 40, 4740–4761 (2011).

4. Ackermann, L. Carboxylate-assisted transition-metal-catalyzed C–H bond functionalizations: mechanism and scope. Chem. Rev. 111, 1315–1345 (2011).

5. Lyons, T. W. & Sanford, M. S. Palladium-catalyzed ligand-directed C–H functionalization reactions. Chem. Rev. 110, 1147–1169 (2010).

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