Literature DB >> 20041458

Beyond traditional cross couplings: the scope of the cross dehydrogenative coupling reaction.

Caroline J Scheuermann1.   

Abstract

The development of new and environmentally compatible methods for the synthesis of C-C and C-heteroatom bonds is of great significance to researchers. The cross dehydrogenative coupling (CDC) is emerging as an important tool for chemists with a variety of, often inexpensive, metal catalysts able to perform these reactions both regio- and enantioselectively. Perhaps more importantly CDC methodology has been shown to be extremely environmentally friendly and facile being able to be carried out in aqueous environments under an atmosphere of air. This Focus Review intends to give an overview of the most contemporary developments in this exciting and emerging area of cross-coupling chemistry.

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Year:  2010        PMID: 20041458     DOI: 10.1002/asia.200900487

Source DB:  PubMed          Journal:  Chem Asian J        ISSN: 1861-471X


  31 in total

1.  Asymmetric cross-dehydrogenative coupling enabled by the design and application of chiral triazole-containing phosphoric acids.

Authors:  Andrew J Neel; Jörg P Hehn; Pascal F Tripet; F Dean Toste
Journal:  J Am Chem Soc       Date:  2013-09-11       Impact factor: 15.419

2.  A General and Practical Palladium-Catalyzed Direct α-Arylation of Amides with Aryl Halides.

Authors:  Bing Zheng; Tiezheng Jia; Patrick J Walsh
Journal:  Adv Synth Catal       Date:  2014-01-13       Impact factor: 5.837

3.  Palladium-catalyzed acid-free Fujiwara-Moritani alkenylation of 4-thiazolidinones.

Authors:  Anuj Patel; Janki Patel; Kishor H Chikhalia
Journal:  Mol Divers       Date:  2017-06-15       Impact factor: 2.943

4.  A facile, metal- and solvent-free, autoxidative coupling of quinolines with indoles and pyrroles.

Authors:  Mikaël Brasse; Jonathan A Ellman; Robert G Bergman
Journal:  Chem Commun (Camb)       Date:  2011-03-29       Impact factor: 6.222

5.  Transforming Olefins into γ,δ-Unsaturated Nitriles through Copper Catalysis.

Authors:  Xuesong Wu; Jan Riedel; Vy M Dong
Journal:  Angew Chem Int Ed Engl       Date:  2017-08-10       Impact factor: 15.336

6.  Palladium(II)-catalyzed dehydrogenative alkenylation of cyclic enaminones via the Fujiwara-Moritani reaction.

Authors:  Yi-Yun Yu; Micah J Niphakis; Gunda I Georg
Journal:  Org Lett       Date:  2011-10-13       Impact factor: 6.005

7.  Dehydrogenative alkenylation of uracils via palladium-catalyzed regioselective C-H activation.

Authors:  Yi-Yun Yu; Gunda I Georg
Journal:  Chem Commun (Camb)       Date:  2013-03-25       Impact factor: 6.222

8.  Metal-free C(sp(3))-H functionalization: oxidative carbo-oxygenation of α-diazo carbonyls via radical dediazotization.

Authors:  Nan-Nan Wang; Wen-Juan Hao; Tian-Shu Zhang; Guigen Li; Ya-Nan Wu; Shu-Jiang Tu; Bo Jiang
Journal:  Chem Commun (Camb)       Date:  2016-03-21       Impact factor: 6.222

9.  Copper-catalyzed oxidative cross-dehydrogenative coupling of 2H-chromenes and terminal alkynes.

Authors:  Fei Yang; Yangshan Li; Paul E Floreancig; Xiaoyan Li; Lei Liu
Journal:  Org Biomol Chem       Date:  2018-07-18       Impact factor: 3.876

10.  Cross-dehydrogenative coupling and oxidative-amination reactions of ethers and alcohols with aromatics and heteroaromatics.

Authors:  Mahesh K Lakshman; Prasanna K Vuram
Journal:  Chem Sci       Date:  2017-06-30       Impact factor: 9.825

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