A novel green protocol for ligand free Suzuki–Miyaura cross-coupling reactions in WEB at room temperature

Preeti Rekha Boruah; Abdul Aziz Ali; Bishwajit Saikia; Diganta Sarma

doi:10.1039/c4gc02522a

journal article Jan 01, 2015

A novel green protocol for ligand free Suzuki–Miyaura cross-coupling reactions in WEB at room temperature

Preeti Rekha Boruah Abdul Aziz Ali Bishwajit Saikia Diganta Sarma

Green Chem. Vol. 17 No. 3 pp. 1442-1445 · Royal Society of Chemistry (RSC)

View at Publisher Save 10.1039/c4gc02522a

Abstract

A highly efficient green protocol for palladium acetate-catalysed ligand-free Suzuki–Miyaura cross-coupling reactions in neat ‘water extract of banana (WEB)’ was developed. Suzuki–Miyaura reaction proceeds in WEB at very short reaction times under ‘ligand/external base/external promoters/organic medium’ free conditions.

Topics

No keywords indexed for this article. Browse by subject →

References

46

[1]

N. Miyaura , in Metal-Catalyzed Cross-Coupling Reactions, ed. de A. Meijere and F. Diederich, Wiley-VCH, New York, 2004, ch. 2

[2]

Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds

Norio. Miyaura, Akira. Suzuki

Chemical Reviews 1995 10.1021/cr00039a007

[3]

Nakamura Chem. Rev. (2004) 10.1021/cr020095i

[4]

Johansson Seechurn Angew. Chem. (2012) 10.1002/ange.201107017

[5]

Yin Chem. Rev. (2007) 10.1021/cr0505674

[6]

Littke Angew. Chem., Int. Ed. (2002) 10.1002/1521-3773(20021115)41:22<4176::aid-anie4176>3.0.co;2-u

[7]

Miura Angew. Chem., Int. Ed. (2004) 10.1002/anie.200301753

[8]

Wolf J. Org. Chem. (2008) 10.1021/jo701893m

[9]

Zim Org. Lett. (2001) 10.1021/ol016526l

[10]

Tobisu J. Am. Chem. Soc. (2011) 10.1021/ja207759e

[11]

González-Bobes J. Am. Chem. Soc. (2006) 10.1021/ja0613761

[12]

Thathagar J. Am. Chem. Soc. (2002) 10.1021/ja027716+

[13]

Homogeneous Catalysis with Metal Phosphine Complexes, ed. L. H. Pignolet, Plenum, New York, 1983

[14]

Beletskaya Chem. Rev. (2000) 10.1021/cr9903048

[15]

G. W. Parshall and S.Ittel, Homogeneous Catalysis, J. Wiley and Sons, New York, 1992, vol. 65

[16]

Marziale Green Chem. (2011) 10.1039/c0gc00522c

[17]

Ros J. Org. Chem. (2012) 10.1021/jo300548z

[18]

Littke Angew. Chem., Int. Ed. (1998) 10.1002/(sici)1521-3773(19981231)37:24<3387::aid-anie3387>3.0.co;2-p

[19]

Wolfe J. Am. Chem. Soc. (1999) 10.1021/ja992130h

[20]

Stambuli Angew. Chem., Int. Ed. (2002) 10.1002/anie.200290036

[21]

Mathews J. Mol. Catal. A: Chem. (2003) 10.1016/s1381-1169(03)00447-3

[22]

Tang J. Organomet. Chem. (2013) 10.1016/j.jorganchem.2013.01.018

[23]

Rao Dalton Trans. (2012) 10.1039/c1dt11695a

[24]

Kim J. Org. Chem. (2005) 10.1021/jo050721m

[25]

John Dalton Trans. (2010) 10.1039/c002475a

[26]

Li Organometallics (2008) 10.1021/om700949s

[27]

Alacid J. Organomet. Chem. (2009) 10.1016/j.jorganchem.2009.01.016

[28]

Corma Tetrahedron (2004) 10.1016/j.tet.2004.06.121

[29]

Mu Tetrahedron (2007) 10.1016/j.tet.2007.08.004

[30]

Decottignies Catal. Commun. (2013) 10.1016/j.catcom.2012.12.004

[31]

Polshettiwar ChemSusChem (2010) 10.1002/cssc.200900221

[32]

Polshettiwar Coord. Chem. Rev. (2009) 10.1016/j.ccr.2009.06.001

[33]

Hervé RSC Adv. (2014) 10.1039/c3ra47911k

[34]

Gallagher-Duval New J. Chem. (2013) 10.1039/c3nj00174a

[35]

Sartori Synthesis (2012)

[36]

Sartori Synthesis (2013)

[37]

Organic Synthesis in Water, ed. P. A. Greico, Blackie Academic & Professional, London, 1998

[38]

C. J. Li and T. H.Chen, Organic Reactions in Aqueous Media, Klewer Academic Publishers, Dordrecht, 1997

[39]

Saikia Tetrahedron Lett. (2015) 10.1016/j.tetlet.2014.12.061

[40]

Liu J. Org. Chem. (2006) 10.1021/jo060122v

[41]

Han Organometallics (2007) 10.1021/om7009107

[42]

Brendgen Eur. J. Org. Chem. (2006) 10.1002/ejoc.200500943

[43]

Sheloumov Eur. J. Inorg. Chem. (2008) 10.1002/ejic.200700923

[44]

Mondal Green Chem. (2012) 10.1039/c2gc35401b

[45]

Boruah Tetrahedron Lett. (2014) 10.1016/j.tetlet.2014.02.126

[46]

Deka Indian J. Tradit. Know. (2007)

Cited By

145

Fabrication of Cu/Cu2O nanoparticles by banana peel extract for 4-nitrophenol degradation

Jose-Luis Ortiz-Quiñonez, Leonardo Dante Pérez Pérez · 2026

Chemical Engineering Journal Advanc...

Metrics

145

Citations

46

References

Details

Published: Jan 01, 2015
Vol/Issue: 17(3)
Pages: 1442-1445

Authors

P

Preeti Rekha Boruah

Department of Chemistry; Dibrugarh University; Dibrugarh-786004; India

A

Abdul Aziz Ali

Department of Chemistry; Dibrugarh University; Dibrugarh-786004; India

B

Bishwajit Saikia

Department of Chemistry; Dibrugarh University; Dibrugarh-786004; India

D

Diganta Sarma

Department of Chemistry; Dibrugarh University; Dibrugarh-786004; India

Cite This Article

Preeti Rekha Boruah, Abdul Aziz Ali, Bishwajit Saikia, et al. (2015). A novel green protocol for ligand free Suzuki–Miyaura cross-coupling reactions in WEB at room temperature. Green Chem., 17(3), 1442-1445. https://doi.org/10.1039/c4gc02522a

A novel green protocol for ligand free Suzuki–Miyaura cross-coupling reactions in WEB at room temperature

You May Also Like