An iodine-promoted, mild and efficient method for the synthesis of phenols from arylboronic acids

Synlett

Volumn 23, Issue 7, 2012, Pages 1079-1081

  Gogoi, Ankur ^a   Bora, Utpal ^a  

^a DIBRUGARH UNIVERSITY   (India)

Author keywords

arylboronic acid; hydrogen peroxide; hydroxylation; iodine; phenol

Indexed keywords

ARYLBORONIC ACID DERIVATIVE; BORONIC ACID DERIVATIVE; HYDROGEN PEROXIDE; IODINE; PHENOL DERIVATIVE; UNCLASSIFIED DRUG;

AQUEOUS SOLUTION; CATALYSIS; HYDROXYLATION; REACTION TIME; REVIEW; ROOM TEMPERATURE; SYNTHESIS;

EID: 84859817112     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0031-1290654     Document Type: Review

References (33)

1. Tyman J H. P., Synthetic and Natural Phenols Elsevier New York 1996
2. Rappoport Z, The Chemistry of Phenols Wiley-VCH Weinheim 2003
3. Fyfe C A., In The Chemistry of the Hydroxyl Group Vol. 1 Patai S Wiley Interscience New York 1971 83-127
4. Hoarau C, Pettus T R. R., Synlett 2003 127
5. Hanson P, Jones J R., Taylor A B., Walton P H., Timms A W., J. Chem. Soc., Perkin Trans. 2 2002 1135
6. George T, Mabon R, Sweeney G, Sweeney B J., Tavassoli A, J. Chem. Soc., Perkin Trans. 1 2000 2529; and reference cited therein
7. Thakur K G., Sekar G, Chem. Commun. 2011 47 6692
8. Mehmood A, Leadbeater N E., Catal. Commun. 2010 12 64
9. Anderson K W., Ikawa T, Tundel R E., Buchwald S L., J. Am. Chem. Soc. 2006 128 10694
10. Schulz T, Torborg C, Schaffner B, Huang J, Zapf A, Kadyrov R, Borner A, Beller M, Angew. Chem. Int. Ed. 2009 48 918
11. Sergeev A G., Schulz T, Torborg C, Spannenberg A, Neumann H, Beller M, Angew. Chem. Int. Ed. 2009 48 7595
12. Willis M C., Angew. Chem. Int. Ed. 2007 46 3402
13. Kwong F Y., Chen G, Chan A S. C., Tetrahedron Lett. 2007 48 473
14. Gallon B J., Kojima R W., Kaner R B., Diaconescu P L., Angew. Chem. Int. Ed. 2007 46 7251
15. Zhao D, Wu N, Zhang S, Xi P, Su X, Lan J, You J, Angew. Chem. Int. Ed. 2009 48 8729
16. Tlili A, Xia N, Monnier F, Taillefer M, Angew. Chem. Int. Ed. 2009 48 8725
17. Matteson D S., Tetrahedron 1989 45 1859
18. Pelter A, Smith K, Brown H C., Borane Reagents Academic Press New York 1988
19. Sakurai H, Tsunoyama H, Tsunoyama H, Tsukuda T, J. Organomet. Chem. 2007 692 368
20. Lam P Y. S., Bonne D, Vincent G, Clark C G., Combs A P., Tetrahedron Lett. 2003 44 1691
21. Jung Y C., Mishra R K., Yoon C H., Jung K W., Org. Lett. 2003 5 2231
22. Xu J, Wang X, Shao C, Su D, Cheng G, Hu Y, Org. Lett. 2010 12 1964
23. Surya Prakash G K., Chacko S, Panja C, Thomas T E., Gurung L, Rasul G, Mathew T, Olah G A., Adv. Synth. Catal. 2009 351 1567
24. Kianmehr E, Yahyaee M, Tabatabai K, Tetrahedron Lett. 2007 48 2713
25. Webb K S., Levy D, Tetrahedron Lett. 1995 36 5117
26. Simon J, Salzbrunn S, Surya Prakash G K., Petasis N A., Olah G A., J. Org. Chem. 2001 66 633
27. Piera J, Backvall J.-E, Angew. Chem. Int. Ed. 2008 47 3506
28. Jereb M, Vrazic D, Zupan M, Tetrahedron 2011 67 1355
29. Das S, Borah R, Devi R R., Thakur A J., Synlett 2008 2741
30. Kuivila H G., J. Am. Chem. Soc. 1954 76 870
31. Kuivila H G., Armour A G., J. Am. Chem. Soc. 1957 79 5659
32. Filipan-Litvic M, Litvic M, Vinkovic V, Tetrahedron 2008 64 5649
33. Zaugg H E., Schaefer A D., J. Am. Chem. Soc. 1965 87 1857