DABO boronates: Stable heterocyclic boronic acid complexes for use in suzuki-miyaura cross-coupling reactions

Synlett

Volumn , Issue 16, 2011, Pages 2392-2396

  Reilly, Maureen K ^a   Rychnovsky, Scott D ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

aryl boronate; cross coupling; heterocyclic boronate; palladium catalysis; Suzuki Miyaura reaction

Indexed keywords

2 FURYL DIETHANOLAMINE DERIVATIVE; 2 METHOXYPHENYL DIETHANOLAMINE DERIVATIVE; 4 BROMOANISOLE; BORONIC ACID DERIVATIVE; DIETHANOLAMINE BORONIC ACID DERIVATIVE; HETEROARYL DIETHANOLAMINE DERIVATIVE; PALLADIUM; PHENYL DIETHANOLAMINE DERIVATIVE; TERT BUTYL 2 (THIOPHEN 3 YL) 1H PYRROLE 1 CARBOXYLIC ACID; TRIFLUOROMETHANESULFONIC ACID VINYL ESTER; UNCLASSIFIED DRUG; VINYL DIETHANOLAMINE DERIVATIVE;

ARTICLE; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CROSS COUPLING REACTION; MIYAURA CROSS COUPLING REACTION; SUZUKI REACTION; SYNTHESIS;

EID: 80053052049     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0030-1261218     Document Type: Article

References (24)

1. Miyaura N, Suzuki A, Chem. Rev. 1995 95 2457
2. Nicolaou K C., Bulger P G., Sarlah D, Angew. Chem. Int. Ed. 2005 44 4442
3. Hayashi T, Yamasaki K, Chem. Rev. 2003 103 2829
4. Lin P.-S, Jeganmohan M, Cheng C.-H, Chem. Eur. J. 2008 14 11296
5. Hall D G., Boronic Acids Wiley-VCH Weinheim 2005
6. Billingsley K, Buchwald S L., J. Am. Chem. Soc. 2007 129 3358
7. Molander G A., Canturk B, Kennedy L E., J. Org. Chem. 2009 74 973
8. Molander G A., Bernardi C R., J. Org. Chem. 2002 67 8424
9. Molander G A., Sandrock D L., Curr. Opin. Drug Discovery Dev. 2009 12 811
10. Mancilla T, Contreras R, Wrackmeyer B, J. Organomet. Chem. 1986 307 1
11. Gillis E P., Burke M D., J. Am. Chem. Soc. 2007 129 6716
12. Knapp D M., Gillis E P., Burke M D., J. Am. Chem. Soc. 2009 131 6961
13. Alessi M, Larkin A L., Ogilvie K A., Green L A., Lai S, Lopez S, Snieckus V, J. Org. Chem. 2007 72 1588
14. Bouillon A, Lancelot J.-C, Santos J S., Callot V, Bovy P R., Rault S, Tetrahedron 2003 59 10043
15. Hodgson P B., Salingue F H., Tetrahedron Lett. 2004 45 685
16. Gros P, Doudouh A, Fort Y, Tetrahedron Lett. 2004 45 6239
17. Davies A G., Roberts B P., Ramsay W, J. Chem. Soc. B 1967 17
18. Letsinger R L., Skoog I, J. Am. Chem. Soc. 1955 77 2491
19. Crystallographic data:, Rettig S J., Trotter J, Can. J. Chem. 1975 53 1393
20. Caron S, Hawkins J M., J. Org. Chem. 1998 63 2054
21. Bonin H, Leuma-Yona R, Marchiori B, Demonchaux P, Gras E, Tetrahedron Lett. 2011 52 1132
22. Inoue M, Frontier A J., Danishefsky S J., Angew. Chem. Int. Ed. 2000 39 761
23. Wang Z, Elokdah H, McFarlane G, Pan S, Antane M, Tetrahedron Lett. 2006 47 3365
24. Molander G A., Yun C.-S, Tetrahedron 2002 58 1465