Boric acid mediated N-acylation of sulfoximines

Synlett

Volumn , Issue 3, 2011, Pages 361-364

  Garimallaprabhakaran, Aswinkumar ^a   Harmata, Michael ^a  

^a UNIVERSITY OF MISSOURI   (United States)

Author keywords

acylation; amidation; boric acid; boronic acid; sulfoximine

Indexed keywords

ACETIC ACID; AROMATIC CARBOXYLIC ACID; BORIC ACID; BORONIC ACID DERIVATIVE; CARBOXYLIC ACID; INORGANIC ACID; SULFOXIMINE DERIVATIVE; UNCLASSIFIED DRUG;

ACYLATION; AMIDATION; ARTICLE; BIOCATALYST; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; LOADING TEST; N ACYLATION; NUCLEOPHILICITY; PHYSICAL CHEMISTRY; PROCESS OPTIMIZATION; PROTON NUCLEAR MAGNETIC RESONANCE; TEMPERATURE SENSITIVITY;

EID: 79551689080     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0030-1259328     Document Type: Article

References (27)

1. Worch C, Mayer A C., Bolm C, Synthesis and Use of Chiral Sulfoximines, In Organosulfur Chemistry in Asymmetric Synthesis Toru T Bolm C Wiley-VCH Weinheim 2008 209-229
2. Okamura H, Bolm C, Chem. Lett. 2004 33 482
3. Harmata M, Chemtracts 2003 16 660
4. Reggelin M, Zur C, Synthesis 2000 1
5. Harmata M, Rayanil K.-O, Espejo V R., Barnes C L., J. Org. Chem. 2009 74 3214
6. Harmata M, Cai Z, Chen Y, J. Org. Chem. 2009 74 5559
7. Harmata M, Huang C, Chen Y, Zheng P, Gao X, Ying W, Synlett 2008 2051
8. Harmata M, Rayanil K.-O, Gomes M G., Zheng P, Calkins N L., Kim S.-Y, Fan Y, Bumbu V, Lee D R., Wacharasindhu S, Hong X, Org. Lett. 2005 7 143
9. Harmata M, Hong X, Org. Lett. 2005 7 3581
10. Harmata M, Hong X, J. Am. Chem. Soc. 2003 125 5754
11. Harmata M, Pavri N, Angew. Chem. Int. Ed. 1999 38 2419
12. Harmata M, Claassen R J. III, Tetrahedron Lett. 1991 32 6497
13. Harmata M, Tetrahedron Lett. 1989 30 437
14. Hwang K J., Logusch E W., Tetrahedron Lett. 1987 28 4149
15. Bolm C, Hackenberger C P. R., Simic O, Verrucci M, Mller D, Bienewald F, Synthesis 2002 879
16. Bolm C, Mller D, Dalhoff C, Hackenberger C P. R., Weinhold E, Bioorg. Med. Chem. Lett. 2003 13 3207
17. Hackenberger C P. R., Raabe G, Bolm C, Chem. Eur. J. 2004 10 2942
18. Cho G Y., Okamura H, Bolm C, J. Org. Chem. 2005 70 2346
19. Barajas J G. H., Mendez L Y. V., Kouznetsov V V., Stashenko E E., Synthesis 2008 377
20. Maki T, Ishihara K, Yamamoto H, Tetrahedron 2007 63 8645
21. Arnold K, Davies B, Giles R L., Grosjean C, Smith G E., Whiting A, Adv. Synth. Catal. 2006 348 813
22. Tang P, Org. Synth. 2005 81 262
23. Latta R, Springsteen G, Wang B, Synthesis 2001 1611
24. Zoubi R M., Marion O, Hall D G., Angew. Chem. Int. Ed. 2008 47 2876
25. Ishihara K, Ohara S, Yamamoto H, Org. Synth. 2003 79 176
26. Brandt J, Gais H.-J, Tetrahedron: Asymmetry 1997 8 909
27. Marcelli T, Angew. Chem. Int. Ed. 2010 49 6840