Corrigendum to "Asymmetric reduction using (R)-MeCBS and determination of absolute configuration of para-substituted 2-fluoroarylethanols" [Tetrahedron: Asymmetry 2008, 19, 1941-1946] (DOI:10.1016/j.tetasy.2008.07.019);Asymmetric reduction using (R)-MeCBS and determination of absolute configuration of para-substituted 2-fluoroarylethanols

Tetrahedron Asymmetry

Volumn 19, Issue 16, 2008, Pages 1941-1946

  Fuglseth, Erik ^a   Sundby, Eirik ^a   Bruheim, Per ^a,b   Hoff, Bård Helge ^a  

^a NORWEGIAN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Norway)

^b SINTEF MATERIALS AND CHEMISTRY   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

1 (4 (BENZYLOXY)PHENYL) 2 FLUOROETHANOL; 1 (4 BROMOPHENYL) 2 FLUOROETHANOL; 2 FLUORO 1 (4 (TRIFLUOROMETHYL)PHENYL)ETHANOL; 2 FLUORO 1 (4 FLUOROPHENYL)ETHANOL; 2 FLUORO 1 (4 METHOXYPHENYL)ETHANOL; 2 FLUORO 1 (4 NITROPHENYL)ETHANOL; 2 FLUORO 1 ARYLETHANOL DERIVATIVE; 2 FLUORO 1 HYDROXYETHYL)BENZONITRILE; 2 FLUORO 1 PHENYLETHANOL; ACETOPHENONE DERIVATIVE; ALCOHOL DERIVATIVE; ALPHA FLUOROACETOPHENONE DERIVATIVE; BENZOIC ACID DERIVATIVE; DICHLOROMETHANE; ETHER; ETHYLENE GLYCOL DIMETHYL ETHER; METHANE; METHYL OXAZABOROLIDINE; OXAZABOROLIDINE DERIVATIVE; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHIRALITY; CIRCULAR DICHROISM; ENANTIOMER; ENANTIOSELECTIVITY; PRIORITY JOURNAL; REDUCTION; SUBSTITUTION REACTION;

EID: 50649093988     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2009.02.002     Document Type: Erratum

References (40)

1. Begue J.P., and Bonnet-Delpon D. J. Fluorine Chem. 127 (2006) 992-1012
2. Kirk K.L. J. Fluorine Chem. 127 (2006) 1013-1029
3. Kirsch P., and Bremer M. Angew. Chem., Int. Ed. 39 (2000) 4216-4235
4. Shimizu M., and Hiyama T. Angew. Chem., Int. Ed. 44 (2005) 214-231
5. Thayer A.M. Chem. Eng. News 84 (2006) 15-24 and 27-32
6. Brown, A. D.; Bunnage, M. E.; Butcher, K. J.; Glossop, P. A.; James, K.; Lane, C. A. L.; Lewthwaite, R. A.; Price, D. A. WO 2005092841, 2005.
7. Gauthier, J. Y.; Li, C. S.; Mellon, C. U.S. 2006111440, 2005.
8. Navari R.M. Expert Rev. Anticancer Ther. 4 (2004) 715-724
9. Renaudet O., and Reymond J.L. Org. Lett. 6 (2004) 397-400
10. Barkakaty B., Takaguchi Y., and Tsuboi S. Tetrahedron 63 (2006) 970-976
11. Matsuda T., Harada T., and Nakamura K. Chem. Commun. (2000) 1367-1368
12. Nakamura K., and Yamanaka R. Tetrahedron: Asymmetry 13 (2002) 2529-2533
13. Wei Z.L., Li Z.Y., and Lin G.Q. Tetrahedron 54 (1998) 13059-13072
14. Ramachandran P.V., Teodorovic A.V., Gong G., and Brown H.C. Tetrahedron: Asymmetry 5 (1994) 1075-1086
15. Haufe G., Bruns S., and Runge M. J. Fluorine Chem. 112 (2001) 55-61
16. Haufe G., and Bruns S. Adv. Synth. Catal. 344 (2002) 165-171
17. Gais H.J., Jungen M., and Jadhav V. J. Org. Chem. 66 (2001) 3384-3396
18. Kitazume T., Asai M., Lin J.T., and Yamazaki T. J. Fluorine Chem. 35 (1987) 477-488
19. Lin J.T., Asai M., Ohnogi T., Yamazaki T., and Kitazume T. Chem. Express 2 (1987) 293-296
20. Corey E.J., Bakshi R.K., and Shibata S. J. Am. Chem. Soc. 109 (1987) 5551-5553
21. Mathre D.J., Thompson A.S., Douglas A.W., Hoogsteen K., Carroll J.D., Corley E.G., and Grabowski E.J.J. J. Org. Chem. 58 (1993) 2880-2888
22. Hoogenraad M., Klaus G.M., Elders N., Hooijschuur S.M., McKay B., Smith A.A., and Damen E.W.P. Tetrahedron: Asymmetry 15 (2004) 519-523
23. Gilmore N.J., and Jones S. Tetrahedron: Asymmetry 14 (2003) 2115-2118
24. Xu J., Wei T., and Zhang Q. J. Org. Chem 68 (2003) 10146-10151
25. Corey E.J., and Helal C.J. Tetrahedron Lett. 36 (1995) 9153-9156
26. Xu J., Wei T., and Zhang Q. J. Org. Chem. 69 (2004) 6860-6866
27. Nevalainen V. Tetrahedron: Asymmetry 2 (1991) 827-842
28. Nevalainen V. Tetrahedron: Asymmetry 3 (1992) 933-945
29. Hirao H., and Fujimoto H. J. Phys. Chem. A 104 (2000) 6649-6655
30. Alagona G., Ghio C., Persico M., and Tomasi S. J. Am. Chem. Soc. 125 (2003) 10027-10039
31. Brodfuehrer P.R., Smith P., Dillon J.L., and Vemishetti P. Org. Process Res. Dev. 1 (1997) 176-178
32. Yanagi T., Kikuchi K., Takeuchi H., Ishikawa T., Nishimura T., Kubota M., and Yamamoto I. Chem. Pharm. Bull. 51 (2003) 221-223
33. Bervova N., and Nakanishi K. Circular dichroism. Principles and Applications. In: Berova N., Nakanishi K., and Woody R.W. (Eds). Exciton Chirality Method: Principles and Applications (2000), Wiley-VCH, New York 337-382
34. Harada N., and Nakanishi K. Circular Dichroism Spectroscopy. Exciton Coupling in Organic Stereochemistry (1983), University Science Books, Mill Valley pp 1-460
35. Adam W., Lukacs Z., Viebach K., Humpf H.U., Saha-Moeller C.R., and Schreier P. J. Org. Chem. 65 (2000) 186-190
36. Anderson E.M., Larsson K.M., and Kirk O. Biocatal. Biotransform. 16 (1998) 181-204
37. Orrenius C., Haeffner F., Rotticci D., Ohrner N., Norin T., and Hult K. Biocatal. Biotransform. 16 (1998) 1-15
38. Berova N., Di Bari L., and Pescitelli G. Chem. Soc. Rev. 36 (2007) 914-931
39. Fuglseth E., Krane Thvedt T.H., Førde Møll M., and Hoff B.H. Tetrahedron 64 (2008) 7318-7323
40. Rakels J.L.L., Straathof A.J.J., and Heijnen J.J. Enzyme Microb. Technol. 15 (1993) 1051-1056