Synthesis of a Schiff's base chiral ligand with a trifluoromethyl carbinol moiety

Tetrahedron Asymmetry

Volumn 17, Issue 18, 2006, Pages 2654-2658

  Sokeirik, Yasser Samir ^a   Omote, Masaaki ^a   Sato, Kazuyuki ^a   Kumadaki, Itsumaro ^a   Ando, Akira ^a  

^a Setsunan University   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE DERIVATIVE; DIETHYLZINC; METHANOL DERIVATIVE; SCHIFF BASE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHIRALITY; GAS CHROMATOGRAPHY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; SYNTHESIS;

EID: 33750501985     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2006.08.023     Document Type: Article

References (16)

1. For review, see:. Katsuki T. Chem. Soc. Rev. 33 (2004) 437-444
2. Omote M., Kominato A., Sugawara M., Sato K., Ando A., and Kumadaki I. Tetrahedron Lett. 40 (1999) 5583-5585
3. 3 group, see:. Kumadaki I. Rev. Heteroatom. Chem. 9 (1993) 181
4. Meyers A.I. Tetrahedron Lett. 29 (1988) 5617-5620
5. Kriis K., Kanger T., Müürisepp A., and Lopp M. Tetrahedron: Asymmetry 14 (2003) 2271-2275
6. Bauer T., and Gajewiak J. Tetrahedron: Asymmetry 16 (2005) 851-855
7. Huan W., Hu Q., and Pu L. J. Org. Chem. 64 (1999) 7940-7956
8. Vaestilae P., Pastor I.M., and Adolfsson H. J. Org. Chem. 70 (2005) 2921-2929
9. Priego J., Mancheño O.G., Cabrera S., and Carretero J.C. Chem. Commun. (2001) 2026-2027
10. Cozzi P.G., Papa A., and Umani-Ronchi A. Tetrahedron Lett. 37 (1996) 4613-4616
11. Kitamura M., Suga S., Niwa M., and Noyori R. J. Am. Chem. Soc. 117 (1995) 4832-4842
12. Kitamura M., Yamakawa M., Oka H., Suga S., and Noyori R. Chem. Eur. J. 2 (1996) 1171-1181
13. Kitamura M., Suga S., Makoto N., Noyori R., Zhai Z.-X., and Suga H. J. Phys. Chem. 98 (1994) 12776-12781
14. Kitamura M., Oka H., Suga S., and Noyori R. J. Am. Chem. Soc. 120 (1998) 9800-9809
15. Katagiri T., Fujiwara Y., Takahashi S., Ozaki N., and Uneyama K. Chem. Commun. (2002) 986-987
16. This complex was not formed when either half or 1 equiv of diethylzinc was used. It only formed in the presence of a large excess of diethylzinc.