Catalytic enantioselective reactions part 7. Synthesis of new β-aminoalcohols derived from α-D-glucose as chiral catalysts for the catalytic enantioselective addition of diethylzinc to aldehydes

Synthetic Communications

Volumn 26, Issue 5, 1996, Pages 855-865

  Cho, Byung Tae ^a   Kim, Namdu ^a  

^a Hallym University   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

AMINOALCOHOL; CARBOHYDRATE DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; ENANTIOMER; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0029943122     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1080/00397919608003689     Document Type: Article

References (11)

1. For reviews, see (a) Soai, K. ; Niwa, S. Chem. Rev. 1992, 92, 833 and references cited therein; (b) Noyori, R. ; Kuamura, M. Angew. Chem. Int. Ed. Eng. 1991, 30, 49; (c) Noyori, R. ; Kitamura, M. 'Modern Synthetic Methods' ed. R. Scheffold, Springer-Verlag, 1989, pp 115 - 198.
2. For reviews, see (a) Soai, K. ; Niwa, S. Chem. Rev. 1992, 92, 833 and references cited therein; (b) Noyori, R. ; Kuamura, M. Angew. Chem. Int. Ed. Eng. 1991, 30, 49; (c) Noyori, R. ; Kitamura, M. 'Modern Synthetic Methods' ed. R. Scheffold, Springer-Verlag, 1989, pp 115 - 198.
3. For reviews, see (a) Soai, K. ; Niwa, S. Chem. Rev. 1992, 92, 833 and references cited therein; (b) Noyori, R. ; Kuamura, M. Angew. Chem. Int. Ed. Eng. 1991, 30, 49; (c) Noyori, R. ; Kitamura, M. 'Modern Synthetic Methods' ed. R. Scheffold, Springer-Verlag, 1989, pp 115 - 198.
4. (a) Cho, B. T. ; Kim, N. Tetrahedron Lett. 1994, 35, 4115;
5. (b) Cho, B. T. ; Kim, N. Bull. Korean Chem. Soc. 1994, 15, 931;
6. (c) Cho, B. T. ; Kim, N. Synth.Commun. 1995, 25, 167.
7. Schmidt, O. Th. 'Methods in Carbohydrate Chemistry ', ed. Whistler, R. L. ; Wolfrom, R. L., vol. 2. Academic Press, 1963, pp 320.
8. Muskat, T. E. J. Am. Chem. Soc. 1934, 56, 2449.
9. Org. Synth. Col. VII. 139.
10. Szabo', P. ; Szabo', L. J. Chem. Soc. 1964, 5139.
11. Dale, J. A ; Dull, D. L. ; Mosher, H. S. J. Org. Chem. 1969, 34, 2543. MTPA = α-methoxy-α-(trifluoromethyl)phenylacetic acid.