Effect of the nature and position of the chiral auxiliary on stere-oselective synthesis of oxazolines.-Reference-Cited by-同舟云学术

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Effect of the nature and position of the chiral auxiliary on stere-oselective synthesis of oxazolines.

Published:1994-06 Issue:2 Volume:5 Page:135-144
ISSN:1120-6349
Container-title:Rendiconti Lincei
language:en
Short-container-title:Rend. Fis. Acc. Lincei

Author:

Colonna Stefano,Manfredi Amedea,Solladié-Cavallo Arlette,Quazzotti Serge,Fischer Jean,De Cian André

Publisher

Springer Science and Business Media LLC

Subject

General Earth and Planetary Sciences,General Agricultural and Biological Sciences,General Environmental Science

Link

http://link.springer.com/content/pdf/10.1007/BF03001613.pdf

Reference16 articles.

1. Ito Y., Sawamura M., 1986.Catalytic asymmetric aldol reaction: reaction of aldehydes with isocyanoacetate catalyzed by a chiral ferrocenylphosphine-gold (I) complex. J. Am. Chem. Soc., 108: 6405–6406.

2. Ito Y., Sawamura M., Hayashi T., 1987.Asymmetric aldol reaction of an isocyanoacetate with aldehydes catalyzed by chiral ferrocenylphosphine-gold(I) complexes: design and preparation of new efficient ferrocenylphosphine ligands. Tetrahedron Lett., 28: 6215–6218.

3. Ito Y., Sawamura M., Shirakawa E., Hayashizaky K., Hayashi T., 1988.Asymmetric aldol reaction of α- lsocyanocarboxylates with paraformaldehyde catalyzed by chiral ferrocenylphosphine-gold(I) complexes: catalytic asymmetric synthesis of α-alkylsennes. Tetrahedron Let:., 29: 235–238.

4. Pastor S. D., Togni A., 1989.Asymmetric synthesis with chiral ferroceny lamine ligands: the importance of central chirality. J. Am. Chem. Soc, 111: 2333–2334.

5. Rawson D. J., Meyers A. L., 1991.Asymmetric tandem additions to chiral naphthyloxazolines. A new potent chiral auxiliary resulting in a major improvement in convenience and efficiency. J. Org. Chem., 56: 2292–2294.

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