Metal Bis(trifluoromethylsulfonyl)amides as Highly Efficient Lewis Acid Catalysts for Acylation Reactions

Synlett

Volumn 1996, Issue 2, 1996, Pages 171-172

  Mikami, Koichi ^a   Kotera, Osamu ^a   Motoyama, Yukihiro ^a   Sakaguchi, Hiroaki ^b   Maruta, Masamichi ^b  

^a TOKYO INSTITUTE OF TECHNOLOGY   (Japan)

^b CENTRAL GLASS CO LTD   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 1542485845     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1996-5363     Document Type: Article

References (14)

1. Reviews: D. Schinzer, Selectivities in Lewis Acid Promoted Reactions; Kluwer Academic Publishers: Dordrecht, 1989. S. Schambayati, S. L. Schreiber, In Comprehensive Organic Synthesis; B. M. Trost, I. Fleming, Eds.; Pergamon Press: Oxford 1991.
2. Reviews: D. Schinzer, Selectivities in Lewis Acid Promoted Reactions; Kluwer Academic Publishers: Dordrecht, 1989. S. Schambayati, S. L. Schreiber, In Comprehensive Organic Synthesis; B. M. Trost, I. Fleming, Eds.; Pergamon Press: Oxford 1991.
3. Reviews: H. Heaney, In Comprehensive Organic Synthesis; B. M. Trost, I. Fleming, Eds.; Pergamon Press: Oxford, 1991; Vol. 2, p. 733. G. A. Olah, Friedel-Crafts Chemistry; Wiley-Interscience: New York, 1973.
4. Reviews: H. Heaney, In Comprehensive Organic Synthesis; B. M. Trost, I. Fleming, Eds.; Pergamon Press: Oxford, 1991; Vol. 2, p. 733. G. A. Olah, Friedel-Crafts Chemistry; Wiley-Interscience: New York, 1973.
5. 3: J. Inanaga, Y. Sugimoto, T. Hanamoto, New J. Chem., 1995, 19, 707.
6. 3: J. Inanaga, Y. Sugimoto, T. Hanamoto, New J. Chem., 1995, 19, 707.
7. 3: J. Inanaga, Y. Sugimoto, T. Hanamoto, New J. Chem., 1995, 19, 707.
8. 3: J. Inanaga, Y. Sugimoto, T. Hanamoto, New J. Chem., 1995, 19, 707.
9. 3: J. Inanaga, Y. Sugimoto, T. Hanamoto, New J. Chem., 1995, 19, 707.
10. n, as catalysts for the Diels-Alder reactions: H. Kobayashi, J. Nie, T. Sonoda, Chem. Lett., 1995, 307. S. T. Handy, P. A. Grieco, C. Mineur, L. Ghosez, Synlett, 1995, 565.
11. n, as catalysts for the Diels-Alder reactions: H. Kobayashi, J. Nie, T. Sonoda, Chem. Lett., 1995, 307. S. T. Handy, P. A. Grieco, C. Mineur, L. Ghosez, Synlett, 1995, 565.
12. I. A. Koppel, R. W. Taft, F. Anvia, S.-Z. Zhu, L.-Q. Hu, K.-S. Sung, D. D. DesMarteau, L. M. Yagupolskii, Y. L. Yagupolskii, N. V. Ignat'ev, N. V. Kondratenko, A. Y. Volkonskii, V. M. Vlasov, R. Notario, P.-C. Maria, J. Am. Chem. Soc., 1994, 116, 3047.
13. 3 is prepared from ytterbium oxide and bis(trifluoromethylsulfonyl)imide in water.
14. 3 as a catalyst for acylation of alcohols in acetonitrile rather than in other organic solvents: K. Ishihara, M. Kubota, H. Kurihara, H. Yamamoto, J. Am. Chem. Soc., 1995, 117, 4413.