Fluoride-catalyzed aldol-type reactions of α-isocyano esters producing 2-oxazoline derivatives

Heterocycles

Volumn 52, Issue 1, 2000, Pages 91-93

  Ito, Yoshihiko ^a   Higuchi, Noriko ^a   Murakami, Masahiro ^a  

^a KYOTO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

FLUORIDE; NITRILE; OXAZOLINE DERIVATIVE;

ARTICLE; CATALYSIS; CYCLIZATION; DERIVATIZATION; DRUG SYNTHESIS; REACTION ANALYSIS; SIALYLATION; STOICHIOMETRY;

EID: 0033955155     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-99-s19     Document Type: Article

References (7)

1. This paper is dedicated to Professor Teruaki Mukaiyama for leading us by example in his uncompromising approach to organic synthesis.
2. For reviews: (a) U. Schöllkopf, Angew. Chem., Int. Ed. EngL., 1977, 16, 339.
3. (b) K. Matsumoto, T. Moriya, and M. Suzuki, J. Synth. Org. Chem., Jpn., 1985,43, 764.
4. M. Murakami, N. Higuchi, and Y. Ito, Chem. Express, 1990, 5, 411.
5. For the fluoride-catalyzed 1,4-addition of α-isocyano esters, see: M. Murakami, N. Hasegawa, I. Tomita, M. Inouye, and Y. Ito, Tetrahedron Lett., 1989, 30, 1257.
6. T. Mukaiyama, 'Organic Reactions,' Vol. 28, 1982, pp. 203-331.
7. I. Kuwajima and E. Nakamura, Acc. Chem. Res., 1985, 18, 181.