stereoselective intramolecular 1,3-dipolar nitrile oxide cycloaddition reaction of...

1
2007 Isoxazole derivatives R 0240 Stereoselective Intramolecular 1,3-Dipolar Nitrile Oxide Cycloaddition Reaction of N-Formyl-β-nitroamides. — Starting from readily available nitroalkanes and form- amides, a new two-step stereoselective synthesis of bicyclic-4,5-dihydroisoxazoles is developed. The products are useful synthons in aza-heterocyclic chemistry. — (KADOWAKI, A.; NAGATA, Y.; UNO, H.; KAMIMURA*, A.; Tetrahedron Lett. 48 (2007) 10, 1823-1825; Dep. Appl. Mol. Biosci., Grad. Sch. Med., Yamaguchi Univ., Ube, Yamaguchi 755, Japan; Eng.) — Mais 25- 123

Upload: ayako-kadowaki

Post on 11-Jun-2016

219 views

Category:

Documents


0 download

TRANSCRIPT

Page 1: Stereoselective Intramolecular 1,3-Dipolar Nitrile Oxide Cycloaddition Reaction of N-Formyl-β-nitroamides

2007

Isoxazole derivativesR 0240 Stereoselective Intramolecular 1,3-Dipolar Nitrile Oxide Cycloaddition Reaction

of N-Formyl-β-nitroamides. — Starting from readily available nitroalkanes and form-amides, a new two-step stereoselective synthesis of bicyclic-4,5-dihydroisoxazoles is developed. The products are useful synthons in aza-heterocyclic chemistry. — (KADOWAKI, A.; NAGATA, Y.; UNO, H.; KAMIMURA*, A.; Tetrahedron Lett. 48 (2007) 10, 1823-1825; Dep. Appl. Mol. Biosci., Grad. Sch. Med., Yamaguchi Univ., Ube, Yamaguchi 755, Japan; Eng.) — Mais

25- 123