cheminform abstract: preparation of azetidines by 4-endo trig cyclizations of n-cinnamyl tosylamides

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2001 azetidine derivatives azetidine derivatives R 0045 04 - 120 Preparation of Azetidines by 4-endo trig Cyclizations of N-Cinnamyl Tosylamides. — Formation of azetidines via 4-endo cyclization of allylic amines is achieved. The reaction is proposed to proceed via a carbocation intermediate. — (ROBIN, SYLVIE; ROUSSEAU, GERARD; Eur. J. Org. Chem. (2000) 17, 3007-3011; Lab. Carbocycles, CNRS, Inst. Chim. Mol. Orsay, Univ. Paris-Sud, F-91405 Orsay, Fr.; EN) 1

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Page 1: ChemInform Abstract: Preparation of Azetidines by 4-endo trig Cyclizations of N-Cinnamyl Tosylamides

2001 azetidine derivatives

azetidine derivativesR 0045

04 - 120Preparation of Azetidines by 4-endo trig Cyclizations of N-CinnamylTosylamides. — Formation of azetidines via 4-endo cyclization of allylicamines is achieved. The reaction is proposed to proceed via a carbocationintermediate. — (ROBIN, SYLVIE; ROUSSEAU, GERARD; Eur. J. Org.Chem. (2000) 17, 3007-3011; Lab. Carbocycles, CNRS, Inst. Chim. Mol.Orsay, Univ. Paris-Sud, F-91405 Orsay, Fr.; EN)

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