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2001 diastereoselective syntheses, enantioselective syntheses diastereoselective syntheses, enantioselective syntheses (incl. cis/trans-isomerism) O 0031 25 - 030 Regio- and Diastereoselective Cycloaddition of N-Methyl Nitrones Derived from 3-(Allylamino)propionaldehydes. High degree of stereocontrol can be observed in cycloaddition reactions of N-methyl nitrones [cf. (III)] derived from 3-allylaminopropionaldehydes. Best results are achieved in reactions of nitrones bearing a methyl group at the 3-position. — (TANAKA, MASAYUKI; HIKATA, JUN; YAMAMOTO, HIDETOSHI; NOGUCHI, MICHIHIKO; Heterocycles 55 (2001) 2, 223-226; Dep. Appl. Chem., Fac. Eng., Yamaguchi Univ., Tokiwadai, Ube, Yamaguchi 755, Japan; EN) 1

ChemInform Abstract: Regio- and Diastereoselective Cycloaddition of N-Methyl Nitrones Derived from 3-(Allylamino)propionaldehydes

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Page 1: ChemInform Abstract: Regio- and Diastereoselective Cycloaddition of N-Methyl Nitrones Derived from 3-(Allylamino)propionaldehydes

2001 diastereoselective syntheses, enantioselective syntheses

diastereoselective syntheses, enantioselective syntheses (incl. cis/trans-isomerism)O 0031

25 - 030Regio- and Diastereoselective Cycloaddition of N-Methyl NitronesDerived from 3-(Allylamino)propionaldehydes. — High degree ofstereocontrol can be observed in cycloaddition reactions of N-methyl nitrones [cf.(III)] derived from 3-allylaminopropionaldehydes. Best results are achieved inreactions of nitrones bearing a methyl group at the 3-position. — (TANAKA,MASAYUKI; HIKATA, JUN; YAMAMOTO, HIDETOSHI; NOGUCHI,MICHIHIKO; Heterocycles 55 (2001) 2, 223-226; Dep. Appl. Chem., Fac. Eng.,Yamaguchi Univ., Tokiwadai, Ube, Yamaguchi 755, Japan; EN)

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