Cycloaddition vs. Michael Addition in the Metal Halide/Amine-Induced Reactions of α-(Alkylideneamino) Esters with Electron-Deficient Olefins
- 1 March 1989
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 62 (3), 869-874
- https://doi.org/10.1246/bcsj.62.869
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Lithium bromide-triethylamine induced cycloaddition of N-alkylidene 2-amino esters and amides to electron-deficient olefins with high regio- and stereoselectivityThe Journal of Organic Chemistry, 1988
- Michael Addition and Alkylation of 2-Azaallyl Anions Derived from N-(1-Cyanoalkyl)imines, and Stereoselective Cyclization of Imine Esters or Ketones Leading to 1-PyrrolinesBulletin of the Chemical Society of Japan, 1987
- Reactivity of Cycloimmonium YlidesHETEROCYCLES, 1984
- .alpha.-Alkylation and Michael addition of amino acids - a practical methodThe Journal of Organic Chemistry, 1977
- Alkylation and Michael additions of glycine ethyl ester. Use in .alpha.-amino acid synthesis and as acyl carbanion equivalentThe Journal of Organic Chemistry, 1976
- Frontier molecular orbital theory of cycloaddition reactionsAccounts of Chemical Research, 1975
- Origin of reactivity, regioselectivity, and periselectivity in 1,3-dipolar cycloadditionsJournal of the American Chemical Society, 1973
- Frontier molecular orbitals of 1,3 dipoles and dipolarophilesJournal of the American Chemical Society, 1973