Unusual Stereo- and Regioselectivity Observed in Cycloadditions of the N-Titanated Azomethine Ylides Derived from t-Butyl (Benzylideneamino)acetate with α,β-Unsaturated Esters
- 1 January 1990
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 19 (1) , 105-108
- https://doi.org/10.1246/cl.1990.105
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Generation of an N-Sodioazomethine Ylide and Its Cycloadditions with α,β-Unsaturated EstersBulletin of the Chemical Society of Japan, 1989
- Cycloaddition vs. Michael Addition in the Metal Halide/Amine-Induced Reactions of α-(Alkylideneamino) Esters with Electron-Deficient OlefinsBulletin of the Chemical Society of Japan, 1989
- Ti(IV) mediated transesterification and regio- and stereo-specific cycloaddition of imines of α-amino esters. Reversal of normal regiochemistryTetrahedron Letters, 1989
- 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
- X-Y-ZH Systems as potential 1,3-dipolesTetrahedron, 1988
- Regioselective cycloadditions of N-protonated azomethine ylides and 2-azaallyl anions generated from N-(silylmethyl) thioimidates, synthetic equivalents of nonstabilized nitrile ylidesThe Journal of Organic Chemistry, 1987