Nitroalkenes as electrophiles in the asymmetric Michael reaction involving chiral imines/enamino esters
- 21 May 1999
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 10 (10) , 2015-2021
- https://doi.org/10.1016/s0957-4166(99)00180-9
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- The origin of the stereoselectivity in the asymmetric Michael reaction using chiral imines/secondary enamines under neutral conditions: a computational investigationTetrahedron: Asymmetry, 1998
- Enantioselective Access to Five- and Six-membered Nitrogen-containing Heterocycles, Based on the Asymmetric Michael Addition of Chiral Imines and Chiral Enamino EstersHETEROCYCLES, 1998
- Stereochemical Aspects in the Asymmetric Michael Addition of Chiral Imines to Substituted Electrophilic AlkenesThe Journal of Organic Chemistry, 1996
- Asymmetric approach to Pauson-Khand bicyclization. Enantioselective formal synthesis of hirsuteneJournal of the American Chemical Society, 1990
- Conjugated nitroalkenes: versatile intermediates in organic synthesisChemical Reviews, 1986
- Conversion of γ-nitroketones to γ-diketones by the Nef reactionTetrahedron Letters, 1972
- Mild procedure for transforming nitro groups into carbonyls. Application to the synthesis of cis-jasmoneJournal of the American Chemical Society, 1971
- 280. Aliphatic nitro-compounds. Part I. Preparation of nitro-olefins by dehydration of 2-nitro-alcoholsJournal of the Chemical Society, 1947