Influence of polar groups in thermal and Lewis acid promoted asymmetric diels-alder additions: lactic acid derivatives as practical highly selective and configurationally dichotomic reagents
- 31 December 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (21), 2191-2194
- https://doi.org/10.1016/s0040-4039(01)80207-0
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Asymmetrische Diels-Alder-ReaktionenNachrichten aus Chemie, Technik und Laboratorium, 1983
- Asymmetric Diels-Alder reaction: design of chiral dienophilesThe Journal of Organic Chemistry, 1983
- 2-Norbornanediazonium ions revisitedJournal of the American Chemical Society, 1983
- High asymmetric induction in diels-alder additions of cyclopentadiene to acrylates derived from isoborneolTetrahedron Letters, 1982
- Functional Groups at Concave Sites: Asymmetric Diels‐Alder Synthesis with Almost Complete (Lewis‐Acid Catalyzed) or High (Uncatalyzed) StereoselectivityAngewandte Chemie International Edition in English, 1981
- Funktionelle Gruppen in konkaver Lage: Asymmetrische Diels‐Alder‐Synthese mit nahezu vollständiger (Lewis‐Säure‐katalysiert) und hoher (unkatalysiert) StereoselektivitätAngewandte Chemie, 1981
- A convenient synthesis of methacrylatesThe Journal of Organic Chemistry, 1977
- Asymmetrische induktion bei diels-alder-reaktionenTetrahedron Letters, 1966
- The Correlation of Solvent Effects on the Stereoselectivities of Diels-Alder Reactions by Means of Linear Free Energy Relationships. A New Empirical Measure of Solvent PolarityJournal of the American Chemical Society, 1962
- The Absolute Configurations of Some Simple Norbornane Derivatives. A Test of the “Conformational Asymmetry” Model1aJournal of the American Chemical Society, 1961