High Stereoselectivity in Lewis‐Acid‐Catalyzed and Uncatalyzed Diels–Alder Reactions of the Fumarate of (S)‐Ethyl Lactate
- 1 November 1987
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 26 (11) , 1143-1145
- https://doi.org/10.1002/anie.198711431
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Diastereoselective Diels–Alder Reaction on Carbohydrate MatricesAngewandte Chemie International Edition in English, 1987
- Diastereoselektive Diels-Alder-Reaktion an Kohlenhydrat-MatricesAngewandte Chemie, 1987
- Asymmetric diels-alder reaction. Cooperative blocking effect in organic synthesisTetrahedron Letters, 1986
- Zum Mechanismus der asymmetrischen Diels‐Alder‐Reaktion: Erste Kristallstrukturanalyse eines Lewis‐Säure‐Komplexes eines chiralen DienophilsAngewandte Chemie, 1985
- Concerning the Mechanism of the Asymmetric Diels‐Alder Reaction: First Crystal Structure Analysis of a Lewis Acid Complex of a Chiral DienophileAngewandte Chemie International Edition in English, 1985
- Influence of polar groups in thermal and Lewis acid promoted asymmetric diels-alder additions: lactic acid derivatives as practical highly selective and configurationally dichotomic reagentsTetrahedron Letters, 1984
- Transition states in catalyzed and uncatalyzed Diels-Alder reactions. Cooperativity as a probe of geometryJournal of the American Chemical Society, 1984