The role of hard Lewis acids in the tunning of the exo/endo stereoselectivity in Diels-Alder reactions: ab initio calculations

Journal of Molecular Structure: THEOCHEM

Volumn 358, Issue 1-3 C, 1995, Pages 23-27

  González, Javier ^a   Sordo, Tomás L ^a   Sordo, JoséA ^a  

^a UNIVERSITY OF OVIEDO   (Spain)

Author keywords

Ab initio calculations; Catalysed reactions; Diels Alder reactions; Hard Lewis acid; Stereoselectivity

Indexed keywords

EID: 58149212027     PISSN: 01661280     EISSN: None     Source Type: Journal    
DOI: 10.1016/0166-1280(95)04358-6     Document Type: Article

References (22)

1. Optimization of equilibrium geometries and transition structures
2. Solvent effects on hetero Diels?Alder reactions of sulfur dioxide with 1,3-dienes
3. Ab Initio Study of the Thermal and Lewis Acid-Catalyzed Hetero Diels-Alder Reactions of 1,3-Butadiene and Isoprene with Sulfur Dioxide
4. Theoretical analysis of the thermal and Lewis acid catalyzed reactions of butadiene and acrolein