Exo- and enantioselective Diels-Alder reactions: Pyrazolidinone auxiliaries as a means to enhanced exo selectivity

Synlett

Volumn , Issue 17, 2008, Pages 2655-2658

  Sibi, Mukund P ^a   Nie, Xiaoping ^a   Shackleford, Jessica P ^a   Stanley, Levi M ^a   Bouret, Frances ^a  

^a NORTH DAKOTA STATE UNIVERSITY   (United States)

Author keywords

Chiral Lewis acid; Diels Alder; Enantioselective; Exo selective; Pyrazolidinone

Indexed keywords

CYCLOPENTADIENE DERIVATIVE; LEWIS ACID; PYRAZOLIDINONE; PYRAZOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLOADDITION; DIELS ALDER REACTION; ENANTIOSELECTIVITY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SYNTHESIS;

EID: 55449123606     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0028-1083438     Document Type: Article

References (33)

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33. The identity of the exo and endo adducts was established by NMR spectroscopy. Additionally, the products were converted into known benzyl esters.