Acid-catalyzed aza-Diels-Alder versus 1,3-dipolar cycloadditions of methyl glyoxylate oxime with cyclopentadiene

Tetrahedron Letters

Volumn 49, Issue 40, 2008, Pages 5777-5781

  Sousa, Carlos A D ^a   Vale, M Luísa C ^a   Rodríguez Borges, José E ^a   Garcia Mera, Xerardo ^b   Rodríguez Otero, Jesús ^b  

^a UNIVERSITY OF PORTO   (Portugal)

^b UNIVERSITY OF SANTIAGO DE COMPOSTELA   (Spain)

Author keywords

1,3 Dipolar cycloaddition; 2 Hydroxy 2 azabicyclo 2.2.1 heptenes; Aza Diels Alder reaction; Glyoxylate oxime; Isoxazolidines

Indexed keywords

BRONSTED ACID; DICHLOROMETHANE; GLYOXYLIC ACID DERIVATIVE; LEWIS ACID; METHYL (2 OXA 3 AZABICYCLO[3.3.0]OCT 7 ENE) 4 CARBOXYLIC ACID; METHYL [(3 ENDO) 2 HYDROXY 2 AZABICYCLO[2.2.1]HEPT 5 ENE] 3 CARBOXYLIC ACID; METHYL [(3 EXO) 2 HYDROXY 2 AZABICYCLO[2.2.1]HEPT 5 ENE] 3 CARBOXYLIC ACID; OXIME DERIVATIVE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CYCLOADDITION; DIELS ALDER REACTION; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; TEMPERATURE SENSITIVITY; X RAY CRYSTALLOGRAPHY;

ALNUS;

EID: 49549104179     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.07.110     Document Type: Article

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