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Volumn 1, Issue 20, 2003, Pages 3592-3599

Stereochemistry of intramolecular Diels-Alder furan (IMDAF) reactions of furyl-substituted chiral ethanolamides

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDES; CATALYSIS; FURAN RESINS; HYDROGEN INORGANIC COMPOUNDS; SODIUM COMPOUNDS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

EID: 0142227200     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b307275d     Document Type: Article
Times cited : (21)

References (46)
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    • note
    • Designation as the (S)-cyanohydrin results from the fact that, according to the Cahn-Ingold-Prelog rules, the 2-furyl substituent takes priority over the nitrile group.
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    • For examples see: references 21 and 22. P. A. Jacobi and Y. Li, J. Am. Chem. Soc., 2001, 123, 9307; L. Sader-Bakaouni, O. Charton, N. Kunesch and F. Tillequin, Tetrahedron, 1998, 54, 1773; F. Pontén and G. Magnusson, J. Org. Chem., 1997, 62, 7978; J. Ancerewicz and P. Vogel, Helv. Chim. Acta, 1996, 79, 1393.
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    • For examples see: references 21 and 22. P. A. Jacobi and Y. Li, J. Am. Chem. Soc., 2001, 123, 9307; L. Sader-Bakaouni, O. Charton, N. Kunesch and F. Tillequin, Tetrahedron, 1998, 54, 1773; F. Pontén and G. Magnusson, J. Org. Chem., 1997, 62, 7978; J. Ancerewicz and P. Vogel, Helv. Chim. Acta, 1996, 79, 1393.
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