π-Facial selectivity in the Diels-Alder reaction of glucosamine-based chiral furans and maleimides

Furans derived from carbohydrate feedstocks are a versatile class of bio-renewable building blocks and have been used extensively to access 7-oxanorbornenes via Diels-Alder reactions. Due to their substitution patterns these furans typically have two different π-faces and therefore furnish racemates...

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Veröffentlicht in:	Organic & biomolecular chemistry 2023-03, Vol.21 (9), p.1888-1894
Hauptverfasser:	van der Loo, Cornelis H. M, Schim van der Loeff, Rutger, Martín, Avelino, Gomez-Sal, Pilar, Borst, Mark L. G, Pouwer, Kees, Minnaard, Adriaan J
Format:	Artikel
Sprache:	eng
Schlagworte:	Carbohydrates Crystallography Diels-Alder reactions Furans Glucosamine Pesticides Selectivity Substitution reactions X-ray crystallography
Online-Zugang:	Volltext
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