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RhI‐Catalyzed Regio‐ and Stereospecific Carbonylation of 1‐(1‐Alkynyl)cyclopropyl Ketones: A Modular Entry to Highly Substituted 5,6‐Dihydrocyclopenta[c]furan‐4‐ones
Ist Teil von
Chemistry : a European journal, 2009-05, Vol.15 (21), p.5208-5211
Ort / Verlag
Weinheim: WILEY‐VCH Verlag
Erscheinungsjahr
2009
Link zum Volltext
Quelle
Wiley Online Library Journals Frontfile Complete
Beschreibungen/Notizen
Efficient route: A novel RhI‐catalyzed regio‐ and stereospecific carbonylation reaction of (1‐alkynyl)cyclopropyl ketones by selective activation of a carboncarbon σ bond of the cyclopropane ring was demonstrated (see scheme). This method provides a general, efficient, stereoselective route to synthesise 1,3,5‐trisubstituted and 1,3,5,6‐tetrasubstituted 5,6‐dihydrocyclopenta[c]furan‐4‐one with convertible functional groups.
Efficient route: A novel RhI‐catalyzed regio‐ and stereospecific carbonylation reaction of (1‐alkynyl)cyclopropyl ketones by selective activation of a carboncarbon σ bond of the cyclopropane ring was demonstrated (see scheme). This method provides a general, efficient, stereoselective route to synthesise 1,3,5‐trisubstituted and 1,3,5,6‐tetrasubstituted 5,6‐dihydrocyclopenta[c]furan‐4‐one with convertible functional groups.