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The asymmetric cyclopropanation of furan with alkyl diazaoacetates using chiral rhodium catalysts has been reported to proceed in up to 31% yield (exo/endo=71:29; exo: 14% ee, endo: 76% ee). See Ref. 7b.
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in press
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The absolute configuration of enantiomerically pure 6a-Et was determined by X-ray structure analysis (Enraf-Nonius CAD-4 diffractometer, ω/2θ scans, Cu Kα radiation) and further confirmed by conversion of 6a to paraconic acids. The absolute configuration of enantiomerically pure (ent)-8 was determined after its conversion to 11 by X-ray structural analysis. (a) Chhor, R. B.; Nosse, B.; Soergel, S.; Böhm, C.; Seitz, M.; Reiser, O. Chem. Eur. J. 2003, 9, in press; (b) Beumer, R.; Bubert, C.; Cabrele, C.; Vielhauer, O.; Pietzsch, M.; Reiser, O. J. Org. Chem. 2000, 65, 8960-8969.
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0034731625
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The absolute configuration of enantiomerically pure 6a-Et was determined by X-ray structure analysis (Enraf-Nonius CAD-4 diffractometer, ω/2θ scans, Cu Kα radiation) and further confirmed by conversion of 6a to paraconic acids. The absolute configuration of enantiomerically pure (ent)-8 was determined after its conversion to 11 by X-ray structural analysis. (a) Chhor, R. B.; Nosse, B.; Soergel, S.; Böhm, C.; Seitz, M.; Reiser, O. Chem. Eur. J. 2003, 9, in press; (b) Beumer, R.; Bubert, C.; Cabrele, C.; Vielhauer, O.; Pietzsch, M.; Reiser, O. J. Org. Chem. 2000, 65, 8960-8969.
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