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Improved enantioselection for chiral dirhodium(II) carboxamide-catalysed carbon-hydrogen insertion reactions of tertiary alkyl diazoacetates

✍ Scribed by Michael P. Doyle; Qi-Lin Zhou; Conrad E. Raab; Gregory H.P. Roos


Book ID
103400289
Publisher
Elsevier Science
Year
1995
Tongue
French
Weight
201 KB
Volume
36
Category
Article
ISSN
0040-4039

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N-Benzyl-2-deoxyxylonolactams are accessible by highly chemoselective, diastereoselective, and enantioselective carbon-hydrogen insertion reactions of diazoacetamides. Competing aromatic cycloaddition or b-lactam formation via carbon-hydrogen insertion into a benzylic position can be minimized by th