Rhodium(III)‐Catalyzed Redox‐Neutral Coupling of N‐Phenoxyacetamides and Alkynes with Tunable Selectivity
01 natural sciences
0104 chemical sciences
DOI:
10.1002/ange.201300881
Publication Date:
2013-04-24T12:31:10Z
AUTHORS (4)
ABSTRACT
Give it a tweak: A novel oxidizing directing group was developed for a rhodium(III)-catalyzed CH functionalization of N-phenoxyacetamides with alkynes. A small change in the reaction conditions leads to either ortho-hydroxyphenyl-substituted enamides or cyclization to deliver benzofurans with high selectivity (see scheme; Cp*=C5 Me5 ).
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