Tuning of Copper-Catalyzed Multicomponent Reactions toward 3-Functionalized Oxindoles
01 natural sciences
0104 chemical sciences
DOI:
10.1021/acs.orglett.6b00964
Publication Date:
2016-05-05T13:37:56Z
AUTHORS (4)
ABSTRACT
A tunable copper-catalyzed azide–alkyne cycloaddition (CuAAC)-initiated multicomponent reaction strategy for the construction of 3-functionalized indolin-2-ones is reported. Upon controlling ring opening four-membered O-heterocyclic intermediates, this unique method enables divergent derivatization N-protected isatins to give three-component (3-CR) and four-component (4-CR) adducts, respectively.
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