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Rhodium-Catalyzed Tandem Asymmetric Allylic Decarboxylative Addition and Cyclization of Vinylethylene Carbonates with N-Nosylimines.


ABSTRACT: A enantioselective tandem transformation, concerning asymmetric allylic decarboxylative addition and cyclization of N-nosylimines with vinylethylene carbonates (VECs), in the presence of [Rh(C2H4)2Cl]2, chiral sulfoxide-N-olefin tridentate ligand has been developed. The reaction of VECs with various substituted N-nosylimines proceeded smoothly under mild conditions, providing highly functionalized oxazolidine frameworks in good to high yields with good to excellent enantioselectivity.

SUBMITTER: Wang XL 

PROVIDER: S-EPMC10934018 | biostudies-literature | 2024 Feb

REPOSITORIES: biostudies-literature

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Rhodium-Catalyzed Tandem Asymmetric Allylic Decarboxylative Addition and Cyclization of Vinylethylene Carbonates with <i>N</i>-Nosylimines.

Wang Xiao-Lin XL   Jiang Hai-Bin HB   Zheng Sheng-Cai SC   Zhao Xiao-Ming XM  

Molecules (Basel, Switzerland) 20240226 5


A enantioselective tandem transformation, concerning asymmetric allylic decarboxylative addition and cyclization of <i>N</i>-nosylimines with vinylethylene carbonates (VECs), in the presence of [Rh(C<sub>2</sub>H<sub>4</sub>)<sub>2</sub>Cl]<sub>2</sub>, chiral sulfoxide-<i>N</i>-olefin tridentate ligand has been developed. The reaction of VECs with various substituted <i>N</i>-nosylimines proceeded smoothly under mild conditions, providing highly functionalized oxazolidine frameworks in good to  ...[more]

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