Volume 38, Issue 4 pp. 389-393
Concise Report

Iron-Catalyzed Aminomethyloxygenative Cyclization of Hydroxy-α-diazoesters with N,O-Aminals

Suchen Zou

Suchen Zou

Hefei National Laboratory for Physical Sciences at the Microscale and Department of Chemistry, Center for Excellence in Molecular Synthesis, University of Science and Technology of China, Chinese Academy of Sciences, Hefei, Anhui, 230026 China

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Tianze Zhang

Tianze Zhang

Hefei National Laboratory for Physical Sciences at the Microscale and Department of Chemistry, Center for Excellence in Molecular Synthesis, University of Science and Technology of China, Chinese Academy of Sciences, Hefei, Anhui, 230026 China

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Siyuan Wang

Siyuan Wang

Hefei National Laboratory for Physical Sciences at the Microscale and Department of Chemistry, Center for Excellence in Molecular Synthesis, University of Science and Technology of China, Chinese Academy of Sciences, Hefei, Anhui, 230026 China

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Hanmin Huang

Corresponding Author

Hanmin Huang

Hefei National Laboratory for Physical Sciences at the Microscale and Department of Chemistry, Center for Excellence in Molecular Synthesis, University of Science and Technology of China, Chinese Academy of Sciences, Hefei, Anhui, 230026 China

State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou, Gansu, 730000 China

E-mail: [email protected]Search for more papers by this author
First published: 17 January 2020
Citations: 11

Summary of main observation and conclusion

A new and efficient cyclization reaction has been developed to synthesize cyclic α,α-disubstituted β-amino esters via iron-catalyzed intramolecular aminomethyloxygenative cyclization of diazo compounds with N,O-aminal under mild reaction conditions. A broad range of hydroxy-α-diazoesters with different substituents and various N,O-aminals were compatible with this protocol, affording the corresponding α,α-disubstituted β-amino esters bearing a five- to eight-membered oxacycle in good yields.

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