Issue 43, 2019

A gold-triggered dearomative spirocarbocyclization/Diels–Alder reaction cascade towards diverse bridged N-heterocycles

Abstract

A rapid approach for the diversity-oriented synthesis of complex bridged polycyclic N-heterocycles from readily available starting materials in two operational steps has been developed. This strategy firstly introduces molecular diversity by an Ugi four-component reaction, and then achieves these bridged N-heterocycles via an efficient gold-triggered chemo- and diastereoselective cascade non-oxidative ortho-dearomative spirocarbocyclization/Diels–Alder reaction sequence. The application of microwave irradiation for this cascade process efficiently shortens the reaction time to 10 minutes and improves the diastereoselectivity.

Graphical abstract: A gold-triggered dearomative spirocarbocyclization/Diels–Alder reaction cascade towards diverse bridged N-heterocycles

Supplementary files

Article information

Article type
Paper
Submitted
08 Sep 2019
Accepted
23 Oct 2019
First published
23 Oct 2019

Org. Biomol. Chem., 2019,17, 9529-9536

A gold-triggered dearomative spirocarbocyclization/Diels–Alder reaction cascade towards diverse bridged N-heterocycles

Y. He, T. Narmon, D. Wu, Z. Li, L. Van Meervelt and E. V. Van der Eycken, Org. Biomol. Chem., 2019, 17, 9529 DOI: 10.1039/C9OB01967G

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