Expedient and modular access to 2-azabicyclic architectures by iron-catalyzed dehydrative coupling of alcohol-bearing allylic lactams

Authors

Katie Hovenkotter, Central Washington University
Hannah Braunstein, Central Washington University
Spencer Langevin, Central Washington University
Timothy K. Beng, Central Washington UniversityFollow

Document Type

Article

Department or Administrative Unit

Chemistry

Publication Date

1-16-2017

Abstract

A high-yielding, cost-effective, modular and environmentally benign approach to [5,5]- or [6,5]-2-azabicyclic architectures bearing vicinal stereocenters, by Fe-catalyzed intramolecular dehydrative coupling of readily affordable alcohol-bearing allylic lactams is presented.

Comments

This article was originally published in Organic & Biomolecular Chemistry. The full-text article from the publisher can be found here.

Due to copyright restrictions, this article is not available for free download from ScholarWorks @ CWU.

Recommended Citation

Hovenkotter, K., Braunstein, H., Langevin, S., & Beng, T. K. (2017). Expedient and modular access to 2-azabicyclic architectures by iron-catalyzed dehydrative coupling of alcohol-bearing allylic lactams. Organic & Biomolecular Chemistry, 15(5), 1217–1221. https://doi.org/10.1039/c6ob02652d

Journal

Organic & Biomolecular Chemistry