One-pot synthesis of polycyclic isoindolines using isoindole umpolung. 2020

Rachel A Weintraub, and Wei He, and Xiang Wang
Department of Chemistry, University of Colorado, Boulder, CO 80309, USA.

Using an isoindole umpolung strategy, a one-pot synthesis of polycyclic isoindolines was accomplished. In this reaction, the in situ-generated nucleophilic isoindoles were converted to electrophilic isoindoliums via protonation, which underwent a Pictet-Spengler-type cyclization to afford a variety of polycyclic isoindolines in good yields.

UI MeSH Term Description Entries

Related Publications

Rachel A Weintraub, and Wei He, and Xiang Wang
January 2018, Organic letters,
Rachel A Weintraub, and Wei He, and Xiang Wang
December 2009, The Journal of organic chemistry,
Rachel A Weintraub, and Wei He, and Xiang Wang
September 2023, Chemistry (Weinheim an der Bergstrasse, Germany),
Rachel A Weintraub, and Wei He, and Xiang Wang
August 2012, Organic & biomolecular chemistry,
Rachel A Weintraub, and Wei He, and Xiang Wang
February 2021, Organic letters,
Rachel A Weintraub, and Wei He, and Xiang Wang
May 2016, Journal of the American Chemical Society,
Rachel A Weintraub, and Wei He, and Xiang Wang
November 2006, Journal of the American Chemical Society,
Rachel A Weintraub, and Wei He, and Xiang Wang
February 2016, Organic letters,
Rachel A Weintraub, and Wei He, and Xiang Wang
November 2021, Molecular diversity,
Rachel A Weintraub, and Wei He, and Xiang Wang
October 2006, Organic letters,
Copied contents to your clipboard!