Highly Chemoselective Synthesis of Indolizidine Lactams by SmI2 -Induced Umpolung of the Amide Bond via Aminoketyl Radicals: Efficient Entry to Alkaloid Scaffolds-Reference-Cited by-同舟云学术

Highly Chemoselective Synthesis of Indolizidine Lactams by SmI2 -Induced Umpolung of the Amide Bond via Aminoketyl Radicals: Efficient Entry to Alkaloid Scaffolds

Published:2016-07-15 Issue:34 Volume:22 Page:11949-11953
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Shi Shicheng¹,Lalancette Roger¹,Szostak Roman²,Szostak Michal¹^ORCID

Affiliation:

1. Department of Chemistry; Rutgers University; 73 Warren Street Newark NJ 07102 USA

2. Department of Chemistry; Wroclaw University; 14 F. Joliot-Curie Street Wroclaw 50-383 Poland

Funder

Rutgers University

NSF-MRI

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201602717/fullpdf

Reference124 articles.

1. Reagent-Controlled Transition-Metal-Catalyzed Radical Reactions

2. Beyond Samarium Diiodide: Vistas in Reductive Chemistry Mediated by Lanthanides(II)

3. Jenseits von Samariumdiiodid: Perspektiven für Lanthanoid(II)-vermittelte Reduktionen

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