The reaction of a particularly electrophilic acyclic diaminocarbene with carbon monoxide: formation of β- and γ-lactams
Author:
Affiliation:
1. Institut für Chemie, Universität Kassel , Heinrich-Plett-Straße 40 , 34132 Kassel , Germany
2. Institut für Chemie, Universität Kassel , Heinrich-Plett-Straße 40 , 34132 Kassel , Germany , Fax: +49 561 804 4777
Abstract
Funder
Deutsche Forschungsgemeinschaft
Publisher
Walter de Gruyter GmbH
Subject
General Chemistry
Link
https://www.degruyter.com/document/doi/10.1515/znb-2018-0255/pdf
Reference38 articles.
1. V. P. Boyarskiy, N. A. Bokach, K. V. Luzyanin, V. Yu. Kukushkin, Chem. Rev.2015, 115, 2698.
2. M. A. Kinzhalov, V. P. Boyarski, Russ. J. Gen. Chem.2015, 85, 2313.
3. L. M. Slaughter in N-Heterocyclic Carbenes (Ed.: S. P. Nolan), Wiley-VCH, Weinheim, 2014, p. 499.
4. V. P. Boyarskiy, K. V. Luzyanin, V. Yu. Kukushkin in Advances in Organometallic Chemistry and Catalysis: The Silver/Gold Jubilee International Conference on Organometallic Chemistry Celebratory Book (Ed.: A. J. L. Pombeiro), Wiley, Hoboken, NJ, 2014, p. 145.
5. H. G. Raubenheimer, Angew. Chem. Int. Ed.2012, 51, 5042.
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3. Evaluation of benzthiazolidine-based formamidinium salts for the synthesis of penem-type β-lactams by uncatalysed carbonylation of acyclic diaminocarbenes;Zeitschrift für Naturforschung B;2019-03-12
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