Synthesis of Bis(functionalized) Aminals via Successive Nucleophilic Amidation and Amination-Reference-Cited by-同舟云学术

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Synthesis of Bis(functionalized) Aminals via Successive Nucleophilic Amidation and Amination

Published:2023-02-06 Issue:4 Volume:88 Page:2207-2213
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Iwai Kento¹²^ORCID,Hikasa Akari¹,Yoshioka Kotaro³,Tani Shinki³,Umezu Kazuto³,Nishiwaki Nagatoshi¹²^ORCID

Affiliation:

1. School of Engineering Science, Kochi University of Technology, Tosayamada, Kami 782-8502, Kochi, Japan

2. Research Center for Molecular Design, Kochi University of Technology, Tosayamada, Kami 782-8502, Kochi, Japan

3. Kumiai Chemical Industry Co. Ltd., Nakanogo, Fuji 421-3306, Shizuoka, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c02647

Reference28 articles.

1. aBanning, J. H.; Wu, B.; Starr, N. G.; Drappel, S. V. Phase change ink comprising a carrier made of a branched triamide and azo dye colorant. DE102014216775, 2015.

2. Unusual Expansion of the 1,2,4,5-Tetrazine Ring in [1,2,4]Triazolo[4,3-b][1,2,4,5]tetrazines Leading to [1,2,4,6]Tetrazepine Systems

3. cGoldfarb, D. S. Method using lifespan-altering compounds for altering the lifespan of eukaryotic organisms, and screening for such compounds. US0163545, 2009.

4. A model study for a novel synthetic approach to 2-carboxyinosines

5. Inhibition of the HIF1α-p300 interaction by quinone- and indandione-mediated ejection of structural Zn(II)

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