2-Aminooxazoles as novel dienophiles in the inverse demand Diels–Alder reaction with 1,2,4-triazines-Reference-Cited by-同舟云学术

2-Aminooxazoles as novel dienophiles in the inverse demand Diels–Alder reaction with 1,2,4-triazines

Published:2021-07 Issue:4 Volume:31 Page:542-544
ISSN:0959-9436
Container-title:Mendeleev Communications
language:en
Short-container-title:Mendeleev Communications

Author:

Krinochkin Alexey P.,Mallikarjuna Reddy Guda,Kopchuk Dmitry S.,Slepukhin Pavel A.,Shtaitz Yaroslav K.,Khalymbadzha Igor A.,Kovalev Igor S.,Kim Grigory A.,Ganebnykh Ilya N.,Zyryanov Grigory V.,Chupakhin Oleg N.,Charushin Valery N.

Publisher

Elsevier BV

Subject

General Chemistry

Reference45 articles.

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3. Consecutive nucleophilic substitution and aza Diels–Alder reaction—an efficient strategy to functionalized 2,2′-bipyridines

4. Direct C H/C Li coupling of 1,2,4-triazines with C6F5Li followed by aza-Diels-Alder reaction as a pot, atom, and step economy (PASE) approach towards novel fluorinated 2,2′-bipyridine fluorophores

5. I. S. Kovalev, M. I. Savchuk, D. S. Kopchuk, G. V. Zyryanov, T. A. Pospelova, V. L. Rusinov and O. N. Chupakhin, Russ. J. Org. Chem., 2019, 55, 886 (Zh. Org. Khim., 2019, 55, 962).

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