Stereoselective Nucleophilc Substitution of α-Bromo Tertiary Amides for Asymmetric Synthesis of Highly Substituted 2,5-Diketopiperazines
Author:
Affiliation:
1. Department of Chemistry; Konkuk University; Seoul 05029 Korea
Funder
Konkuk University
Publisher
Wiley
Subject
General Chemistry
Reference19 articles.
1. 2,5-Diketopiperazines: Synthesis, Reactions, Medicinal Chemistry, and Bioactive Natural Products
2. The design of orally bioavailable 2, 5-diketopiperazine oxytocin antagonists: from concept to clinical candidate for premature labor
3. CyclicisoDGR and RGD Peptidomimetics Containing Bifunctional Diketopiperazine Scaffolds are Integrin Antagonists
4. Synthesis and Biological Evaluations of a Series of Thaxtomin Analogues
5. Synthesis and Evaluation of Tryprostatin B and Demethoxyfumitremorgin C Analogues
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. An intramolecular hydrogen bond-promoted “green” Ugi cascade reaction for the synthesis of 2,5-diketopiperazines with anticancer activity;RSC Advances;2022
2. The Fascinating Chemistry of α‐Haloamides;ChemistryOpen;2020-01-13
3. ChemInform Abstract: Stereoselective Nucleophilc Substitution of α-Bromo Tertiary Amides for Asymmetric Synthesis of Highly Substituted 2,5-Diketopiperazines.;ChemInform;2016-09
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