Non-hydrolytic chemoselective cleavage of Ugi tertiary amides: A mild access to N-substituted α-amino acid amides-Reference-Cited by-同舟云学术

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Non-hydrolytic chemoselective cleavage of Ugi tertiary amides: A mild access to N-substituted α-amino acid amides

Published:2018-03 Issue:13 Volume:59 Page:1196-1199
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Giustiniano Mariateresa,Pelliccia Sveva,Novellino Ettore,Tron Gian Cesare

Funder

University of Naples Federico II

University of Piemonte Orientale

AIRC

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference37 articles.

1. Highly Enantioselective Phase-Transfer-Catalyzed Alkylation of Protected α-Amino Acid Amides toward Practical Asymmetric Synthesis of Vicinal Diamines, α-Amino Ketones, and α-Amino Alcohols

2. Preparation of Hydantoins by Catalytic Oxidative Carbonylation of α-Amino Amides

3. Solid-Phase Synthesis of Amino- and Carboxyl-Functionalized Unnatural α-Amino Acid Amides

4. Lewis Acid Mediated [2,3]-Sigmatropic Rearrangement of Allylic α-Amino Amides

Cited by 1 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. Efficient Multicomponent Synthesis of Novel Rhodanine Based Amide Derivatives;Organic Preparations and Procedures International;2019-08-20

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