Electrophilic amination reactions with 1 H ‐indazole ‐3‐carboxylates: Synthesis of amino acid frameworks and 3‐amino ‐2‐oxindoles-Reference-Cited by-同舟云学术

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Electrophilic amination reactions with 1 H ‐indazole ‐3‐carboxylates: Synthesis of amino acid frameworks and 3‐amino ‐2‐oxindoles

Published:2020-05-14 Issue:7 Volume:57 Page:3002-3010
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:J Heterocyclic Chem

Author:

Mizota Isao¹,Mori Mayuko¹,Shimizu Makoto¹²^ORCID

Affiliation:

1. Department of Chemistry for Materials, Graduate School of EngineeringMie University Tsu Japan

2. School of Energy Science and EngineeringNanjing Tech University Nanjing China

Funder

Japan Society for the Promotion of Science

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Wiley

Subject

Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jhet.4015

Reference57 articles.

1. Design and synthesis of novel HIV-1 protease inhibitors incorporating oxyindoles as the -ligands

2. Spiroindolones, a Potent Compound Class for the Treatment of Malaria

3. AG-041R, a Gastrin/CCK-B Antagonist, Stimulates Chondrocyte Proliferation and Metabolism in Vitro

4. Stereoselective Total Synthesis of KAE609 via Direct Catalytic Asymmetric Alkynylation to Ketimine

5. Biological characterization of rodent and human vasopressin V1b receptors using SSR-149415, a nonpeptide V1b receptor ligand

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1. N-Alkylation/aldol reaction of α-aldimino thioesters: a facile three-component coupling reaction;RSC Advances;2021

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