Enamin/Enolat-vermittelte organokatalytische Azid-Carbonyl-[3+2]-Cycloadditionen zur Synthese von dicht funktionalisierten 1,2,3-Triazolen-Reference-Cited by-同舟云学术

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Enamin/Enolat-vermittelte organokatalytische Azid-Carbonyl-[3+2]-Cycloadditionen zur Synthese von dicht funktionalisierten 1,2,3-Triazolen

Published:2014-11-17 Issue:52 Volume:126 Page:14536-14538
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Ramasastry Sripada S. V.

Publisher

Wiley

Subject

General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ange.201409410/fullpdf

Reference50 articles.

1. 1,2,3-Triazole-[2,5-Bis-O-(tert-butyldimethylsilyl)-.beta.-D-ribofuranosyl]-3'-spiro-5''-(4''-amino-1'',2''-oxathiole 2'',2''-dioxide) (TSAO) Analogs: Synthesis and Anti-HIV-1 Activity

2. Heterocyclic HIV-1 Protease Inhibitors

3. New Lead Structures in Antifungal Drug Discovery

4. Click Chemistry: 1,2,3-Triazoles as Pharmacophores

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1. Azide–Enolate Cycloaddition‐Rearrangement Enables Direct α‐Amination of Amides and Enelactam Synthesis from Esters**;Chemistry – A European Journal;2023-03-28

2. Cycloaddition Reactions of Enamines;European Journal of Organic Chemistry;2023-02-23

3. Three‐Component Coupling of α‐Trifluoromethyl Carbonyls, Azides and Amines for the Regioselective Synthesis of 1,4,5‐Trisubstituted 1,2,3‐Triazoles;Advanced Synthesis & Catalysis;2022-03-22

4. Alkyne Surrogates in Cycloaddition Reactions for the Preparation of Molecules of Interest;Asian Journal of Organic Chemistry;2021-08-06

5. Cu(II)‐Catalysed Azide‐Alkyne Cycloaddition Reaction towards Synthesis of β‐Carboline C1‐Tethered 1,2,3‐Triazole Derivatives;ChemistrySelect;2021-04-27

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