Formal [3+2] Annulation Involving Allylic Bromides and Thioureas. Synthesis of 2-Iminothiazolidines through a Base-Catalyzed Intramolecularanti-Michael Addition-Reference-Cited by-同舟云学术

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Formal [3+2] Annulation Involving Allylic Bromides and Thioureas. Synthesis of 2-Iminothiazolidines through a Base-Catalyzed Intramolecularanti-Michael Addition

Published:2015-02-23 Issue:4 Volume:357 Page:829-833
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Ferreira Misael,Sá Marcus M.

Publisher

Wiley

Subject

General Chemistry

Reference49 articles.

1. Multicomponent reactions: advanced tools for sustainable organic synthesis

2. Sustainable Practices in Medicinal Chemistry: Current State and Future Directions

3. The domino way to heterocycles

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1. Palladium-Catalyzed anti-Michael-Type Hydroamination of N-(Quinolin-8-yl)acrylamide with 2-Pyridones;Organic Letters;2024-07-24

2. Mild and Stereoselective Synthesis of (1E,3E)-Dienes through Silver(I)-Catalyzed β-Hydride Migration from Allylic α-Diazo Esters;Synthesis;2024-07-18

3. Palladium-Catalyzed anti-Michael-Type (Hetero)arylation of Acrylamides;Journal of the American Chemical Society;2024-05-14

4. Zinc Tetrafluoroborate-Mediated Ring Expansion of trans-Aziridine-2-carboxylates to cis-2-Iminothiazolidines and cis-Thiazolidine-2-iminium Tetrafluoroborates and Evaluation of Antimicrobial Activity;ACS Omega;2023-08-08

5. The anti-inflammatory activity of 2-iminothiazolidines: evidence for macrophage repolarization;Inflammopharmacology;2022-10-22

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