Not‐So‐Innocent Anions Determine the Mechanism of Cationic Alkylators-Reference-Cited by-同舟云学术

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Not‐So‐Innocent Anions Determine the Mechanism of Cationic Alkylators

Published:2021-01-18 Issue:10 Volume:27 Page:3440-3448
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chemistry A European J

Author:

Taimoory S. Maryamdokht¹²^ORCID,Cataldo Vincenzo Alessandro³^ORCID,Schäfer Andreas⁴,Trant John F.¹,Guterman Ryan³^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry University of Windsor 401 Sunset Ave. ON N9B 3P4 Windsor Canada

2. Department of Chemistry University of Michigan 930 N University Ave. Ann Arbor MI 48109 USA

3. Colloid Chemistry Department Max Planck Institute for Colloids and Interfaces Am Mühlenberg 1 OT Golm 14476 Potsdam Germany

4. Institut für Chemie und Biochemie–Organische Chemie Freie Universität Berlin Takustr. 3 14195 Berlin Germany

Funder

Natural Sciences and Engineering Research Council of Canada

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202004208

Reference51 articles.

1. The influence of acceptor nucleophilicity on the glycosylation reaction mechanism

2. Groebke multicomponent reaction and subsequent nucleophilic aromatic substitution for a convenient synthesis of 3,8-diaminoimidazo[1,2-a]pyrazines as potential kinase inhibitors

3. Oxidative nucleophilic substitution selectively produces cambinol derivatives with antiproliferative activity on bladder cancer cell lines

4. Nucleophilic Aromatic Substitution of Methacrylamide Anion and Its Application to the Synthesis of the Anticancer Drug Bicalutamide

5. An overview of the synthetic routes to the best selling drugs containing 6-membered heterocycles

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1. Telluride-Based Pillar[5]arene: A Recyclable Catalyst for Alkylation Reactions in Aqueous Solution;The Journal of Organic Chemistry;2024-09-04

2. Divalent Benzimidazolium-Based Axles for Self-Reporting Pseudorotaxanes;The Journal of Organic Chemistry;2022-11-15

3. A Solid Alkylation: Highly Recyclable, Flow Chemistry‐Ready, Resin‐Supported Thioimidazoliums Alkylate Sulfur‐Centered Nucleophiles;European Journal of Organic Chemistry;2022-09-15

4. Easy S-Alkylation of Arylthioureas and 2-Mercaptobenzothiazoles Using Tetraalkylammonium Salts under Transition-Metal-Free Conditions;The Journal of Organic Chemistry;2022-07-27

5. From Stoichiometric Reagents to Catalytic Partners: Selenonium Salts as Alkylating Agents for Nucleophilic Displacement Reactions in Water;Advanced Synthesis & Catalysis;2021-10-27

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