Efficient Synthesis of 4‐Bromo‐ <i>N</i> ‐(1‐phenylethyl)benzamide, Arylation by Pd(0) Catalyst, Characterization and DFT Study-Reference-Cited by-同舟云学术

Efficient Synthesis of 4‐Bromo‐ N ‐(1‐phenylethyl)benzamide, Arylation by Pd(0) Catalyst, Characterization and DFT Study

Published:2022-08 Issue:29 Volume:7 Page:
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Raza Shah Alı¹,Rasool Nasır¹,Bılal Muhammad¹,Mubarık Adeel¹,Alı Hashmı Muhammad²,Nadeem Akhtar Muhammad³,Imran Muhammad⁴⁵^ORCID,Ahmad Gulraız¹,Siddiqa Ayesha¹,Adnan Alı Shah Syed⁶⁷

Affiliation:

1. Department of Chemistry Government College University Faisalabad 38000 Pakistan

2. Department of Chemistry University of Education, Attock Campus Attock 43600 Pakistan

3. Department of Chemistry & Ghazi University Dera Ghazi Khan 32200 Pakistan

4. Department of Chemistry, Faculty of Science King Khalid University P.O. Box 9004 Abha 61413 Saudi Arabia

5. Research center for Advanced Materials Science (RCAMS) king Khalid University Abha 61514, P. O. Box 9004 Saudi Arabia

6. Faculty of Pharmacy Universiti Teknologi MARA Cawangan Selangor Kampus Puncak Alam Bandar Puncak Alam 42300 Malaysia

7. Atta-ur-Rahman Institute for Natural Products Discovery (AuRIns) Universiti Teknologi MARA Cawangan Selangor Kampus Puncak Alam Bandar Puncak Alam 42300 Malaysia

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.202200861

Reference53 articles.

1. A green chemistry perspective on catalytic amide bond formation

2. Design, synthesis, and biological evaluation of 2-amino-N-(2-methoxyphenyl)-6-((4-nitrophenyl)sulfonyl)benzamide derivatives as potent HIV-1 Vif inhibitors

3. Synthesis and structure–activity relationship of disubstituted benzamides as a novel class of antimalarial agents

4. δ-Opioid Mechanisms for ADL5747 and ADL5859 Effects in Mice: Analgesia, Locomotion, and Receptor Internalization

5. Design, synthesis and structure–activity relationships of substituted oxazole–benzamide antibacterial inhibitors of FtsZ

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