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Facile synthesis of N- (4-bromophenyl)-1- (3-bromothiophen-2-yl)methanimine derivatives via Suzuki cross-coupling reaction: their characterization and DFT studies

A variety of imine derivatives have been synthesized via Suzuki cross coupling of N-(4-bromophenyl)-1-(3-bromothiophen-2-yl)methanimine with various arylboronic acids in moderate to good yields (58–72%). A wide range of electron donating and withdrawing functional groups were well tolerated in react...

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Main Authors: Rizwan, Komal, Rasool, Nasir, Rehman, Ravya, Mahmood, Tariq, Ayub, Khurshid, Rasheed, Tahir, Ahmad, Gulraiz, Malik, Ayesha, Khan, Shakeel Ahmad, Akhtar, Muhammad Nadeem, Noorjahan Banu, Alitheen, Muhammad Nazirul, Mubin Aziz
格式: Article
語言:English
出版: Springer Open 2018
主題:
QC Physics
在線閱讀:http://umpir.ump.edu.my/id/eprint/21781/1/Facile%20synthesis%20of%20N-.pdf
http://umpir.ump.edu.my/id/eprint/21781/
https://doi.org/10.1186/s13065-018-0451-0
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spelling my.ump.umpir.217812018-07-25T03:26:33Z http://umpir.ump.edu.my/id/eprint/21781/ Facile synthesis of N- (4-bromophenyl)-1- (3-bromothiophen-2-yl)methanimine derivatives via Suzuki cross-coupling reaction: their characterization and DFT studies Rizwan, Komal Rasool, Nasir Rehman, Ravya Mahmood, Tariq Ayub, Khurshid Rasheed, Tahir Ahmad, Gulraiz Malik, Ayesha Khan, Shakeel Ahmad Akhtar, Muhammad Nadeem Noorjahan Banu, Alitheen Muhammad Nazirul, Mubin Aziz QC Physics A variety of imine derivatives have been synthesized via Suzuki cross coupling of N-(4-bromophenyl)-1-(3-bromothiophen-2-yl)methanimine with various arylboronic acids in moderate to good yields (58–72%). A wide range of electron donating and withdrawing functional groups were well tolerated in reaction conditions. To explore the structural properties, Density functional theory (DFT) investigations on all synthesized molecules (3a–3i) were performed. Conceptual DFT reactivity descriptors and molecular electrostatic potential analyses were performed by using B3LYP/6-31G(d,p) method to explore the reactivity and reacting sites of all derivatives (3a–3i). Springer Open 2018 Article PeerReviewed pdf en cc_by http://umpir.ump.edu.my/id/eprint/21781/1/Facile%20synthesis%20of%20N-.pdf Rizwan, Komal and Rasool, Nasir and Rehman, Ravya and Mahmood, Tariq and Ayub, Khurshid and Rasheed, Tahir and Ahmad, Gulraiz and Malik, Ayesha and Khan, Shakeel Ahmad and Akhtar, Muhammad Nadeem and Noorjahan Banu, Alitheen and Muhammad Nazirul, Mubin Aziz (2018) Facile synthesis of N- (4-bromophenyl)-1- (3-bromothiophen-2-yl)methanimine derivatives via Suzuki cross-coupling reaction: their characterization and DFT studies. Chemistry Central Journal, 12 (18). pp. 1-9. ISSN 1752-153X. (Published) https://doi.org/10.1186/s13065-018-0451-0 doi: 10.1186/s13065-018-0451-0
institution Universiti Malaysia Pahang Al-Sultan Abdullah
building UMPSA Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Pahang Al-Sultan Abdullah
content_source UMPSA Institutional Repository
url_provider http://umpir.ump.edu.my/
language English
topic QC Physics
spellingShingle QC Physics
Rizwan, Komal
Rasool, Nasir
Rehman, Ravya
Mahmood, Tariq
Ayub, Khurshid
Rasheed, Tahir
Ahmad, Gulraiz
Malik, Ayesha
Khan, Shakeel Ahmad
Akhtar, Muhammad Nadeem
Noorjahan Banu, Alitheen
Muhammad Nazirul, Mubin Aziz
Facile synthesis of N- (4-bromophenyl)-1- (3-bromothiophen-2-yl)methanimine derivatives via Suzuki cross-coupling reaction: their characterization and DFT studies
description A variety of imine derivatives have been synthesized via Suzuki cross coupling of N-(4-bromophenyl)-1-(3-bromothiophen-2-yl)methanimine with various arylboronic acids in moderate to good yields (58–72%). A wide range of electron donating and withdrawing functional groups were well tolerated in reaction conditions. To explore the structural properties, Density functional theory (DFT) investigations on all synthesized molecules (3a–3i) were performed. Conceptual DFT reactivity descriptors and molecular electrostatic potential analyses were performed by using B3LYP/6-31G(d,p) method to explore the reactivity and reacting sites of all derivatives (3a–3i).
format Article
author Rizwan, Komal
Rasool, Nasir
Rehman, Ravya
Mahmood, Tariq
Ayub, Khurshid
Rasheed, Tahir
Ahmad, Gulraiz
Malik, Ayesha
Khan, Shakeel Ahmad
Akhtar, Muhammad Nadeem
Noorjahan Banu, Alitheen
Muhammad Nazirul, Mubin Aziz
author_facet Rizwan, Komal
Rasool, Nasir
Rehman, Ravya
Mahmood, Tariq
Ayub, Khurshid
Rasheed, Tahir
Ahmad, Gulraiz
Malik, Ayesha
Khan, Shakeel Ahmad
Akhtar, Muhammad Nadeem
Noorjahan Banu, Alitheen
Muhammad Nazirul, Mubin Aziz
author_sort Rizwan, Komal
title Facile synthesis of N- (4-bromophenyl)-1- (3-bromothiophen-2-yl)methanimine derivatives via Suzuki cross-coupling reaction: their characterization and DFT studies
title_short Facile synthesis of N- (4-bromophenyl)-1- (3-bromothiophen-2-yl)methanimine derivatives via Suzuki cross-coupling reaction: their characterization and DFT studies
title_full Facile synthesis of N- (4-bromophenyl)-1- (3-bromothiophen-2-yl)methanimine derivatives via Suzuki cross-coupling reaction: their characterization and DFT studies
title_fullStr Facile synthesis of N- (4-bromophenyl)-1- (3-bromothiophen-2-yl)methanimine derivatives via Suzuki cross-coupling reaction: their characterization and DFT studies
title_full_unstemmed Facile synthesis of N- (4-bromophenyl)-1- (3-bromothiophen-2-yl)methanimine derivatives via Suzuki cross-coupling reaction: their characterization and DFT studies
title_sort facile synthesis of n- (4-bromophenyl)-1- (3-bromothiophen-2-yl)methanimine derivatives via suzuki cross-coupling reaction: their characterization and dft studies
publisher Springer Open
publishDate 2018
url http://umpir.ump.edu.my/id/eprint/21781/1/Facile%20synthesis%20of%20N-.pdf
http://umpir.ump.edu.my/id/eprint/21781/
https://doi.org/10.1186/s13065-018-0451-0
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score 13.250246

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