New preparation method of highly reactive electrogenerated zinc and its use in cross-coupling reaction of functionalized organic bromides with aryl halides by using electrochemical method

A new highly reactive zinc metal was readily prepared by electrolysis of a DMF solution containing polyaromatic compounds (PA) as a mediator and a supporting electrolyte in a one-compartment cell fitted with a platinum cathode and a zinc anode. This reactive zinc (EGZn/PA) was used for transformatio...

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Main Authors: Abdul Jalil, Aishah, Sundang, Murni, Triwahyono, Sugeng, Muhd. Muhid, Muhd. Nazlan, Kurono, Nobuhito, Tokuda, Masao
Format: Conference or Workshop Item
Language:English
Published: 2005
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Online Access:http://eprints.utm.my/id/eprint/5244/1/AishahAbdulJalil2005_NewPreparationMethodOfHighlyReactive.pdf
http://eprints.utm.my/id/eprint/5244/
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spelling my.utm.52442017-08-28T07:47:55Z http://eprints.utm.my/id/eprint/5244/ New preparation method of highly reactive electrogenerated zinc and its use in cross-coupling reaction of functionalized organic bromides with aryl halides by using electrochemical method Abdul Jalil, Aishah Sundang, Murni Triwahyono, Sugeng Muhd. Muhid, Muhd. Nazlan Kurono, Nobuhito Tokuda, Masao T Technology (General) A new highly reactive zinc metal was readily prepared by electrolysis of a DMF solution containing polyaromatic compounds (PA) as a mediator and a supporting electrolyte in a one-compartment cell fitted with a platinum cathode and a zinc anode. This reactive zinc (EGZn/PA) was used for transformation of organic bromides into the corresponding organozinc bromides, which can not be achieved by the use of either reactive zinc (EGZn) or usual zinc metals. Reaction of the organozinc compounds thus prepared with various aryl iodides in the presence of 5 mol% of palladium catalyst gave the corresponding cross-coupling products in high yields. Arylzinc halides were also prepared by the use EGZn/PA, and they were reacted with other aryl halides to give the corresponding cross-coupled biaryl in good yields. 2005 Conference or Workshop Item PeerReviewed application/pdf en http://eprints.utm.my/id/eprint/5244/1/AishahAbdulJalil2005_NewPreparationMethodOfHighlyReactive.pdf Abdul Jalil, Aishah and Sundang, Murni and Triwahyono, Sugeng and Muhd. Muhid, Muhd. Nazlan and Kurono, Nobuhito and Tokuda, Masao (2005) New preparation method of highly reactive electrogenerated zinc and its use in cross-coupling reaction of functionalized organic bromides with aryl halides by using electrochemical method. In: 2nd International Conference on Chemical and Bioprocess Engineering in conjunction with 19th Symposium of Malaysian Chemical Engineers (SOMChE 2005), 8-10 December 2005, Kota Kinabalu, Sabah. (Submitted)
institution Universiti Teknologi Malaysia
building UTM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Malaysia
content_source UTM Institutional Repository
url_provider http://eprints.utm.my/
language English
topic T Technology (General)
spellingShingle T Technology (General)
Abdul Jalil, Aishah
Sundang, Murni
Triwahyono, Sugeng
Muhd. Muhid, Muhd. Nazlan
Kurono, Nobuhito
Tokuda, Masao
New preparation method of highly reactive electrogenerated zinc and its use in cross-coupling reaction of functionalized organic bromides with aryl halides by using electrochemical method
description A new highly reactive zinc metal was readily prepared by electrolysis of a DMF solution containing polyaromatic compounds (PA) as a mediator and a supporting electrolyte in a one-compartment cell fitted with a platinum cathode and a zinc anode. This reactive zinc (EGZn/PA) was used for transformation of organic bromides into the corresponding organozinc bromides, which can not be achieved by the use of either reactive zinc (EGZn) or usual zinc metals. Reaction of the organozinc compounds thus prepared with various aryl iodides in the presence of 5 mol% of palladium catalyst gave the corresponding cross-coupling products in high yields. Arylzinc halides were also prepared by the use EGZn/PA, and they were reacted with other aryl halides to give the corresponding cross-coupled biaryl in good yields.
format Conference or Workshop Item
author Abdul Jalil, Aishah
Sundang, Murni
Triwahyono, Sugeng
Muhd. Muhid, Muhd. Nazlan
Kurono, Nobuhito
Tokuda, Masao
author_facet Abdul Jalil, Aishah
Sundang, Murni
Triwahyono, Sugeng
Muhd. Muhid, Muhd. Nazlan
Kurono, Nobuhito
Tokuda, Masao
author_sort Abdul Jalil, Aishah
title New preparation method of highly reactive electrogenerated zinc and its use in cross-coupling reaction of functionalized organic bromides with aryl halides by using electrochemical method
title_short New preparation method of highly reactive electrogenerated zinc and its use in cross-coupling reaction of functionalized organic bromides with aryl halides by using electrochemical method
title_full New preparation method of highly reactive electrogenerated zinc and its use in cross-coupling reaction of functionalized organic bromides with aryl halides by using electrochemical method
title_fullStr New preparation method of highly reactive electrogenerated zinc and its use in cross-coupling reaction of functionalized organic bromides with aryl halides by using electrochemical method
title_full_unstemmed New preparation method of highly reactive electrogenerated zinc and its use in cross-coupling reaction of functionalized organic bromides with aryl halides by using electrochemical method
title_sort new preparation method of highly reactive electrogenerated zinc and its use in cross-coupling reaction of functionalized organic bromides with aryl halides by using electrochemical method
publishDate 2005
url http://eprints.utm.my/id/eprint/5244/1/AishahAbdulJalil2005_NewPreparationMethodOfHighlyReactive.pdf
http://eprints.utm.my/id/eprint/5244/
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score 13.211869