Solvent-free reduction of carboxylic acids to alcohols with NaBH<inf>4</inf> promoted by 2,4,6-trichloro-1,3,5-triazine and PPh<inf>3</inf> in the presence of K<inf>2</inf>CO<inf>3</inf>
© the Partner Organisations 2014. A simple, rapid, and eco-friendly method for NaBH4 reduction of carboxylic acids to alcohols under solvent-free conditions was developed using a combination of 2,4,6-trichloro-1,3,5-triazine (TCT) with a catalytic amount of triphenylphosphine as an acid activator. W...
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th-cmuir.6653943832-533292018-09-04T09:47:46Z Solvent-free reduction of carboxylic acids to alcohols with NaBH<inf>4</inf> promoted by 2,4,6-trichloro-1,3,5-triazine and PPh<inf>3</inf> in the presence of K<inf>2</inf>CO<inf>3</inf> Subin Jaita Pantitra Kaewkum Chuthamat Duangkamol Wong Phakhodee Mookda Pattarawarapan Chemical Engineering Chemistry © the Partner Organisations 2014. A simple, rapid, and eco-friendly method for NaBH4 reduction of carboxylic acids to alcohols under solvent-free conditions was developed using a combination of 2,4,6-trichloro-1,3,5-triazine (TCT) with a catalytic amount of triphenylphosphine as an acid activator. With the 1 : 0.2 : 1.5 : 2 mole ratio of TCT : PPh3 : K2CO3 : NaBH4, carboxylic acids including aromatic acids, aliphatic acids, and N-protected α-amino acids (Fmoc, Z) could readily undergo reduction to give the corresponding alcohols in good to excellent yields within 10 min. 2018-09-04T09:47:04Z 2018-09-04T09:47:04Z 2014-01-01 Journal 20462069 2-s2.0-84907647139 10.1039/c4ra08643k https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84907647139&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/53329 |
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Chemical Engineering Chemistry Subin Jaita Pantitra Kaewkum Chuthamat Duangkamol Wong Phakhodee Mookda Pattarawarapan Solvent-free reduction of carboxylic acids to alcohols with NaBH<inf>4</inf> promoted by 2,4,6-trichloro-1,3,5-triazine and PPh<inf>3</inf> in the presence of K<inf>2</inf>CO<inf>3</inf> |
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© the Partner Organisations 2014. A simple, rapid, and eco-friendly method for NaBH4 reduction of carboxylic acids to alcohols under solvent-free conditions was developed using a combination of 2,4,6-trichloro-1,3,5-triazine (TCT) with a catalytic amount of triphenylphosphine as an acid activator. With the 1 : 0.2 : 1.5 : 2 mole ratio of TCT : PPh3 : K2CO3 : NaBH4, carboxylic acids including aromatic acids, aliphatic acids, and N-protected α-amino acids (Fmoc, Z) could readily undergo reduction to give the corresponding alcohols in good to excellent yields within 10 min. |
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Journal |
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Subin Jaita Pantitra Kaewkum Chuthamat Duangkamol Wong Phakhodee Mookda Pattarawarapan |
author_facet |
Subin Jaita Pantitra Kaewkum Chuthamat Duangkamol Wong Phakhodee Mookda Pattarawarapan |
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Subin Jaita |
title |
Solvent-free reduction of carboxylic acids to alcohols with NaBH<inf>4</inf> promoted by 2,4,6-trichloro-1,3,5-triazine and PPh<inf>3</inf> in the presence of K<inf>2</inf>CO<inf>3</inf> |
title_short |
Solvent-free reduction of carboxylic acids to alcohols with NaBH<inf>4</inf> promoted by 2,4,6-trichloro-1,3,5-triazine and PPh<inf>3</inf> in the presence of K<inf>2</inf>CO<inf>3</inf> |
title_full |
Solvent-free reduction of carboxylic acids to alcohols with NaBH<inf>4</inf> promoted by 2,4,6-trichloro-1,3,5-triazine and PPh<inf>3</inf> in the presence of K<inf>2</inf>CO<inf>3</inf> |
title_fullStr |
Solvent-free reduction of carboxylic acids to alcohols with NaBH<inf>4</inf> promoted by 2,4,6-trichloro-1,3,5-triazine and PPh<inf>3</inf> in the presence of K<inf>2</inf>CO<inf>3</inf> |
title_full_unstemmed |
Solvent-free reduction of carboxylic acids to alcohols with NaBH<inf>4</inf> promoted by 2,4,6-trichloro-1,3,5-triazine and PPh<inf>3</inf> in the presence of K<inf>2</inf>CO<inf>3</inf> |
title_sort |
solvent-free reduction of carboxylic acids to alcohols with nabh<inf>4</inf> promoted by 2,4,6-trichloro-1,3,5-triazine and pph<inf>3</inf> in the presence of k<inf>2</inf>co<inf>3</inf> |
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2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84907647139&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/53329 |
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1681424114897649664 |