Preparation of Mesoporous SBA-16 Silica-Supported Biscinchona Alkaloid Ligand for the Asymmetric Dihydroxylation of Olefins
Optically active cinchona alkaloid was anchored onto mesoporous SBA-16 silica and the as-prepared complex was used as a heterogeneous chiral ligand of osmium tetraoxide for the asymmetric dihydroxylation of olefins. The prepared catalytic system provided 90–93% yield of vicinal diol with 92–99% enan...
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Hindawi Publishing Corporation
2014
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ump-61312018-02-14T04:10:59Z http://umpir.ump.edu.my/id/eprint/6131/ Preparation of Mesoporous SBA-16 Silica-Supported Biscinchona Alkaloid Ligand for the Asymmetric Dihydroxylation of Olefins Sarkar, Shaheen M. Md. Eaqub, Ali Lutfor, M. R. M. M., Yusoff QD Chemistry Optically active cinchona alkaloid was anchored onto mesoporous SBA-16 silica and the as-prepared complex was used as a heterogeneous chiral ligand of osmium tetraoxide for the asymmetric dihydroxylation of olefins. The prepared catalytic system provided 90–93% yield of vicinal diol with 92–99% enantioselectivity. The ordered mesoporous SBA-16 silica was found to be a valuable support for the cinchona alkaloid liganded osmium catalyst system which is frequently used in chemical industries and research laboratories for olefin functionalization. Hindawi Publishing Corporation 2014 Article PeerReviewed application/pdf en http://umpir.ump.edu.my/id/eprint/6131/1/Preparation_of_Mesoporous_SBA-16_Silica-Supported_Biscinchona_Alkaloid_Ligand_for_the_Asymmetric_Dihydroxylation_of_Olefins.pdf Sarkar, Shaheen M. and Md. Eaqub, Ali and Lutfor, M. R. and M. M., Yusoff (2014) Preparation of Mesoporous SBA-16 Silica-Supported Biscinchona Alkaloid Ligand for the Asymmetric Dihydroxylation of Olefins. Journal of Nanomaterials, 2014. pp. 1-5. ISSN 1687-4110 (print); 1687-4129 (online) http://dx.doi.org/10.1155/2014/123680 DOI: 10.1155/2014/123680 |
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QD Chemistry Sarkar, Shaheen M. Md. Eaqub, Ali Lutfor, M. R. M. M., Yusoff Preparation of Mesoporous SBA-16 Silica-Supported Biscinchona Alkaloid Ligand for the Asymmetric Dihydroxylation of Olefins |
description |
Optically active cinchona alkaloid was anchored onto mesoporous SBA-16 silica and the as-prepared complex was used as a heterogeneous chiral ligand of osmium tetraoxide for the asymmetric dihydroxylation of olefins. The prepared catalytic system provided 90–93% yield of vicinal diol with 92–99% enantioselectivity. The ordered mesoporous SBA-16 silica was found to be a valuable support for the cinchona alkaloid liganded osmium catalyst system which is frequently used in chemical industries and research laboratories for olefin functionalization. |
format |
Article |
author |
Sarkar, Shaheen M. Md. Eaqub, Ali Lutfor, M. R. M. M., Yusoff |
author_facet |
Sarkar, Shaheen M. Md. Eaqub, Ali Lutfor, M. R. M. M., Yusoff |
author_sort |
Sarkar, Shaheen M. |
title |
Preparation of Mesoporous SBA-16 Silica-Supported Biscinchona Alkaloid Ligand for the Asymmetric Dihydroxylation of Olefins |
title_short |
Preparation of Mesoporous SBA-16 Silica-Supported Biscinchona Alkaloid Ligand for the Asymmetric Dihydroxylation of Olefins |
title_full |
Preparation of Mesoporous SBA-16 Silica-Supported Biscinchona Alkaloid Ligand for the Asymmetric Dihydroxylation of Olefins |
title_fullStr |
Preparation of Mesoporous SBA-16 Silica-Supported Biscinchona Alkaloid Ligand for the Asymmetric Dihydroxylation of Olefins |
title_full_unstemmed |
Preparation of Mesoporous SBA-16 Silica-Supported Biscinchona Alkaloid Ligand for the Asymmetric Dihydroxylation of Olefins |
title_sort |
preparation of mesoporous sba-16 silica-supported biscinchona alkaloid ligand for the asymmetric dihydroxylation of olefins |
publisher |
Hindawi Publishing Corporation |
publishDate |
2014 |
url |
http://umpir.ump.edu.my/id/eprint/6131/ http://umpir.ump.edu.my/id/eprint/6131/ http://umpir.ump.edu.my/id/eprint/6131/ http://umpir.ump.edu.my/id/eprint/6131/1/Preparation_of_Mesoporous_SBA-16_Silica-Supported_Biscinchona_Alkaloid_Ligand_for_the_Asymmetric_Dihydroxylation_of_Olefins.pdf |
first_indexed |
2023-09-18T22:01:38Z |
last_indexed |
2023-09-18T22:01:38Z |
_version_ |
1777414437427216384 |