Efficient magnetic and recyclable SBILC (supported basic ionic liquid catalyst)-based heterogeneous organocatalysts for the asymmetric epoxidation of trans-methylcinnamate
A green alternative, based on the use of an efficient and recyclable chiral ketone@SBILC@MWCNT@Fe 3 O 4 catalytic system ( Y = 35%, S = 100% and ee = 100%), was developed for the asymmetric epoxidation of trans -methylcinnamate to (2 R ,3 S )-phenyl glycidate. A green heterogeneous catalytic alterna...
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| Veröffentlicht in: | Catalysis science & technology 2015-01, Vol.5 (2), p.729-737 |
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| container_title | Catalysis science & technology |
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| creator | Candu, N Rizescu, C Podolean, I Tudorache, M Parvulescu, V. I Coman, S. M |
| description | A green alternative, based on the use of an efficient and recyclable chiral ketone@SBILC@MWCNT@Fe
3
O
4
catalytic system (
Y
= 35%,
S
= 100% and ee = 100%), was developed for the asymmetric epoxidation of
trans
-methylcinnamate to (2
R
,3
S
)-phenyl glycidate.
A green heterogeneous catalytic alternative was developed for the asymmetric epoxidation of
trans
-methylcinnamate to (2
R
,3
S
)-phenyl glycidate. |
| doi_str_mv | 10.1039/c4cy00891j |
| format | Article |
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3
O
4
catalytic system (
Y
= 35%,
S
= 100% and ee = 100%), was developed for the asymmetric epoxidation of
trans
-methylcinnamate to (2
R
,3
S
)-phenyl glycidate.
A green heterogeneous catalytic alternative was developed for the asymmetric epoxidation of
trans
-methylcinnamate to (2
R
,3
S
)-phenyl glycidate.</description><identifier>ISSN: 2044-4753</identifier><identifier>EISSN: 2044-4761</identifier><identifier>DOI: 10.1039/c4cy00891j</identifier><language>eng</language><ispartof>Catalysis science & technology, 2015-01, Vol.5 (2), p.729-737</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-6466e5d4c1769b9bd850210238b1fb1f55f1d9d6975b17d23e2a0df9e7158d9d3</citedby><cites>FETCH-LOGICAL-c316t-6466e5d4c1769b9bd850210238b1fb1f55f1d9d6975b17d23e2a0df9e7158d9d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Candu, N</creatorcontrib><creatorcontrib>Rizescu, C</creatorcontrib><creatorcontrib>Podolean, I</creatorcontrib><creatorcontrib>Tudorache, M</creatorcontrib><creatorcontrib>Parvulescu, V. I</creatorcontrib><creatorcontrib>Coman, S. M</creatorcontrib><title>Efficient magnetic and recyclable SBILC (supported basic ionic liquid catalyst)-based heterogeneous organocatalysts for the asymmetric epoxidation of trans-methylcinnamate</title><title>Catalysis science & technology</title><description>A green alternative, based on the use of an efficient and recyclable chiral ketone@SBILC@MWCNT@Fe
3
O
4
catalytic system (
Y
= 35%,
S
= 100% and ee = 100%), was developed for the asymmetric epoxidation of
trans
-methylcinnamate to (2
R
,3
S
)-phenyl glycidate.
A green heterogeneous catalytic alternative was developed for the asymmetric epoxidation of
trans
-methylcinnamate to (2
R
,3
S
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3
O
4
catalytic system (
Y
= 35%,
S
= 100% and ee = 100%), was developed for the asymmetric epoxidation of
trans
-methylcinnamate to (2
R
,3
S
)-phenyl glycidate.
A green heterogeneous catalytic alternative was developed for the asymmetric epoxidation of
trans
-methylcinnamate to (2
R
,3
S
)-phenyl glycidate.</abstract><doi>10.1039/c4cy00891j</doi><tpages>9</tpages></addata></record> |
| fulltext | fulltext |
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| ispartof | Catalysis science & technology, 2015-01, Vol.5 (2), p.729-737 |
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| source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
| title | Efficient magnetic and recyclable SBILC (supported basic ionic liquid catalyst)-based heterogeneous organocatalysts for the asymmetric epoxidation of trans-methylcinnamate |
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