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Self-assembly of chiral BINOL cages imine condensation
Condensation of an ( S )- or ( R )-BINOL-derived dialdehyde and tris(2-aminoethyl)amine produced chiral [2+3] imine cages, which were further reduced to furnish more stable chiral amine cages and applied in the enantioselective recognition of (1 R ,2 R )- and (1 S ,2 S )-1,2-diaminocyclohexane. Chir...
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| Published in: | Chemical communications (Cambridge, England) England), 2021-09, Vol.57 (72), p.988-991 |
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| Main Authors: | , , , , , , |
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| container_end_page | 991 |
| container_issue | 72 |
| container_start_page | 988 |
| container_title | Chemical communications (Cambridge, England) |
| container_volume | 57 |
| creator | Ramakrishna, E Tang, Jia-Dong Tao, Jia-Ju Fang, Qiang Zhang, Zibin Huang, Jianying Li, Shijun |
| description | Condensation of an (
S
)- or (
R
)-BINOL-derived dialdehyde and tris(2-aminoethyl)amine produced chiral [2+3] imine cages, which were further reduced to furnish more stable chiral amine cages and applied in the enantioselective recognition of (1
R
,2
R
)- and (1
S
,2
S
)-1,2-diaminocyclohexane.
Chiral [2+3] imine cages were constructed
via
imine condensation from an enantiomeric pair of BINOL-derived dialdehydes and tris(2-aminoethyl)amine and applied in the enantioselective recognition of (1
R
,2
R
)- and (1
S
,2
S
)-1,2-diaminocyclohexane. |
| doi_str_mv | 10.1039/d1cc01507a |
| format | article |
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S
)- or (
R
)-BINOL-derived dialdehyde and tris(2-aminoethyl)amine produced chiral [2+3] imine cages, which were further reduced to furnish more stable chiral amine cages and applied in the enantioselective recognition of (1
R
,2
R
)- and (1
S
,2
S
)-1,2-diaminocyclohexane.
Chiral [2+3] imine cages were constructed
via
imine condensation from an enantiomeric pair of BINOL-derived dialdehydes and tris(2-aminoethyl)amine and applied in the enantioselective recognition of (1
R
,2
R
)- and (1
S
,2
S
)-1,2-diaminocyclohexane.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/d1cc01507a</identifier><ispartof>Chemical communications (Cambridge, England), 2021-09, Vol.57 (72), p.988-991</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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>Ramakrishna, E</creatorcontrib><creatorcontrib>Tang, Jia-Dong</creatorcontrib><creatorcontrib>Tao, Jia-Ju</creatorcontrib><creatorcontrib>Fang, Qiang</creatorcontrib><creatorcontrib>Zhang, Zibin</creatorcontrib><creatorcontrib>Huang, Jianying</creatorcontrib><creatorcontrib>Li, Shijun</creatorcontrib><title>Self-assembly of chiral BINOL cages imine condensation</title><title>Chemical communications (Cambridge, England)</title><description>Condensation of an (
S
)- or (
R
)-BINOL-derived dialdehyde and tris(2-aminoethyl)amine produced chiral [2+3] imine cages, which were further reduced to furnish more stable chiral amine cages and applied in the enantioselective recognition of (1
R
,2
R
)- and (1
S
,2
S
)-1,2-diaminocyclohexane.
Chiral [2+3] imine cages were constructed
via
imine condensation from an enantiomeric pair of BINOL-derived dialdehydes and tris(2-aminoethyl)amine and applied in the enantioselective recognition of (1
R
,2
R
)- and (1
S
,2
S
)-1,2-diaminocyclohexane.</description><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNpjYBAyNNAzNDC21E8xTE42MDQ1ME9kYuA0NDYz0TU1sYhgAbFNLXXNjU1MORi4iouzDIDA0NSCk8EsODUnTTexuDg1NymnUiE_TSE5I7MoMUfBydPP30chOTE9tVghMzczL1UhOT8vJTWvOLEkMz-Ph4E1LTGnOJUXSnMzyLq5hjh76BYVJ8cXFGXmJhZVxiMcY0xIHgAHQjaE</recordid><startdate>20210909</startdate><enddate>20210909</enddate><creator>Ramakrishna, E</creator><creator>Tang, Jia-Dong</creator><creator>Tao, Jia-Ju</creator><creator>Fang, Qiang</creator><creator>Zhang, Zibin</creator><creator>Huang, Jianying</creator><creator>Li, Shijun</creator><scope/></search><sort><creationdate>20210909</creationdate><title>Self-assembly of chiral BINOL cages imine condensation</title><author>Ramakrishna, E ; Tang, Jia-Dong ; Tao, Jia-Ju ; Fang, Qiang ; Zhang, Zibin ; Huang, Jianying ; Li, Shijun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_d1cc01507a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><creationdate>2021</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Ramakrishna, E</creatorcontrib><creatorcontrib>Tang, Jia-Dong</creatorcontrib><creatorcontrib>Tao, Jia-Ju</creatorcontrib><creatorcontrib>Fang, Qiang</creatorcontrib><creatorcontrib>Zhang, Zibin</creatorcontrib><creatorcontrib>Huang, Jianying</creatorcontrib><creatorcontrib>Li, Shijun</creatorcontrib><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ramakrishna, E</au><au>Tang, Jia-Dong</au><au>Tao, Jia-Ju</au><au>Fang, Qiang</au><au>Zhang, Zibin</au><au>Huang, Jianying</au><au>Li, Shijun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Self-assembly of chiral BINOL cages imine condensation</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><date>2021-09-09</date><risdate>2021</risdate><volume>57</volume><issue>72</issue><spage>988</spage><epage>991</epage><pages>988-991</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>Condensation of an (
S
)- or (
R
)-BINOL-derived dialdehyde and tris(2-aminoethyl)amine produced chiral [2+3] imine cages, which were further reduced to furnish more stable chiral amine cages and applied in the enantioselective recognition of (1
R
,2
R
)- and (1
S
,2
S
)-1,2-diaminocyclohexane.
Chiral [2+3] imine cages were constructed
via
imine condensation from an enantiomeric pair of BINOL-derived dialdehydes and tris(2-aminoethyl)amine and applied in the enantioselective recognition of (1
R
,2
R
)- and (1
S
,2
S
)-1,2-diaminocyclohexane.</abstract><doi>10.1039/d1cc01507a</doi><tpages>4</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1359-7345 |
| ispartof | Chemical communications (Cambridge, England), 2021-09, Vol.57 (72), p.988-991 |
| issn | 1359-7345 1364-548X |
| language | |
| recordid | cdi_rsc_primary_d1cc01507a |
| source | Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list) |
| title | Self-assembly of chiral BINOL cages imine condensation |
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