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Data · collection · 2015

Covalently assembled resorcin[4]arenes and molecular tweezers: a chiral recognition rationale by NMR

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Chiral diamides and tetramidic resorcin[4]arenes deriving from ( R , R )-1,2-diaminocyclohexane and ( S , S )-1,2-diphenylethylendiamine, and a valine containing resorcin[4]arene have been compared by NMR in the enantiodiscrimination of mandelic acid.

Description

The relevance of cooperation between side arms and external surface of resorcin[4]arene core has been ascertained.

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Provenance · 1 source records, 11 field assertions
SourceKeyLast seenRaw
DataCite10.6084/m9.figshare.c.2128082.v113 d agoJSON v1
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access_levelsource · DataCiteconnector:datacite@1.0.0/data/attributes/rightsList
concepts[disease].local:disease:cancermapping · DataCitevocabulary-mapper@1.0.0keywords['Cancer']
concepts[field].fos:biological-sciencessource · DataCiteconnector:datacite@1.0.0
concepts[field].fos:chemical-sciencessource · DataCiteconnector:datacite@1.0.0
concepts[field].fos:mathematicssource · DataCiteconnector:datacite@1.0.0
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