Journal
CHIRALITY
Volume 34, Issue 11, Pages 1466-1471Publisher
WILEY
DOI: 10.1002/chir.23503
Keywords
calix[4]arene acetic acids; chiral amides; diastereomers; inherent chirality; separation
Funding
- National Academy of Sciences of Ukraine [0118U006190]
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A preparative method for synthesizing optically pure N-(1-phenylethyl)amides of inherently chiral (cR)- and (cS)-dibenzoyloxy-calix[4]arene acetic acids has been developed, and their absolute stereochemical configuration was determined by X-ray diffraction analysis.
A preparative method for the synthesis of optically pure N-(1-phenylethyl)amides of inherently chiral (cR)- and (cS)-dibenzoyloxy-calix[4]arene acetic acids has been developed. Their absolute stereochemical configuration was determined by X-ray diffraction analysis.
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