Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Courtney M. O'Farrell"'
Publikováno v:
Chirality. 21:911-921
Water-soluble calix[4]resorcinarenes with proline, 3-hydroxyproline, and 4-hydroxyproline substituent groups are evaluated as chiral NMR solvating agents on a series of bicyclic aromatic compounds with naphthyl, indole, dihydroindole, and indane ring
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2ad35dc54484121d060a1a8d7548a9b
https://doi.org/10.1002/chir.20688
https://doi.org/10.1002/chir.20688
Publikováno v:
European Journal of Organic Chemistry. 2009:4825-4832
A series of water-soluble sulfonated calix[4]resorcinarenes with L-proline, cis-4-hydroxy-d- and -L-proline, trans-4-hydroxy-L-proline and trans-3-hydroxy-L-proline are evaluated as chiral NMR solvating agents. The changes in chemical shifts and enan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::239a2bae0d8ac09967c3e38a192752bd
https://doi.org/10.1002/ejoc.200900674
https://doi.org/10.1002/ejoc.200900674
Publikováno v:
Tetrahedron: Asymmetry. 19:1790-1796
Water-soluble calix[4]resorcinarenes with 3- and 4-hydroxyproline substituent groups are evaluated as chiral NMR solvating agents on a series of monosubstituted phenyl-containing compounds. The substrates interact with the calixresorcinarene through
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8875cca2b68f8c1b85d16e38cebe7082
https://doi.org/10.1016/j.tetasy.2008.07.023
https://doi.org/10.1016/j.tetasy.2008.07.023
Autor:
Jan M. Collins, Thomas J. Wenzel, J. Matthew Chudomel, Courtney M. O'Farrell, Catherine F. Dignam
Publikováno v:
The Journal of organic chemistry. 73(7)
Water-soluble calix[4]resorcinarenes containing 3- and 4-hydroxyproline, d-nipecotic acid, (S)-2-(methoxymethyl)pyrrolidine, (S)-2-pyrrolidine methanol, and (S,S)-(+)-2,4-bis(methoxymethyl)pyrrolidine substituents are synthesized and evaluated as chi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb2f8b6898a374f5d4a3c2a6157465fd
https://pubmed.ncbi.nlm.nih.gov/18336044
https://pubmed.ncbi.nlm.nih.gov/18336044