Facile formation of chiral calixarene analogs incorporating cystine peptide into the macrocyclic ring.
نویسندگان
چکیده
Chiral calixarene analogs incorporating cystine peptide into their macrocyclic ring were easily prepared by the cyclization reactions of bis(chloromethyl)phenol-formaldehyde oligomers with cystine peptides in moderate yields. Circular dichroism (CD) spectra indicated the existence of the transmission of the chirality from peptide unit to phenol-formaldehyde oligomer moiety.
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ورودعنوان ژورنال:
- Chemical & pharmaceutical bulletin
دوره 50 3 شماره
صفحات -
تاریخ انتشار 2002