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- W2951766712 abstract "A convenient and efficient methodology for the head-to-tail macrocyclization of small 3-mer, 4-mer, and 5-mer α-peptoid acids (9-, 12-, and 15-atom N-substituted glycine oligomers) is described. The cyclic trimer has a ccc amide sequence in the crystal structure, whereas the tetramer has ctct and the pentamer has ttccc stereochemistry. NMR analysis reveals rigid structures in solution. These synthetic macrocycles may prove useful in medicinal and materials applications." @default.
- W2951766712 created "2019-06-27" @default.
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- W2951766712 date "2014-05-05" @default.
- W2951766712 modified "2023-09-24" @default.
- W2951766712 title "Small Head-to-Tail Macrocyclic α-Peptoids" @default.
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- W2951766712 doi "https://doi.org/10.1021/ol501102b" @default.
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