Oxetanyl Peptides: Novel Peptidomimetic Modules for Medicinal Chemistry
Publication type: Journal Article
Publication date: 2014-07-28
scimago Q1
wos Q1
SJR: 1.235
CiteScore: 8.7
Impact factor: 5.0
ISSN: 15237060, 15237052
PubMed ID:
25068485
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
The synthesis of novel oxetanyl peptides, where the amide bond is replaced by a non-hydrolyzable oxetanylamine fragment, is reported. This new class of pseudo-dipeptides with the same H-bond donor/acceptor pattern found in proteins expands the repertoire of peptidomimetics.
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Metrics
65
Total citations:
65
Citations from 2025:
3
(4.62%)
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MLA
Cite this
GOST
Copy
McLaughlin M. et al. Oxetanyl Peptides: Novel Peptidomimetic Modules for Medicinal Chemistry // Organic Letters. 2014. Vol. 16. No. 16. pp. 4070-4073.
GOST all authors (up to 50)
Copy
McLaughlin M., Ohshima T., Fessard T. C., Miller S. Oxetanyl Peptides: Novel Peptidomimetic Modules for Medicinal Chemistry // Organic Letters. 2014. Vol. 16. No. 16. pp. 4070-4073.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1021/ol501590n
UR - https://doi.org/10.1021/ol501590n
TI - Oxetanyl Peptides: Novel Peptidomimetic Modules for Medicinal Chemistry
T2 - Organic Letters
AU - McLaughlin, Martin
AU - Ohshima, Takashi
AU - Fessard, Thomas C.
AU - Miller, Scott
PY - 2014
DA - 2014/07/28
PB - American Chemical Society (ACS)
SP - 4070-4073
IS - 16
VL - 16
PMID - 25068485
SN - 1523-7060
SN - 1523-7052
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2014_McLaughlin,
author = {Martin McLaughlin and Takashi Ohshima and Thomas C. Fessard and Scott Miller},
title = {Oxetanyl Peptides: Novel Peptidomimetic Modules for Medicinal Chemistry},
journal = {Organic Letters},
year = {2014},
volume = {16},
publisher = {American Chemical Society (ACS)},
month = {jul},
url = {https://doi.org/10.1021/ol501590n},
number = {16},
pages = {4070--4073},
doi = {10.1021/ol501590n}
}
Cite this
MLA
Copy
McLaughlin, Martin, et al. “Oxetanyl Peptides: Novel Peptidomimetic Modules for Medicinal Chemistry.” Organic Letters, vol. 16, no. 16, Jul. 2014, pp. 4070-4073. https://doi.org/10.1021/ol501590n.