Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ankur Jalan"'
Autor:
Jingyao Wang, Mark R. Berglund, Timothy Braden, Matthew C. Embry, Martin D. Johnson, Stephen R. Groskreutz, Fareed Bhasha Sayyed, Sergey Vladimirovich Tsukanov, Timothy D. White, Ankur Jalan, Kevin D. Seibert, Michael E. Kopach
Publikováno v:
ACS Omega, Vol 7, Iss 50, Pp 46809-46824 (2022)
Externí odkaz:
https://doaj.org/article/0d36177179bf4c10b430c4f3e285bf18
Autor:
Mark A. Strege, Trent J. Oman, Donald S. Risley, Laura K. Muehlbauer, Ankur Jalan, Zhirui Jerry Lian
Publikováno v:
Journal of Chromatography B. 1219:123638
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1dca9c0d736fdc1dc05e6caa85a3c30
https://doi.org/10.1016/j.jchromb.2023.123638
https://doi.org/10.1016/j.jchromb.2023.123638
Autor:
Shi Luo, Joseph M. Cardon, Concordia C. L. Lo, Zhiwei Ma, Diego A. Moyá, Yu Cai, Ankur Jalan, Jintao Jiang, Daniel Joaquin, Alexander Ramos, Steven L. Castle
Publikováno v:
Angew Chem Int Ed Engl
Total synthesis of the anticancer peptide natural product yaku'amide A is reported. Its β-tert-hydroxy amino acids were prepared by regioselective aminohydroxylation involving a chiral mesyloxycarbamate reagent. Stereospecific construction of the E-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1de5a3c2c3a5bbcb4fd7c4b4255be756
https://doi.org/10.1002/ange.202014238
https://doi.org/10.1002/ange.202014238
Publikováno v:
Proceedings of the 35th European Peptide Symposium.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c06172a618741076d35e665c9ca2f72f
https://doi.org/10.17952/35eps.2018.180
https://doi.org/10.17952/35eps.2018.180
Publikováno v:
Organic Letters. 17:488-491
Microwave-promoted iminyl radical cyclizations can be terminated by trapping with TEMPO, affording functionalized adducts. The use of alkynes as radical acceptors delivers a range of 2-acylpyrroles in good yields. Toxic and hazardous reagents, which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4cef27af49709457a28eba89fdd42e0
https://doi.org/10.1021/ol5035047
https://doi.org/10.1021/ol5035047
Publikováno v:
Organic letters. 19(19)
The bulky dehydroamino acids dehydrovaline (ΔVal) and dehydroethylnorvaline (ΔEnv) can be inserted into the turn regions of β-hairpin peptides without altering their secondary structures. These residues increase proteolytic stability, with ΔVal a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8acf2384bfa43d32233846a2765e9af
https://pubmed.ncbi.nlm.nih.gov/28910115
https://pubmed.ncbi.nlm.nih.gov/28910115
Publikováno v:
2017 IEEE International Conference on Power, Control, Signals and Instrumentation Engineering (ICPCSI).
The visually impaired, in their daily lives face innumerable challenges. Amongst which, the ability to independently navigate and perform daily tasks are the most highly affected activities. This approach is based on the abilities of utilizing visual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e81ef9304292d651b41570ffdce91883
https://doi.org/10.1109/icpcsi.2017.8392263
https://doi.org/10.1109/icpcsi.2017.8392263
Publikováno v:
Tetrahedron Letters. 56:3311-3313
Methods of incorporating bulky α,β-dehydroamino acids such as dehydrovaline and dehydroethylnorvaline into peptides via solid-phase peptide synthesis and the resulting peptide compositions is reported. The synthesis method involves using azlactone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbcfc14c9cc5a1d085c1b92ce92d76b1
https://doi.org/10.1016/j.tetlet.2014.12.097
https://doi.org/10.1016/j.tetlet.2014.12.097
Publikováno v:
ChemInform. 46
The mild protocol does not require toxic or hazardous reagents and tolerates a variety of functional groups including acid and base labile ones.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c37c6568e0ad99a28844501e2382ed58
https://doi.org/10.1002/chin.201525148
https://doi.org/10.1002/chin.201525148