Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Satsawat Visansirikul"'
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 9, p 7870 (2023)
Charantin is a mixture of β-sitosterol and stigmastadienol glucosides, which effectively lowers high blood glucose. Novel molecularly imprinted polymers coated magnetic nanoparticles (Fe3O4@MIPs) and filter paper (paper@MIPs) were synthesized by sol
Externí odkaz:
https://doaj.org/article/09eb69ac699a4cca8f08a57b2f3eb2e7
Publikováno v:
Journal of Carbohydrate Chemistry. 39:301-333
To enhance our understanding of the activation and conjugation processes, reported herein is the synthesis of oligosaccharides comprising two sequential repeating units of capsular polysaccharide S...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd2b9d8c92d11e1af11a26289ee042a8
https://doi.org/10.1080/07328303.2020.1821042
https://doi.org/10.1080/07328303.2020.1821042
Publikováno v:
Organic & Biomolecular Chemistry. 18:6682-6695
O-Picoloyl protecting groups at remote positions can affect the stereoselectivity of glycosylation by means of the H-bond-mediated aglycone delivery (HAD) pathway. A new practical method for the stereoselective synthesis of β-glycosides of mannosami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30ce618755f46c84b48e31bbb8d0a441
https://doi.org/10.1039/d0ob01640c
https://doi.org/10.1039/d0ob01640c
Publikováno v:
Pharmaceutical Sciences Asia. 47:310-318
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a35cbef9c64092f6ba6457a30bf283b
https://doi.org/10.29090/psa.2020.04.020.0058
https://doi.org/10.29090/psa.2020.04.020.0058
Autor:
Jiradanai Sarasamkan, Satsawat Visansirikul, Khajornkiat Srichachet, Kittisak Sripha, Opa Vajragupta
Publikováno v:
Nuclear Medicine and Biology. :S156-S157
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f79cf6b0e5b11f859e41dda988e9afa
https://doi.org/10.1016/s0969-8051(22)00333-x
https://doi.org/10.1016/s0969-8051(22)00333-x
Publikováno v:
The Journal of Organic Chemistry. 84:216-227
To gain a better understanding of the conjugation chemistry taking place at the interface of the capsular polysaccharide repeating units, described herein is the synthesis of two disaccharides. These disaccharides correspond to the connection point o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e9d13a407b38899a31125fbb6803bde
https://doi.org/10.1021/acs.joc.8b02612
https://doi.org/10.1021/acs.joc.8b02612
Publikováno v:
Organicbiomolecular chemistry. 19(12)
Reported herein is a new method for a highly effective synthesis of β-glycosides from mannuronic acid donors equipped with the 3-O-picoloyl group. The stereocontrol of glycosylations was achieved by means of the H-bond-mediated aglycone delivery (HA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::028c022fad474df40836cfe2e81c85ac
https://pubmed.ncbi.nlm.nih.gov/33687051
https://pubmed.ncbi.nlm.nih.gov/33687051
Publikováno v:
Organicbiomolecular chemistry. 18(5)
The S. aureus bacterium is surrounded by capsular polysaccharides. These capsular polysaccharides are important in the pathogenesis of staphylococcal infection. There are 11 serotypes of capsular polysaccharides that have been identified, and a major
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97b847379e34a45eeca72002c822ba97
https://pubmed.ncbi.nlm.nih.gov/31922180
https://pubmed.ncbi.nlm.nih.gov/31922180
Autor:
Yongzhen Zhang, Jeroen D. C. Codée, Satsawat Visansirikul, Catherine Alex, Alexei V. Demchenko, Jagodige P. Yasomanee
Publikováno v:
Carbohydrate Research, 488
Carbohydr Res
Carbohydr Res
Reported herein is the synthesis of a number of building blocks of 2-amino-2-deoxy-d-mannose from common d-glucose precursors.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19ae440a56caf232eb84feefd5f0fc51
https://hdl.handle.net/1887/3200445
https://hdl.handle.net/1887/3200445
Publikováno v:
Russian Chemical Bulletin. 64:1107-1118
Described herein is the synthesis and evaluation of a series of glycosyl donors equipped with halobenzoyl substituents at O(4) and O(6) to study their properties in glycosylations. Among possible effects that may include carbonyl participation or H-b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6253ba8fe90988563454fdac82c8f75
https://doi.org/10.1007/s11172-015-0987-2
https://doi.org/10.1007/s11172-015-0987-2