Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Chonchanok Buathongjan"'
Autor:
Kamolwan Israkarn, Chonchanok Buathongjan, Chaiwut Gamonpilas, Pawadee Methacanon, Sirikarn Wisetsuwannaphum
Publikováno v:
Journal of food scienceREFERENCES. 87(11)
In this study, the effects of gellan gum types and CaCl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2ee46c9ef03e5ffe670e89028d91b7b
https://pubmed.ncbi.nlm.nih.gov/36181362
https://pubmed.ncbi.nlm.nih.gov/36181362
Publikováno v:
Comprehensive reviews in food science and food safetyREFERENCES. 20(4)
In today's market environment, an aging society is recognized as one of the megatrends in the world. The demographic change in the world population age structure has driven a huge demand in healthcare products as well as services that include the tec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d60935b17661bba4f89b85d2300e6638
https://pubmed.ncbi.nlm.nih.gov/34146451
https://pubmed.ncbi.nlm.nih.gov/34146451
Autor:
Chaiwut Gamonpilas, Kamolwan Israkarn, Théo Outrequin, Watchara Sangwan, Chonchanok Buathongjan, Pawadee Methacanon
Publikováno v:
International journal of biological macromolecules. 164
Although synthetic antioxidant food additives are widely used in a variety of food products, some of them are suspected of having a noxious effect on human health. As a consequence, much research attention has been focused on developing natural antio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33cca16cbffe9f254deb1e9776b20f5a
https://pubmed.ncbi.nlm.nih.gov/32941910
https://pubmed.ncbi.nlm.nih.gov/32941910
Publikováno v:
European Journal of Organic Chemistry. 2017:1025-1032
A highly efficient iodine/TBHP-mediated one-pot deoxygenative and regioselective C2-sulfonylation of quinoline N-oxides with sodium sulfinate salts has been developed. This metal, base and phosphorus-free protocol employs readily accessible and easy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::428facf656ce83c2932e205a26b3b48b
https://doi.org/10.1002/ejoc.201601443
https://doi.org/10.1002/ejoc.201601443
Publikováno v:
European Journal of Organic Chemistry. 2015:1575-1582
The iodine-catalyzed oxidative amination of sodium sulfinates in the presence of sodium percarbonate as the oxidant has been developed. The reaction shows good substrate scope and tolerates a wide range of functionalities in both amine and sodium sul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eead4ac2c64b667bb99f353c75b28623
https://doi.org/10.1002/ejoc.201403531
https://doi.org/10.1002/ejoc.201403531
Autor:
Danupat Beukeaw, Chonchanok Buathongjan, Ladawan Sumunnee, Vichai Reutrakul, Sirilata Yotphan
Publikováno v:
ChemInform. 47
A new protocol for the synthesis of sulfonamides via an iodine-catalyzed sulfonylation of amines with sulfonyl hydrazides is developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7ff5fee50d5df4375664da155e59b61
https://doi.org/10.1002/chin.201620067
https://doi.org/10.1002/chin.201620067
Autor:
Chonchanok Buathongjan, Ladawan Sumunnee, Danupat Beukeaw, Sirilata Yotphan, Vichai Reutrakul
Publikováno v:
Organicbiomolecular chemistry. 14(2)
A new synthesis of sulfonamides has been developed via an iodine-catalyzed sulfonylation of amines with arylsulfonyl hydrazides. This metal-free strategy employs readily accessible and easy to handle starting materials, catalysts and oxidants, and ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0be262147b33a70adfec4f8f27d3c13
https://pubmed.ncbi.nlm.nih.gov/26531097
https://pubmed.ncbi.nlm.nih.gov/26531097
Publikováno v:
ChemInform. 46
The reaction is tolerant to a wide range of functional groups in both partners and affords sulfonamides in moderate to good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4edb2b200655ff62f25c03eaa858e7d2
https://doi.org/10.1002/chin.201526106
https://doi.org/10.1002/chin.201526106