Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Jumreang Tummatorn"'
Autor:
Supaluk Popruk, Jumreang Tummatorn, Suthasinee Sreesai, Sumate Ampawong, Tipparat Thiangtrongjit, Phornpimon Tipthara, Joel Tarning, Charnsak Thongsornkleeb, Somsak Ruchirawat, Onrapak Reamtong
Publikováno v:
International Journal for Parasitology: Drugs and Drug Resistance, Vol 26, Iss , Pp 100561- (2024)
Giardia duodenalis, a widespread parasitic flagellate protozoan causing giardiasis, affects millions annually, particularly impacting children and travellers. With no effective vaccine available, treatment primarily relies on the oral administration
Externí odkaz:
https://doaj.org/article/365a8d72fd804092913e28ebb5d2ea03
Autor:
Pattaneeya Prangthip, Jumreang Tummatorn, Poom Adisakwattana, Naphatsamon Uthailak, Usa Boonyuen, Phornpimon Tipthara, Joel Tarning, Pavitra Laohapaisan, Charnsak Thongsornkleeb, Somsak Ruchirawat, Onrapak Reamtong
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-13 (2023)
Abstract Parasitic roundworms cause significant sickness and mortality in animals and humans. In livestock, these nematodes have severe economic impact and result in losses in food production on a global scale. None of the currently available drugs i
Externí odkaz:
https://doaj.org/article/6ea568cb3850463eb5bc441b59553465
Autor:
Kitiya Rujimongkon, Mathirut Mungthin, Jumreang Tummatorn, Sumate Ampawong, Poom Adisakwattana, Usa Boonyuen, Onrapak Reamtong
Publikováno v:
PLoS ONE, Vol 14, Iss 8, p e0220871 (2019)
Drug-resistant strains of malaria parasites have emerged for most of antimalarial medications. A new chemotherapeutic compound is needed for malarial therapy. Antimalarial activity against both drug-sensitive and drug-resistant P. falciparum has been
Externí odkaz:
https://doaj.org/article/6cdd728c4750480cad4d058940abbdd3
Autor:
Warabhorn Rodphon, Sutida Linkhum, Charnsak Thongsornkleeb, Jumreang Tummatorn, Somsak Ruchirawat
Publikováno v:
The Journal of Organic Chemistry. 88:4172-4186
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afed165911641b6989b397744eec72ae
https://doi.org/10.1021/acs.joc.2c02664
https://doi.org/10.1021/acs.joc.2c02664
Autor:
Warabhorn Rodphon, Kanokwan Jaithum, Sutida Linkhum, Charnsak Thongsornkleeb, Jumreang Tummatorn, Somsak Ruchirawat
Publikováno v:
The Journal of Organic Chemistry. 88:2677-2691
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f101c70a2bd298a4c5e107a432b2c433
https://doi.org/10.1021/acs.joc.2c00940
https://doi.org/10.1021/acs.joc.2c00940
Autor:
Nitwaree Palavong, Piyaporn Arunkirirote, Jumreang Tummatorn, Charnsak Thongsornkleeb, Somsak Ruchirawat
Publikováno v:
Asian Journal of Organic Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1dd518cc9b71a64de83d2e08be6af4a
https://doi.org/10.1002/ajoc.202300188
https://doi.org/10.1002/ajoc.202300188
Autor:
Kunlayanee Punjajom, Sureeporn Ruengsangtongkul, Jumreang Tummatorn, Praneet Paiboonsombat, Somsak Ruchirawat, Charnsak Thongsornkleeb
Publikováno v:
The Journal of Organic Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f9d5520698e1a29ae6f849a96d42dd5
https://doi.org/10.1021/acs.joc.3c00027
https://doi.org/10.1021/acs.joc.3c00027
Autor:
Charnsak Thongsornkleeb, Sureeporn Ruengsangtongkul, Takahito Kuribara, Nattawadee Chaisan, Jumreang Tummatorn, Somsak Ruchirawat
Publikováno v:
Synlett. 33:1329-1334
Unsymmetrical 1,1,2-triacylalkenes were conveniently prepared by the oxidative coupling of 1,3-keto esters with terminal alkynes by employing 4.0 equivalents of inexpensive ceric ammonium nitrate (CAN) as the oxidant in acetonitrile as the solvent at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5578187714583cb39613d82afb85d949
https://doi.org/10.1055/a-1774-6966
https://doi.org/10.1055/a-1774-6966
Autor:
Charnsak Thongsornkleeb, Nattawadee Chaisan, Sureeporn Ruengsangtongkul, Jumreang Tummatorn, Somsak Ruchirawat
Publikováno v:
Synlett. 33:1426-1430
A mild and convenient method for the synthesis of 2,2-dihaloketones and gem-dihalolactols has been developed. For the synthesis of 2,2-dihaloketones, alkynes were employed as substrates to react with halogenating agents, Cl2 or ClBr, that were genera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7fff9f26d224ad576e51c58be3f1704
https://doi.org/10.1055/a-1774-7077
https://doi.org/10.1055/a-1774-7077
Publikováno v:
The Journal of organic chemistry. 87(22)
In this work, a synthetic method for the synthesis of 2,3-dihydronaphtho[1,2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1eced5dbeb35be0cdd7960327b8a927c
https://pubmed.ncbi.nlm.nih.gov/36282245
https://pubmed.ncbi.nlm.nih.gov/36282245