Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Poramate Songthammawat"'
Autor:
Jitra Limthongkul, Kornkamon Akkarasereenon, Tanpitcha Yodweerapong, Poramate Songthammawat, Pirut Tong-Ngam, Alisa Tubsuwan, Nawapol Kunkaew, Phongthon Kanjanasirirat, Tanawadee Khumpanied, Warawuth Wannalo, Sukathida Ubol, Suparerk Borwornpinyo, Poonsakdi Ploypradith, Marisa Ponpuak
Publikováno v:
Viruses, Vol 15, Iss 10, p 2012 (2023)
Every year, dengue virus (DENV) affects millions of people. Currently, there are no approved drugs for the treatment of DENV infection. Autophagy is a conserved degradation process that was shown to be induced by DENV infection and required for optim
Externí odkaz:
https://doaj.org/article/574b446204a343a58ec3c8ec0ae84934
Publikováno v:
Synlett. 33:1312-1316
By starting from two simple building blocks, benzannulated cyclooctenones were obtained in three steps. Subsequent Grignard/aryl lithium addition to the ketone yielded the corresponding tertiary alcohols that underwent stereoselective acid-catalyzed
Publikováno v:
The Journal of organic chemistry. 87(1)
Palodesangrens A and C along with the common tetracyclic core are prepared from simple benzaldehyde and acetophenone derivatives in a 10-step longest linear sequence which featured the Diels-Alder reaction forming the cyclohexene moiety, LiAlH
Autor:
Paratchata Batsomboon, Poonsakdi Ploypradith, Jira Jongcharoenkamol, Somsak Ruchirawat, Poramate Songthammawat, Tanawat Phumjan
Publikováno v:
The Journal of organic chemistry. 86(19)
Starting from benzaldehyde derivatives, the corresponding dibenzocycloheptenol could be prepared in five steps. Under both substrate (secondary vs tertiary alcohol and the substituents on the aromatic ring(s)) and condition control, the subsequent ep
Autor:
Poonsakdi Ploypradith, Somsak Ruchirawat, Kassrin Tangdenpaisal, Kornkamon Akkarasereenon, Poramate Songthammawat, Kanokpish Chuayboonsong
Publikováno v:
The Journal of Organic Chemistry. 84:13410-13429
In four steps from the tricyclic core, palodesangren B trimethyl ether and palodesangren D dimethyl ether could be synthesized in 29 and 18% overall yields, respectively. A reaction sequence compri...
Autor:
Somsak Ruchirawat, Poonsakdi Ploypradith, Koki Matsumoto, Sirilak Wangngae, Chuthamat Duangkamol, Poramate Songthammawat
Publikováno v:
The Journal of Organic Chemistry. 83:5225-5241
The cyclohexene moiety of the tricyclic 6,7-diaryl-tetrahydro-6 H-benzo[ c]chromene core of palodesangrens could be assembled in a biomimetic and step-economical fashion by the Diels-Alder reaction between the electron-rich ( E)-1,3-butadienylarenes
Autor:
Kassrin, Tangdenpaisal, Poramate, Songthammawat, Kornkamon, Akkarasereenon, Kanokpish, Chuayboonsong, Somsak, Ruchirawat, Poonsakdi, Ploypradith
Publikováno v:
The Journal of organic chemistry. 84(21)
In four steps from the tricyclic core, palodesangren B trimethyl ether and palodesangren D dimethyl ether could be synthesized in 29 and 18% overall yields, respectively. A reaction sequence comprising the regioselective MgCl
Autor:
Poramate, Songthammawat, Sirilak, Wangngae, Koki, Matsumoto, Chuthamat, Duangkamol, Somsak, Ruchirawat, Poonsakdi, Ploypradith
Publikováno v:
The Journal of organic chemistry. 83(9)
The cyclohexene moiety of the tricyclic 6,7-diaryl-tetrahydro-6 H-benzo[ c]chromene core of palodesangrens could be assembled in a biomimetic and step-economical fashion by the Diels-Alder reaction between the electron-rich ( E)-1,3-butadienylarenes
Autor:
Punlop Kuntiyong, Sunisa Akkarasamiyo, Chitlada Hemmara, Poramate Songthammawat, Nuanpan Piboonsrinakara
Publikováno v:
Tetrahedron. 67:8034-8040
A formal synthesis of schulzeines B and C, marine natural products with inhibitory effect against α-glucosidase, has been achieved. The key reactions of the synthesis are N-acyliminium ion cyclization, Sharpless asymmetric dihydroxylation, olefin cr
Autor:
Sunisa Akkarasamiyo, Chitlada Hemmara, Nuanpan Piboonsrinakara, Pijitra Bunrod, Poramate Songthammawat, Boonsong Kongkathip, Punlop Kuntiyong, Duangkamol Namborisut, Artid Buaphan
Publikováno v:
ChemInform. 45