Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Nantamon Supantanapong"'
Autor:
Pavitra Laohapaisan, Kanyapat Lumyong, Jumreang Tummatorn, Charnsak Thongsornkleeb, Jaruwan Chatwichien, Nantamon Supantanapong, Somsak Ruchirawat
Publikováno v:
Chemistry – An Asian Journal. 17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::189a8106f884b0535fda3f6159212600
https://doi.org/10.1002/asia.202101322
https://doi.org/10.1002/asia.202101322
Autor:
Jumreang Tummatorn, Somsak Ruchirawat, Jaruwan Chatwichien, Nantamon Supantanapong, Charnsak Thongsornkleeb, Kanyapat Lumyong, Pavitra Laohapaisan
Publikováno v:
Chemistry – An Asian Journal. 17
ortho-Alkynylarylketone derivatives were employed as key precursors for a one-pot synthesis of arylnaphthalenelactone and furanonaphthol libraries. In this work, we discovered a cost-effective protocol to prepare arylnaphthalenelactones in one-pot us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3299051966e538beb53c54041c3d15a
https://doi.org/10.1002/asia.202101212
https://doi.org/10.1002/asia.202101212
Autor:
Charnsak Thongsornkleeb, Pavitra Laohapaisan, Nantamon Supantanapong, Lukana Ngiwsara, Nisachon Khunnawutmanotham, Warabhorn Rodphon, Jumreang Tummatorn, Kriengsak Lirdprapamongkol, Jisnuson Svasti, Onrapak Reamtong, Somsak Ruchirawat
Publikováno v:
ChemMedChem. 16(24)
Eighteen hybrid compounds between 8-bromo-2-fluoro-isocryptolepine (4) and 1,2,3-triazole were synthesized via azide rearrangement-annulation reaction. Compound 4 underwent regioselective N-propargylation and click reaction to form 8-bromo-2-fluoro-i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c7603100bed710e9390916393b79ec9
https://pubmed.ncbi.nlm.nih.gov/34610210
https://pubmed.ncbi.nlm.nih.gov/34610210
Autor:
Charnsak Thongsornkleeb, Jumreang Tummatorn, Somsak Ruchirawat, Pennapa Chuangsoongnern, Nantamon Supantanapong
Publikováno v:
Organic Chemistry Frontiers. 6:1340-1355
The development of novel methods for the construction of valuable fluorophores, 3-carbonyl-4-arylbenzo[f]indoles and 3-carbonyl-4-arylnaphthofurans, is described. In this protocol, the important polycarbonyl key intermediate was generated via the ket
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a744e802e1b2a33f8a6daa31cb8986c8
https://doi.org/10.1039/c8qo01182f
https://doi.org/10.1039/c8qo01182f
Publikováno v:
Acc Chem Res
Accounts of chemical research, vol 54, iss 5
Accounts of chemical research, vol 54, iss 5
Halogenated natural products number in the thousands, but only in rare cases are the evolutionary advantages conferred by the halogens understood. We set out to investigate the lissoclimide family of cytotoxins, which includes several chlorinated mem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f0994f693c7e15becee6b58fbe8f1f7
https://europepmc.org/articles/PMC8112881/
https://europepmc.org/articles/PMC8112881/
Autor:
Khalil A. Abboud, Nantamon Supantanapong, Helmi-Ulrika Kirm, Minami Odagi, Jaan Saame, Weici Xu, Ivo Leito, Daniel Seidel, Zhengbo Zhu
Publikováno v:
Journal of the American Chemical Society. 142(36)
Readily available 1,2-amino alcohols provide the framework for a new generation of chiral carboxylic acid catalysts that rival the acidity of the widely used chiral phosphoric acid catalyst (S)-TRIP. Covalently linked thiourea sites stabilize the car
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c327fd68df97d7274faaa9832b347d8
https://pubmed.ncbi.nlm.nih.gov/32830974
https://pubmed.ncbi.nlm.nih.gov/32830974
Autor:
Pavitra Laohapaisan, Jumreang Tummatorn, Bhornrawin Akkachairin, Phongprapan Nimnual, Nantamon Supantanapong, Krissada Norseeda, Somsak Ruchirawat, Warabhorn Rodphon, Satapanawat Sittihan, Charnsak Thongsornkleeb, Pennapa Chuangsoongnern
Publikováno v:
Asian Journal of Organic Chemistry. 7:932-945
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6f0b6f4659cea5ad159b07e2fa3ad37
https://doi.org/10.1002/ajoc.201800025
https://doi.org/10.1002/ajoc.201800025
Autor:
Somsak Ruchirawat, Bhornrawin Akkachairin, Nantamon Supantanapong, Phongprapan Nimnual, Charnsak Thongsornkleeb, Jumreang Tummatorn
Publikováno v:
The Journal of Organic Chemistry. 82:3727-3740
ortho-Carbonylarylacetylenols have been employed for the synthesis of dihydronaphthofurans via AgTFA-catalyzed annulation reaction. A broad range of substrates both ortho-keto- and ortho-formylarylacetylenols could be employed in this transformation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e883bb36696dcd1f0e1232ecad8ab03
https://doi.org/10.1021/acs.joc.7b00198
https://doi.org/10.1021/acs.joc.7b00198