{"id":35653,"date":"2025-03-20T17:26:35","date_gmt":"2025-03-20T10:26:35","guid":{"rendered":"https:\/\/1dddev.com\/chemsci\/?post_type=ku-personnel&#038;p=35653"},"modified":"2025-04-28T16:26:30","modified_gmt":"2025-04-28T09:26:30","slug":"paiboon-ngernmeesri","status":"publish","type":"ku-personnel","link":"https:\/\/1dddev.com\/chemsci\/ku-personnel\/paiboon-ngernmeesri\/","title":{"rendered":"\u0e23\u0e28.\u0e14\u0e23. \u0e44\u0e1e\u0e1a\u0e39\u0e25\u0e22\u0e4c \u0e40\u0e07\u0e34\u0e19\u0e21\u0e35\u0e28\u0e23\u0e35"},"content":{"rendered":"\n<h2 class=\"wp-block-heading\">\u0e42\u0e0b\u0e40\u0e0a\u0e35\u0e22\u0e25\u0e21\u0e35\u0e40\u0e14\u0e35\u0e22\/\u0e40\u0e27\u0e47\u0e1a\u0e44\u0e0b\u0e15\u0e4c<\/h2>\n\n\n\n<div class=\"grid grid-cols-1 !mb-16 gap-x-4 gap-y-3 | lg:grid-cols-2 lg:gap-x-7\">\n\t\t\t\t\t<a href=\"https:\/\/scholar.google.com\/citations?hl=th&#038;user=MaBS1yUAAAAJ\" aria-label=\"Google Scholar\" target=\"_blank\" class=\"link__card btn-link rounded-xl flex flex-col justify-between overflow-hidden w-full group border-2 border-black\/30 hover:border-primary\">\n\t\t\t\t\n\t\t\t\t\t<div class=\"grid grid-cols-[1fr_18px] gap-0.5 | xl:gap-3 xl:flex justify-between items-end  relative z-10\">\n\t\t\t\t\t\t<span class=\"text-black text-fs14 | lg:text-fs16\">\n\t\t\t\t\t\t\tGoogle Scholar\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<div class=\"icon external\">\n\t\t\t\t\t\t\t\t\t<svg xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewBox=\"0 0 14 14\" fill=\"none\">\n\t\t\t\t\t\t\t\t\t\t<path fill=\"black\" d=\"M14 1.49998C14 0.947692 13.5523 0.499987 13 0.5L3.99998 0.500212C3.44769 0.500225 2.99999 0.947951 3 1.50024C3.00001 2.05252 3.44774 2.50023 4.00002 2.50021L12 2.50002L12.0002 10.5C12.0002 11.0523 12.448 11.5 13.0002 11.5C13.5525 11.5 14.0002 11.0523 14.0002 10.5L14 1.49998ZM2.39368 13.5211L13.7071 2.20709L12.2929 0.79291L0.979434 12.1069L2.39368 13.5211Z\" \/>\n\t\t\t\t\t\t\t\t\t<\/svg>\n\t\t\t\t\t\t\t\t\t<svg xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewBox=\"0 0 14 14\" fill=\"none\">\n\t\t\t\t\t\t\t\t\t\t<path fill=\"black\" d=\"M14 1.49998C14 0.947692 13.5523 0.499987 13 0.5L3.99998 0.500212C3.44769 0.500225 2.99999 0.947951 3 1.50024C3.00001 2.05252 3.44774 2.50023 4.00002 2.50021L12 2.50002L12.0002 10.5C12.0002 11.0523 12.448 11.5 13.0002 11.5C13.5525 11.5 14.0002 11.0523 14.0002 10.5L14 1.49998ZM2.39368 13.5211L13.7071 2.20709L12.2929 0.79291L0.979434 12.1069L2.39368 13.5211Z\" \/>\n\t\t\t\t\t\t\t\t\t<\/svg>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t<\/a>\n\t\t\t\n\n<\/div>\n\n\n<h2 class=\"wp-block-heading\">\u0e27\u0e38\u0e12\u0e34\u0e01\u0e32\u0e23\u0e28\u0e36\u0e01\u0e29\u0e32<\/h2>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Postdoc (Organic Chemistry), Pennsylvania State University, USA<\/li>\n\n\n\n<li>Ph.D. (Chemistry), Pennsylvania State University, USA<\/li>\n\n\n\n<li>B.S. (Chemistry) (Honors with High Distinction), Indiana University, USA<\/li>\n<\/ul>\n\n\n\n<h2 class=\"wp-block-heading\">\u0e07\u0e32\u0e19\u0e27\u0e34\u0e08\u0e31\u0e22<\/h2>\n\n\n\n<ol class=\"wp-block-list\">\n<li>Total synthesis of natural products and biologically active compounds\n<ul class=\"wp-block-list\">\n<li>Total Synthesis of Anticancer Cladoniamide G<\/li>\n\n\n\n<li>Total Synthesis of Anticancer Melatonine A<\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Invention of novel and useful methodologies for organic systhesis<\/li>\n\n\n\n<li>Investigation of reaction mechanisms<\/li>\n<\/ol>\n\n\n\n<figure class=\"wp-block-image size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"896\" height=\"182\" src=\"http:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/60RFpbn1.png\" alt=\"\" class=\"wp-image-35619\" srcset=\"https:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/60RFpbn1.png 896w, https:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/60RFpbn1-300x61.png 300w, https:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/60RFpbn1-768x156.png 768w\" sizes=\"auto, (max-width: 896px) 100vw, 896px\" \/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"925\" height=\"279\" src=\"http:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/60RFpbn2.png\" alt=\"\" class=\"wp-image-35620\" srcset=\"https:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/60RFpbn2.png 925w, https:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/60RFpbn2-300x90.png 300w, https:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/60RFpbn2-768x232.png 768w\" sizes=\"auto, (max-width: 925px) 100vw, 925px\" \/><\/figure>\n\n\n\n<h2 class=\"wp-block-heading\">\u0e1c\u0e25\u0e07\u0e32\u0e19\u0e27\u0e34\u0e08\u0e31\u0e22<\/h2>\n\n\n\n<p class=\"wp-block-paragraph\">Publications<\/p>\n\n\n\n<ol class=\"wp-block-list\">\n<li>Thanetchaiyakupa, A.; Rattanarata, H.; Areea, S.; Duangthongyou, T.; Nanok, T. Chuanopparata, N.; Ngernmeesri, P. \u201cProtecting-group-free total synthesis of anticancer (\u00b1)-melotenine A\u201d Synthesis 2021. DOI: <a href=\"http:\/\/dx.doi.org\/10.1055\/a-1633-8333\">10.1055\/a-1633-8333<\/a><\/li>\n\n\n\n<li>Thanetchaiyakup, A; Borwornpinyo, S.; Rattanarat, H.; Kanjanasirirat, P.; Jearawuttanakul, K.; Seemakhan, S.; Chuanopparat, N.; Ngernmeesri, P. \u201cCopper-catalyzed synthesis and anticancer activity evaluation of indolo[1,2-a]quinoline derivatives\u201d Tetrahedron Lett. 2021. DOI: 10.1016\/j.tetlet.2021.153365<\/li>\n\n\n\n<li>Taweesak, P.; Thongaram, P.; Kraikruan, P.; Thanetchaiyakup, A.; Chuanopparat, N.; Hsieh, H.-P.; Uang, B.-J.; Ngernmeesri, P. \u201cOne-pot synthesis of dibenzo[b,f]oxepines and total synthesis of bauhinoxepin C\u201d J. Org. Chem. 2021, 86, 1955-1963. DOI: 10.1021\/acs.joc.0c02452<\/li>\n\n\n\n<li>Thongaram, P.; Borwornpinyo, S.; Kanjanasirirat, P.; Jearawuttanakul, K.; Kongsema, M.; Chuanopparat, N.; Ngernmeesri, P. \u201cSynthesis and anticancer activity evaluation of benzo[6,7]oxepino[3,2-b] pyridine derivatives\u201d Tetrahedron 2020, 76, article 131473, 1-11. DOI: 10.1016\/j.tet.2020.131473<\/li>\n\n\n\n<li>Thanetchaiyakup, A.; Rattanarat, H.; Chuanopparat, N.; Ngernmeesri, P. \u201cOne-pot synthesis of substituted indolo[1,2-a]quinolines under transition-metal-free conditions\u201d Tetrahedron Lett. 2018, 59, 1014-1018. DOI: 10.1016\/j.tetlet.2018.01.085<\/li>\n\n\n\n<li>Khamphaya, W., Ngernmeesri, P. 2016. \u201cToward the total synthesis of anti-HIV waltherione C\u201d PACCON Proceedings, Bangkok, Thailand, 2016, 1523-1526.<\/li>\n\n\n\n<li>Thanetchaiyakup, A., Ngernmeesri, P. \u201cThe Synthesis of indolo[1,2-a]quinoline via nucleophilic aromation substitution\u201d The 11th Conference on Science and Technology for Youth Proceedings, Bangkok, Thailand, 2016, 97-103.<\/li>\n\n\n\n<li>Rattanarat, H., Thanetchaiyakup, A., Ngernmeesri, P. 2016. \u201cThe synthesis of indolo[1,2-a]quinoline via Ullmann reaction\u201d The 11th Conference on Science and Technology for Youth Proceedings, Bangkok, Thailand, 2016, 104-111.<\/li>\n\n\n\n<li>Ngernmeesri, P.; Soonkit, S.; Konkhum, A.; Kongkathip, B. \u201cFormal synthesis of (\u00b1)-cladoniamide G\u201d Tetrahedron Lett. 2014, 55, 1621-1624. DOI: 10.1016\/j.tetlet.2014.01.086<\/li>\n\n\n\n<li>Aree, S., and Ngernmeesri, P. \u201cToward the synthesis of anticancer (\u00b1)-melotenine A\u201d PACCON Proceedings, Khon Kaen, Thailand, 2014, 161-163.<\/li>\n\n\n\n<li>Wangchareansak, T.; Sangma, C.; Ngernmeesri, P.; Thitithanyanont, A.; Lieberzeit, P. A. \u201cSelf-assembled glucosamine monolayers as biomimetic receptors for detecting WGA lectin and influenza virus with a quartz crystal microbalance\u201d Anal Bioanal Chem 2013, 405, 6471-6478. DOI: 10.1007\/s00216-013-7057-0<\/li>\n\n\n\n<li>Soonkit, S., Ngernmeesri, P., Kongkathip, B. \u201cToward the synthesis of (\u00b1)-cladoniamide G\u201d PACCON Proceedings, Bangsaen Beach, Thailand, 2013, 820-823.<\/li>\n\n\n\n<li>Feldman, K. S.; Ngernmeesri, P. \u201cTotal synthesis of (\u00b1)-dragmacidin E; problems solved and lessons learned\u201d Synlett. 2012, 23, 1882-1892. DOI: 10.1055\/s-0031-1290692<\/li>\n\n\n\n<li>Feldman, K. S.; Ngernmeesri, P. \u201cTotal synthesis of (\u00b1)-dragmacidin E\u201d Org. Lett. 2011, 13, 5704-5707. DOI: 10.1021\/ol202535f<\/li>\n\n\n\n<li>Feldman, K. S.; Ngernmeesri, P. \u201cDragmacidin E synthesis studies. Preparation of a model heptacyclic core structure\u201d Org. Lett. 2010, 12, 4502-4505. DOI: 10.1021\/ol1018008<\/li>\n\n\n\n<li>Feldman, K. S.; Ngernmeesri, P. \u201cDragmacidin E synthesis studies. Preparation of a model cycloheptannelated indole fragment\u201d Org. Lett. 2005, 7, 5449\u20135452. DOI: 10.1021\/ol0522081<\/li>\n\n\n\n<li>Gajewski, J. J.; Ngernmeesri, P. \u201cEquilibrium constants between boron trifluoride etherate and carbonyl compounds in chloroform solution\u201d Org. Lett. 2000, 2, 2813\u20132815. DOI: 10.1021\/ol000164k<\/li>\n<\/ol>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>\u0e15\u0e33\u0e23\u0e32<\/strong><\/p>\n\n\n\n<ol class=\"wp-block-list\">\n<li>\u0e44\u0e1e\u0e1a\u0e39\u0e25\u0e22\u0e4c \u0e40\u0e07\u0e34\u0e19\u0e21\u0e35\u0e28\u0e23\u0e35. 2563. \u201c\u0e40\u0e04\u0e21\u0e35\u0e2d\u0e34\u0e19\u0e17\u0e23\u0e35\u0e22\u0e4c (01403221)\u201d \u0e01\u0e23\u0e38\u0e07\u0e40\u0e17\u0e1e\u0e21\u0e2b\u0e32\u0e19\u0e04\u0e23: \u0e42\u0e23\u0e07\u0e1e\u0e34\u0e21\u0e1e\u0e4c \u0e2b\u0e49\u0e32\u0e07\u0e2b\u0e38\u0e49\u0e19\u0e2a\u0e48\u0e27\u0e19\u0e08\u0e33\u0e01\u0e31\u0e14 \u0e21\u0e35\u0e19 \u0e40\u0e0b\u0e2d\u0e23\u0e4c\u0e27\u0e34\u0e2a \u0e0b\u0e31\u0e1e\u0e1e\u0e25\u0e32\u0e22. 320 \u0e2b\u0e19\u0e49\u0e32.<\/li>\n<\/ol>\n","protected":false},"featured_media":35622,"parent":0,"template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-35653","ku-personnel","type-ku-personnel","status-publish","has-post-thumbnail","hentry"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.3 - 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