{"id":35662,"date":"2025-03-20T17:57:30","date_gmt":"2025-03-20T10:57:30","guid":{"rendered":"https:\/\/1dddev.com\/chemsci\/?post_type=ku-personnel&#038;p=35662"},"modified":"2025-04-28T15:53:19","modified_gmt":"2025-04-28T08:53:19","slug":"sunisa-akkarasamiyo","status":"publish","type":"ku-personnel","link":"https:\/\/1dddev.com\/chemsci\/ku-personnel\/sunisa-akkarasamiyo\/","title":{"rendered":"\u0e1c\u0e28. \u0e14\u0e23. \u0e2a\u0e38\u0e19\u0e34\u0e2a\u0e32 \u0e2d\u0e31\u0e04\u0e04\u0e30\u0e23\u0e31\u0e2a\u0e21\u0e34\u0e42\u0e22"},"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=rKEAvOYAAAAJ\" 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) Stockholm University, Sweden<\/li>\n\n\n\n<li>Postdoc (Organic chemistry) Uppsala University, Sweden<\/li>\n\n\n\n<li>Ph.D. (Chemistry), Kasetsart University, Bangkok, Thailand<\/li>\n\n\n\n<li>M.Sc. (Organic Chemistry), Silpakorrn University, Nakhon Pathom, Thailand<\/li>\n\n\n\n<li>B.Sc. (Chemistry) Silpakorrn University, Nakhon Pathom, Thailand<\/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<p class=\"wp-block-paragraph\">Our research works focus on development of synthetic methodology and synthesis of biologically active compounds based on green chemistry concept.<\/p>\n\n\n\n<ol class=\"wp-block-list\">\n<li><strong>C-O bond cleavage of alcohols and ethers<\/strong>\n<ul class=\"wp-block-list\">\n<li><strong>Deoxygenation of epoxides to alkenes<\/strong><br>This methodology could be an alternative approach for alkene isomerization and also one of the method for utilization of biomass as renewable chemicals.<\/li>\n\n\n\n<li><strong>Suzuki-Miyaura cross-coupling of benzylic alcohols<\/strong><br>C(sp<sup>3<\/sup>)-C(sp<sup>2<\/sup>) bond formation via Suzuki-Miyaura cross-coupling of non-derivatized benzylic alcohols is a greener alternative method to use benzylic halides is ongoing to develop.<\/li>\n<\/ul>\n<\/li>\n\n\n\n<li><strong>2. Asymmetric synthesis of biologically active molecules<\/strong>\n<ul class=\"wp-block-list\">\n<li><strong>2.1 Synthesis of Chrysosporazine A-C<\/strong><\/li>\n<\/ul>\n<\/li>\n<\/ol>\n\n\n\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"515\" src=\"http:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/sunisa-1-1024x515.jpg\" alt=\"\" class=\"wp-image-35634\" srcset=\"https:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/sunisa-1-1024x515.jpg 1024w, https:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/sunisa-1-300x151.jpg 300w, https:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/sunisa-1-768x386.jpg 768w, https:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/sunisa-1.jpg 1151w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"248\" src=\"http:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/sunisa-2-1024x248.jpg\" alt=\"\" class=\"wp-image-35635\" srcset=\"https:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/sunisa-2-1024x248.jpg 1024w, https:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/sunisa-2-300x73.jpg 300w, https:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/sunisa-2-768x186.jpg 768w, https:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/sunisa-2.jpg 1155w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/figure>\n\n\n\n<figure class=\"wp-block-image\"><img decoding=\"async\" src=\"https:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/sunisa-2.jpg\" alt=\"\"\/><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\">References : <em>Org. Lett.<\/em> <strong>2019<\/strong>, <em>21<\/em>, 4782-4787, Synthesis <strong>2020<\/strong>, <em>52<\/em>, 645-659.<\/p>\n\n\n\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"322\" src=\"http:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/sunisa-3-1024x322.jpg\" alt=\"\" class=\"wp-image-35636\" srcset=\"https:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/sunisa-3-1024x322.jpg 1024w, https:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/sunisa-3-300x94.jpg 300w, https:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/sunisa-3-768x242.jpg 768w, https:\/\/1dddev.com\/chemsci\/wp-content\/uploads\/2025\/03\/sunisa-3.jpg 1240w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/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<ul class=\"wp-block-list\">\n<li><strong>Akkarasamiyo, S<\/strong>.; Rujirawat, S.; Ploypradith, P.; Samec, J.S.M. Transition-Metals Catalyzed Suzuki-Miyaura Type Cross Coupling Reaction of p-Activated Alcohols <em>Synthesis <\/em><strong>2020<\/strong><em>, 52(5)<\/em>, 645-659<\/li>\n\n\n\n<li><strong>Akkarasamiyo, S<\/strong>.; Samec, J.S.M. Intermolecular Stereospecific Substitution of Underivatized Enantioenriched Secondary Alcohols by Organocatalysis (Highlight) <em>Angew. Chem. Int. Ed.<\/em> <strong>2019<\/strong>, <em>58<\/em>(50), 17908-17910.<\/li>\n\n\n\n<li>Watile, R. A.; Bunrit, A.; Margalef, J.; <strong>Akkarasamiyo, S<\/strong>.; Ayub, R.; Lagerspets, E.; Biswas, S.; Repo, T.; Samec, J.S.M. Intramolecular substitutions of secondary and tertiary alcohols with chirality transfer by an iron (III) catalyst <em>Nature Comm<\/em>. <strong>2019<\/strong>, 10:3826.<\/li>\n\n\n\n<li><strong>Akkarasamiyo, S<\/strong>.; Margalef, J.; Samec, J. S. M. Nickel-Catalyzed Suzuki-Miyaura Cross-Coupling Reaction of Naphthyl and Quinolyl Alcohols with Boronic Acids <em>Org. Lett<\/em>. <strong>2019<\/strong>, 21, 4782-4787.<\/li>\n\n\n\n<li>Rukkijakan, T.; <strong>Akkarasamiyo, S<\/strong>.; Sawadjoon, S.; Samec, J. S. M. Pd-catalyzed substitution of the OH group of non-derivatized allylic alcohols by phenols <em>J. Org. Chem. <\/em><strong>2018<\/strong><em>, <\/em>83(7), 4099-4104.<\/li>\n\n\n\n<li><strong>Akkarasamiyo, S.;<\/strong> Sawadjoon, S.; Orthaber, A.; Samec, J. S. M. Tsuji-Trost Reaction of Non-Derivatized Allylic Alcohols. <em>Chem. Eur. J.<\/em>&nbsp; <strong>2018<\/strong>, 24(14), 3488\u20133498.<\/li>\n\n\n\n<li>Gupta, A. K.; <strong>Akkarasamiyo, S.<\/strong>; Orthaber, A. Rich Coordination Chemistry of \u03c0\u2011Acceptor Dibenzoarsole Ligands. <em>Inorg. Chem<\/em>. <strong>2017<\/strong>, 56, 4504\u22124511.<\/li>\n<\/ul>\n","protected":false},"featured_media":35637,"parent":0,"template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-35662","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 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>\u0e1c\u0e28. \u0e14\u0e23. \u0e2a\u0e38\u0e19\u0e34\u0e2a\u0e32 \u0e2d\u0e31\u0e04\u0e04\u0e30\u0e23\u0e31\u0e2a\u0e21\u0e34\u0e42\u0e22 - \u0e20\u0e32\u0e04\u0e27\u0e34\u0e0a\u0e32\u0e40\u0e04\u0e21\u0e35 \u0e04\u0e13\u0e30\u0e27\u0e34\u0e17\u0e22\u0e32\u0e28\u0e32\u0e2a\u0e15\u0e23\u0e4c \u0e21\u0e2b\u0e32\u0e27\u0e34\u0e17\u0e22\u0e32\u0e25\u0e31\u0e22\u0e40\u0e01\u0e29\u0e15\u0e23\u0e28\u0e32\u0e2a\u0e15\u0e23\u0e4c<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/1dddev.com\/chemsci\/ku-personnel\/sunisa-akkarasamiyo\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"\u0e1c\u0e28. \u0e14\u0e23. \u0e2a\u0e38\u0e19\u0e34\u0e2a\u0e32 \u0e2d\u0e31\u0e04\u0e04\u0e30\u0e23\u0e31\u0e2a\u0e21\u0e34\u0e42\u0e22 - \u0e20\u0e32\u0e04\u0e27\u0e34\u0e0a\u0e32\u0e40\u0e04\u0e21\u0e35 \u0e04\u0e13\u0e30\u0e27\u0e34\u0e17\u0e22\u0e32\u0e28\u0e32\u0e2a\u0e15\u0e23\u0e4c \u0e21\u0e2b\u0e32\u0e27\u0e34\u0e17\u0e22\u0e32\u0e25\u0e31\u0e22\u0e40\u0e01\u0e29\u0e15\u0e23\u0e28\u0e32\u0e2a\u0e15\u0e23\u0e4c\" \/>\n<meta property=\"og:description\" content=\"\u0e42\u0e0b\u0e40\u0e0a\u0e35\u0e22\u0e25\u0e21\u0e35\u0e40\u0e14\u0e35\u0e22\/\u0e40\u0e27\u0e47\u0e1a\u0e44\u0e0b\u0e15\u0e4c \u0e27\u0e38\u0e12\u0e34\u0e01\u0e32\u0e23\u0e28\u0e36\u0e01\u0e29\u0e32 \u0e07\u0e32\u0e19\u0e27\u0e34\u0e08\u0e31\u0e22 Our research works focus on development of synthetic methodology and synthesis of biologically active compounds based on green chemistry concept. References : Org. 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