{"id":577,"date":"2020-10-27T09:41:48","date_gmt":"2020-10-27T08:41:48","guid":{"rendered":"https:\/\/sites.unimi.it\/apisgroup\/?p=577"},"modified":"2022-01-21T12:58:28","modified_gmt":"2022-01-21T11:58:28","slug":"non-natural-3%e2%80%91arylmorpholino-%ce%b2-amino-acid-as-a-ppii-helix-inducer","status":"publish","type":"post","link":"https:\/\/sites.unimi.it\/apisgroup\/2020\/10\/27\/non-natural-3%e2%80%91arylmorpholino-%ce%b2-amino-acid-as-a-ppii-helix-inducer\/","title":{"rendered":"Non-natural 3\u2011Arylmorpholino-\u03b2-amino Acid as a PPII Helix Inducer"},"content":{"rendered":"\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"421\" height=\"288\" src=\"https:\/\/sites.unimi.it\/apisgroup\/wp-content\/uploads\/2020\/10\/Tocmets7.png\" alt=\"\" class=\"wp-image-578\" srcset=\"https:\/\/sites.unimi.it\/apisgroup\/wp-content\/uploads\/2020\/10\/Tocmets7.png 421w, https:\/\/sites.unimi.it\/apisgroup\/wp-content\/uploads\/2020\/10\/Tocmets7-300x205.png 300w\" sizes=\"auto, (max-width: 421px) 100vw, 421px\" \/><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\">A new non-natural \u03b2-amino acid, named 3-Ar-\u03b2-Morph, was designed and synthesized via a regio- and diastereoselective Pdcatalyzed C(sp3)H-arylation of the corresponding 2S,6S-(6-methoxymorpholin-2-yl)carboxylic acid, readily available from glucose. According to the computational prevision and confirmed by IR and NMR data, the insertion of 3-Ar-\u03b2-Morph in a model foldamer represents a way to stabilize a PPII-like helix through the presence of two \u03b3-turns, secondary structure motifs induced by the morpholine ring, and the trans-tertiary amide bond.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.0c02331\">https:\/\/doi.org\/10.1021\/acs.orglett.0c02331<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>A new non-natural \u03b2-amino acid, named 3-Ar-\u03b2-Morph, was designed and synthesized via a regio- and diastereoselective Pdcatalyzed C(sp3)H-arylation of the corresponding 2S,6S-(6-methoxymorpholin-2-yl)carboxylic acid, readily available from glucose. According to the computational prevision and confirmed&#46;&#46;&#46;<\/p>\n","protected":false},"author":1,"featured_media":578,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[6,5,7],"tags":[32],"class_list":["post-577","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-application","category-peptidomimetics","category-amino-acid","tag-morpholino-beta-amino-acid"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Non-natural 3\u2011Arylmorpholino-\u03b2-amino Acid as a PPII Helix Inducer - APIS group<\/title>\n<meta name=\"description\" content=\"A new non-natural \u03b2-amino acid, named 3-Ar-\u03b2-Morph, was designed and synthesized via a regio- and diastereoselective Pdcatalyzed C(sp3)H-arylation of the corresponding 2S,6S-(6-methoxymorpholin-2-yl)carboxylic acid\" \/>\n<meta name=\"robots\" content=\"noindex, follow\" \/>\n<meta property=\"og:locale\" content=\"it_IT\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Non-natural 3\u2011Arylmorpholino-\u03b2-amino Acid as a PPII Helix Inducer - APIS group\" \/>\n<meta property=\"og:description\" content=\"A new non-natural \u03b2-amino acid, named 3-Ar-\u03b2-Morph, was designed and synthesized via a regio- and diastereoselective Pdcatalyzed C(sp3)H-arylation of the corresponding 2S,6S-(6-methoxymorpholin-2-yl)carboxylic acid\" \/>\n<meta property=\"og:url\" content=\"https:\/\/sites.unimi.it\/apisgroup\/2020\/10\/27\/non-natural-3\u2011arylmorpholino-\u03b2-amino-acid-as-a-ppii-helix-inducer\/\" \/>\n<meta property=\"og:site_name\" content=\"APIS group\" \/>\n<meta property=\"article:published_time\" content=\"2020-10-27T08:41:48+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2022-01-21T11:58:28+00:00\" \/>\n<meta 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