{"id":1502,"date":"1995-03-01T13:52:24","date_gmt":"1995-03-01T12:52:24","guid":{"rendered":"http:\/\/www.fluoritech.it\/?p=1502"},"modified":"2025-03-27T17:32:40","modified_gmt":"2025-03-27T16:32:40","slug":"1502","status":"publish","type":"post","link":"https:\/\/www.fluoritech.com\/?p=1502","title":{"rendered":"A new approach to the synthesis of 2,2-difluoro-1,3-dioxolanes"},"content":{"rendered":"<p><!--:en--><!-- [if gte mso 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W;BRAGANTE, L;FONTANA, S;TORTELLI, V; ZEDDA, A.<\/p>\n<p>Source:JOURNAL OF FLUORINE CHEMISTRY<\/p>\n<p>Volume: 71 Issue: 1 Pages: 111-117<\/p>\n<p>DOI: 10.1016\/0022-1139(94)03167-X Published: MAR 1995<\/p>\n<p>ABSTRACT:<\/p>\n<p style=\"text-align: justify;\">A direct and versatile way to prepare halogenated 2,2-difluoro-1,3-dioxolanes through the addition of bis-(fluoroxy)difluoromethane (BDM) to halogenated alkenes (CF2=CFCF3, CF2=CFOCF2CF3, CF2=CHCF3, CF3CF=CFCF3, CFCl=CFCl, CFBr=CFBr, CCl2=CCl2, CHCl=CCl2, CHCl=CHCl, CH2=CHCl, CF2=CFCl, (CF3)(2)CFCF=CFCF3, CF2=CFBr, CF2=CF2) has been discovered.<\/p>\n<p style=\"text-align: justify;\">http:\/\/www.sciencedirect.com\/science\/article\/pii\/002211399403167X<\/p>\n<p><!--:--><!--:it--><\/p>\n<p class=\"MsoNormal\" style=\"margin-bottom: .0001pt; line-height: normal;\"><a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/002211399403167X\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter\" title=\"S00221139\" src=\"http:\/\/www.fluoritech.it\/wp-content\/uploads\/1995\/03\/S00221139.gif\" alt=\"\" width=\"112\" height=\"150\" \/><\/a><\/p>\n<p class=\"MsoNormal\" style=\"margin-bottom: .0001pt; line-height: normal;\"><span style=\"font-size: 12.0pt; font-family: 'Times New Roman','serif'; mso-fareast-font-family: 'Times New Roman'; mso-fareast-language: IT;\">Author(s):NAVARRINI, W;BRAGANTE, L;FONTANA, S;TORTELLI, V; ZEDDA, A. <\/span><\/p>\n<p class=\"MsoNormal\" style=\"margin-bottom: .0001pt; line-height: normal;\"><span lang=\"EN-US\" style=\"font-size: 12.0pt; font-family: 'Times New Roman','serif'; mso-fareast-font-family: 'Times New Roman'; mso-ansi-language: EN-US; mso-fareast-language: IT;\">Source:JOURNAL OF FLUORINE CHEMISTRY <\/span><\/p>\n<p class=\"MsoNormal\" style=\"margin-bottom: .0001pt; line-height: normal;\"><span lang=\"EN-US\" style=\"font-size: 12.0pt; font-family: 'Times New Roman','serif'; mso-fareast-font-family: 'Times New Roman'; mso-ansi-language: EN-US; mso-fareast-language: IT;\">Volume: 71 Issue: 1 <\/span><span lang=\"EN-US\" style=\"font-size: 12.0pt; font-family: 'Times New Roman','serif'; mso-fareast-font-family: 'Times New Roman'; mso-ansi-language: EN-US; mso-fareast-language: IT;\">Pages: 111-117 <\/span><\/p>\n<p class=\"MsoNormal\" style=\"margin-bottom: .0001pt; line-height: normal;\"><span lang=\"EN-US\" style=\"font-size: 12.0pt; font-family: 'Times New Roman','serif'; mso-fareast-font-family: 'Times New Roman'; mso-ansi-language: EN-US; mso-fareast-language: IT;\">DOI: 10.1016\/0022-1139(94)03167-X Published: MAR 1995<\/span><\/p>\n<p><span class=\"FR_label\">ABSTRACT:<\/span><\/p>\n<p style=\"text-align: justify;\">A direct and versatile way to prepare halogenated 2,2-difluoro-1,3-dioxolanes through the addition of bis-(fluoroxy)difluoromethane (BDM) to halogenated alkenes (CF2=CFCF3, CF2=CFOCF2CF3, CF2=CHCF3, CF3CF=CFCF3, CFCl=CFCl, CFBr=CFBr, CCl2=CCl2, CHCl=CCl2, CHCl=CHCl, CH2=CHCl, CF2=CFCl, (CF3)(2)CFCF=CFCF3, CF2=CFBr, CF2=CF2) has been discovered.<\/p>\n<p>http:\/\/www.sciencedirect.com\/science\/article\/pii\/002211399403167X<\/p>\n<p><!--:--><\/p>\n","protected":false},"excerpt":{"rendered":"<p>&nbsp; &nbsp; Author(s):NAVARRINI, W;BRAGANTE, L;FONTANA, S;TORTELLI, V; ZEDDA, A. Source:JOURNAL OF FLUORINE CHEMISTRY Volume: 71 Issue: 1 Pages: 111-117 DOI: 10.1016\/0022-1139(94)03167-X Published: MAR 1995 ABSTRACT: A direct and versatile way to prepare halogenated 2,2-difluoro-1,3-dioxolanes through the addition of bis-(fluoroxy)difluoromethane (BDM) to halogenated alkenes (CF2=CFCF3, CF2=CFOCF2CF3, CF2=CHCF3, CF3CF=CFCF3, CFCl=CFCl, CFBr=CFBr, CCl2=CCl2, CHCl=CCl2, CHCl=CHCl, CH2=CHCl, CF2=CFCl, (CF3)(2)CFCF=CFCF3, [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"saved_in_kubio":false,"footnotes":""},"categories":[15],"tags":[],"class_list":["post-1502","post","type-post","status-publish","format-standard","hentry","category-papers-1995"],"_links":{"self":[{"href":"https:\/\/www.fluoritech.com\/index.php?rest_route=\/wp\/v2\/posts\/1502","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.fluoritech.com\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.fluoritech.com\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.fluoritech.com\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.fluoritech.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=1502"}],"version-history":[{"count":24,"href":"https:\/\/www.fluoritech.com\/index.php?rest_route=\/wp\/v2\/posts\/1502\/revisions"}],"predecessor-version":[{"id":3901,"href":"https:\/\/www.fluoritech.com\/index.php?rest_route=\/wp\/v2\/posts\/1502\/revisions\/3901"}],"wp:attachment":[{"href":"https:\/\/www.fluoritech.com\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=1502"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.fluoritech.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=1502"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.fluoritech.com\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=1502"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}