{"id":15,"date":"2022-06-04T14:44:38","date_gmt":"2022-06-04T14:44:38","guid":{"rendered":"http:\/\/profstefanberger.de\/?page_id=15"},"modified":"2022-09-29T18:30:45","modified_gmt":"2022-09-29T18:30:45","slug":"publications-1975-1971","status":"publish","type":"page","link":"https:\/\/profstefanberger.de\/?page_id=15","title":{"rendered":"Publications 1975 &#8211; 1971"},"content":{"rendered":"<p><span style=\"font-family: arial, helvetica, sans-serif;\"><\/span><\/p>\r\n<h5 style=\"text-align: center;\"><span style=\"color: #000000;\">No 1 &#8211; 13<\/span><\/h5>\r\n<p><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt; color: #000000;\"><b>Publications 1975<\/b><\/span><\/p>\r\n<ul style=\"list-style-type: circle;\">\r\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">A. Rieker, G. Henes, S. Berger \u201cOxepine III. Ein neuer Syntheseweg ausgehend von 2.5-Cyclohexadien-1.4-diolen\u201d <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>Chem. Ber. <\/i><b>1975<\/b>, <i>108<\/i>, 3700\u20133720.<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1002\/cber.19751081204\">DOI: 10.1002\/cber.19751081204<\/a>.<br \/><br \/><\/span><\/li>\r\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">S. Berger, K. P. Zeller \u201c<sup>13<\/sup>C,<sup>13<\/sup>C Long Range Spin-Spin Coupling Constants in Naphthalene Derivatives\u201d <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>J. C. S. Chem. Comm.<\/i> <b>1975<\/b>, 423\u2013424. <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1039\/C39750000423\">DOI: 10.1039\/C39750000423<\/a>.<br \/><br \/><\/span><\/li>\r\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">E. Breitmaier, K. H. Spohn, S. Berger \u201c<sup>13<\/sup>C Spin-Gitter-Relaxationszeiten und die Beweglichkeit gel\u00f6ster organischer Molek\u00fcle\u201d<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>Angewandte Chemie<\/i> <b>1975<\/b> <i>, 87, <\/i> 152\u2013168, Int. Ed. <b>1975<\/b>, <i>14<\/i>, 144\u2013159. <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1002\/anie.197501441\">DOI: 10.1002\/anie.197501441<\/a>.<br \/><br \/><\/span><\/li>\r\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">S. Berger, F. R. Kreissl, D. M. Grant, J. D. Roberts \u201cDetermination of Anisotropy of Molecular Motion with <sup>13<\/sup>C Spin-Lattice Relaxation Times\u201d <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">J<i>. Am. Chem. Soc.<\/i> <b>1975<\/b>, <i>97<\/i>, 1805\u20131808. <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1021\/ja00840a033\">DOI: 10.1021\/ja00840a033<\/a>.<br \/><br \/><\/span><\/li>\r\n<\/ul>\r\n<p><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt; color: #000000;\"><b>Publications 1974<\/b><\/span><\/p>\r\n<ul style=\"list-style-type: circle;\">\r\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">R. S. Becker. S. Berger, D. K. Dalling, D. M. Grant, R. J. Pugmire \u201cCarbon-13 Magnetic Resonance Investigation of Retinal Isomers and Related Compounds\u201d <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>J. Am. Chem. Soc. <\/i> <b>1974<\/b>, <i>96<\/i><b>,<\/b> 7008\u20137014. <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1021\/ja00829a032\">DOI: 10.1021\/ja00829a032<\/a>.<br \/><br \/><\/span><\/li>\r\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">S. Berger, J. D. Roberts \u201cNuclear Magnetic Resonance Spectroscopy.<sup> 13<\/sup>C,<sup>15<\/sup>N Coupling Constants as a Conformational Probe?\u201d <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>J. Am. Chem. Soc. <\/i><b> 1974<\/b>, <i>96<\/i>, 6757\u20136759. <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1021\/ja00828a036\">DOI: 10.1021\/ja00828a036<\/a>.<br \/><br \/><\/span><\/li>\r\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">S. Berger, F. R. Kreissl, J. D. Roberts \u201cNuclear Magnetic Resonance Spectroscopy. Carbon-13 T<sub>1<\/sub> Measurements of Cycloalkanes\u201d <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>J. Am. Chem. Soc. <\/i><b>1974<\/b> , <i>96<\/i>, 4348. <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1021\/ja00820a063\">DOI: 10.1021\/ja00820a063<\/a>.<br \/><br \/><\/span><\/li>\r\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">S . Berger, A. Rieker \u201cZur <sup>13<\/sup>C-NMR Spektroskopie von Oxepinen\u201d <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>Org. Magn. Res. <\/i><b>1974<\/b>, <i>6<\/i>, 78\u201384. <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1002\/mrc.1270060205\">DOI: 10.1002\/mrc.1270060205<\/a>.<br \/><br \/><\/span><\/li>\r\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">S. Berger, A. Rieker \u201cIdentification and Determination of Quinones\u201d <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">in <i>\u201cThe Chemistry of the Quinonoid Compounds\u201d,<\/i> S. Patai (Hrsg.) <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">Wiley Interscience, New York <b>1974<\/b>, 163\u2013229.<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1002\/9780470771297.ch4\">DOI: 10.1002\/9780470771297.ch4<\/a>.<br \/><br \/><\/span><\/li>\r\n<\/ul>\r\n<p><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt; color: #000000;\"><b>Publications 1972<\/b><\/span><\/p>\r\n<ul style=\"list-style-type: circle;\">\r\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">A. Rieker, S. Berger \u201c<sup>13<\/sup>CMR-Untersuchungen an Cyclohexadienonen\u201d <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>Org. Magn. Res. <\/i><b>1972<\/b>, <i>4<\/i>, 857\u2013873. <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1002\/mrc.1270040610\">DOI: 10.1002\/mrc.1270040610<\/a>.<br \/><br \/><\/span><\/li>\r\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">S. Berger, S. Hauff, P. Niederer, A. Rieker \u201c<sup>13<\/sup>C-Polarization Observed During Reduction of Diazonium Salts Using the Pulse Fourier Transform Technique\u201d <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>Tetrahedron Letters <\/i> <b>1972<\/b>, <i>13<\/i>, 2581\u20132584.<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1016\/S0040-4039(01)84879\u20136\">DOI: 10.1016\/S0040-4039(01)84879\u20136<\/a>.<br \/><br \/><\/span><\/li>\r\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">S. Berger, A. Rieker \u201c<sup>13<\/sup>C-Fourier-Transform-Spektroskopie von ortho- und para-Benzochinonen. Korrelation zwischen chemischer Verschiebung und anderen Molek\u00fcldaten\u201d <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>Tetrahedron <\/i><b>1972<\/b>,<i> 28<\/i>, 3123\u20133139. <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1016\/0040-4020(72)80026-7\">DOI: 10.1016\/0040-4020(72)80026-7<\/a>.<br \/><br \/><\/span><\/li>\r\n<\/ul>\r\n<p><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt; color: #000000;\"><b>Publications 1971<\/b><\/span><\/p>\r\n<ul style=\"list-style-type: circle;\">\r\n<li style=\"margin-bottom: 0px;\"><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\">S. Berger, G. Henes, A. Rieker \u201cOxepine durch Dehydratisierung von 1.4-Dihydroxy-Cyclohexadienen\u201d<\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><i>Tetrahedron Letters <\/i><b>1971<\/b>, <i>12<\/i>, 1257\u20131260. <\/span><br \/><span style=\"font-family: arial, helvetica, sans-serif; font-size: 14pt;\"><a href=\"https:\/\/www.doi.org\/10.1016\/S0040\u20134039(01)96680\u20138\">DOI: 10.1016\/S0040\u20134039(01)96680\u20138<\/a>.<\/span><\/li>\r\n<\/ul>\r\n","protected":false},"excerpt":{"rendered":"<p>No 1 &#8211; 13 Publications 1975 A. Rieker, G. Henes, S. Berger \u201cOxepine III. Ein neuer Syntheseweg ausgehend von 2.5-Cyclohexadien-1.4-diolen\u201d Chem. Ber. 1975, 108, 3700\u20133720.DOI: 10.1002\/cber.19751081204. S. Berger, K. P. Zeller \u201c13C,13C Long Range Spin-Spin Coupling Constants in Naphthalene Derivatives\u201d J. C. S. Chem. Comm. 1975, 423\u2013424. DOI: 10.1039\/C39750000423. E. Breitmaier, K. H. Spohn, S. [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":10,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-15","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/profstefanberger.de\/index.php?rest_route=\/wp\/v2\/pages\/15","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/profstefanberger.de\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/profstefanberger.de\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/profstefanberger.de\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/profstefanberger.de\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=15"}],"version-history":[{"count":45,"href":"https:\/\/profstefanberger.de\/index.php?rest_route=\/wp\/v2\/pages\/15\/revisions"}],"predecessor-version":[{"id":661,"href":"https:\/\/profstefanberger.de\/index.php?rest_route=\/wp\/v2\/pages\/15\/revisions\/661"}],"up":[{"embeddable":true,"href":"https:\/\/profstefanberger.de\/index.php?rest_route=\/wp\/v2\/pages\/10"}],"wp:attachment":[{"href":"https:\/\/profstefanberger.de\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=15"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}