1970
DOI: 10.1002/9780470771235.ch4
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Rearrangement and elimination of the amido group

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Cited by 7 publications
(6 citation statements)
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“…[35][36][37] These nitrogen containing compounds can react with carboxylic acids to form amines, 38 (Scheme 1, reaction 1C) which can pyrolyze further to form nitriles. 39 (Scheme 1, reaction 2B).…”
Section: Reaction Pathwaysmentioning
confidence: 99%
“…[35][36][37] These nitrogen containing compounds can react with carboxylic acids to form amines, 38 (Scheme 1, reaction 1C) which can pyrolyze further to form nitriles. 39 (Scheme 1, reaction 2B).…”
Section: Reaction Pathwaysmentioning
confidence: 99%
“…Systematic studies focusing on the dependence of FLP-reactivity on the p K a of the conjugate Brønsted acid ,, support that chloride should be able to activate H 2 (p K a (MeCN): 10.30) provided that it does not deactivate the Lewis acid ( vide supra) . We were able to exclude the amide and the chloroimine, which may arise from nucleophilic ring opening as active Lewis bases in the H 2 splitting (see SI). Instead we observed the fast isotope scrambling of a H 2 /D 2 mixture by 3 in the presence of the chloride sources 8 , 9 , and 10 at 50−70 °C (Scheme ).…”
mentioning
confidence: 99%
“…50 However, cross-border flow of information, as its name indicates, has a transnational nature. 51 In the international trade context, it advocates for Internet Service Providers ("ISPs") to have non-discriminated access to a foreign market.…”
Section: Weak Protection Of Cross-border Flow Of Informationmentioning
confidence: 99%