1979
DOI: 10.1021/jo00393a052
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Reactions of some aromatic nitro compounds with alkali metal amides

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1980
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Cited by 9 publications
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“…The molecular weight distribution of the oligomers formed as a function of NCO conversion can be modeled. A projection of the influence of a change in reactivity on X w is shown for one of the monomers in Figure , where the stoichiometric imbalance parameter r (defined as less than 1 in the theoretical treatment of size distribution) was set equal to 0.81 . The effect of the reactivity ratio K is most dramatic at conversion greater than 0.4.…”
Section: Resultsmentioning
confidence: 99%
“…The molecular weight distribution of the oligomers formed as a function of NCO conversion can be modeled. A projection of the influence of a change in reactivity on X w is shown for one of the monomers in Figure , where the stoichiometric imbalance parameter r (defined as less than 1 in the theoretical treatment of size distribution) was set equal to 0.81 . The effect of the reactivity ratio K is most dramatic at conversion greater than 0.4.…”
Section: Resultsmentioning
confidence: 99%
“…ONSH aminations on electron-poor nitroarene derivatives have been studied for decades. , The Beier group recently employed the addition of superstoichiometric lithium anilides to nitro­(hetero)­arenes at deeply cryogenic temperatures (below −100 °C), followed by quenching with potassium permanganate in liquid ammonia (Scheme B) …”
mentioning
confidence: 99%