Reactions of N-substituted pyridinium cations with carbanions: 5,6,8,9-tetrahydro-7-phenylbisbenzo[ah]acridine, a superior leaving group
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1981/P1/P19810000661
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2. Reactivity of aryl- and heteroarylmalonates againstortho-dinucleophiles. Triaryl(heteroaryl)methane synthesis;Journal of Heterocyclic Chemistry;1987-01
3. Kinetics and mechanism of nucleophilic displacements with heterocycles as leaving groups. Part 23. Studies at the borderlines between reactions proceeding (i) via free carbocations, (ii) via rate-determining formation of ion–molecule pairs, and (iii) via rate-determining nucleophilic attack on ion–molecule pairs;Canadian Journal of Chemistry;1986-06-01
4. Nucleophilic displacement with heterocycles as leaving groups. Part 16. Reactions of secondary alkyl primary amines with 5,6,8,9-tetrahydro-7-phenyldibenzo[c,h]xanthylium trifluoromethanesulphonate to give intermediates solvolysing without rearrangement;Journal of the Chemical Society, Perkin Transactions 2;1985
5. Replacement of primary amino groups by hydrogen via tetrahydrodibenzacridinium salts;Journal of the Chemical Society, Perkin Transactions 1;1984
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