Author:
Ansell Herbert V.,Taylor Roger
Publisher
Royal Society of Chemistry (RSC)
Cited by
17 articles.
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1. The quantitative electrophilic reactivity of annulenes. Part 5. Trithiadiazepine, its 6-bromo- and 6-nitro-derivatives, and trithiatriazepine;Journal of the Chemical Society, Perkin Transactions 2;1989
2. Electrophilic aromatic substitution. Part 36. Protiodetritiation of some annelated meta-cyclophanes: effect of ring-buckling on reactivity, and the first example of electrophilic substitution through a hole;Journal of the Chemical Society, Perkin Transactions 2;1987
3. The quantitative electrophilic reactivity of annulenes. Part 2. Partial rate factors for hydrogen exchange of azulene, cycl[3,2,2]azine, indolizine, N-methylisoindole, indole, and pyrrolo[2,1-b]thiazole, and attempted exchange in trans-9,10-dimethyldihydropyrene: the dramatic effect of creating aromaticity in the transition state for electrophilic substitution, and the importance of valence bond theory;Journal of the Chemical Society, Perkin Transactions 2;1987
4. Electrophilic aromatic substitution. Part 35. Deviations from additivity of methyl substituent effects in detritiation of dimethylnaphthalenes: the effect of electron supply on bond fixation;Journal of the Chemical Society, Perkin Transactions 2;1983
5. Electrophilic aromatic substitution. Part 32. Partial rate factors for detritiation of dithieno[2,3-b:3′,2′-d]thiophen, dithieno[3,2-b:2′,3′-d]-thiophen, and dithieno[2,3-b:2′,3′-d]thiophen;J. Chem. Soc., Perkin Trans. 2;1982