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Effect of a homoallylic double bond on the rates of solvolysis of 1-phenylcyclopentyl and 2-phenyl-2-norbornanyl p-nitrobenzoates. Evidence for the absence of .pi.-participation as a factor in the high exo:endo rate ratio in the 2-phenyl-2-norbornenyl system

✍ Scribed by Peters, Edward N.; Brown, Herbert C.

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

High exo: endo rate ratio and predominan

✍ Peters, Edward N.; Brown, Herbert C. 📂 Article 📅 1972 🏛 American Chemical Society 🌐 English ⚖ 226 KB

High exo:endo rate ratios in the solvoly

✍ Brown, Herbert Charles; Vander Jagt, David L.; Schleyer, Paul V. R.; Fort, Raymo 📂 Article 📅 1969 🏛 American Chemical Society 🌐 English ⚖ 356 KB

Unusually low exo-endo rate ratio in the

✍ Brown, Herbert Charles.; Ikegami, Shiro. 📂 Article 📅 1968 🏛 American Chemical Society 🌐 English ⚖ 356 KB

Unusually high exo:endo rate ratios in t

✍ Brown, Herbert C.; Takeuchi, Kenichi. 📂 Article 📅 1968 🏛 American Chemical Society 🌐 English ⚖ 338 KB

Structural effects in solvolytic reactio

✍ Brown, Herbert C.; Ikegami, Shiro; Liu, Kwang-Ting; Tritle, Gary L. 📂 Article 📅 1976 🏛 American Chemical Society 🌐 English ⚖ 662 KB

Solvolysis of the 2-aryl-5-methyl-2-norb

✍ Brown, Herbert C.; Ravindranathan, M.; Peters, Edward N. 📂 Article 📅 1974 🏛 American Chemical Society 🌐 English ⚖ 262 KB