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Unusually low exo-endo rate ratio in the solvolysis of the 2,7,7-trimethyl-2-norbornyl p-nitrobenzoates. Evidence for steric effects as a major factor in the exo-endo rate and product ratios of norbornyl derivatives

✍ Scribed by Brown, Herbert Charles.; Ikegami, Shiro.

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

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; Vander Jagt, David L. 📂 Article 📅 1985 🏛 American Chemical Society 🌐 English ⚖ 817 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

Predominant exo substitution in the prod

✍ Takeuchi, Kenichi.; Brown, Herbert C. 📂 Article 📅 1968 🏛 American Chemical Society 🌐 English ⚖ 327 KB

High exo-endo rate ratio and predominate

✍ Brown, Herbert C.; Takeuchi, Kenichi. 📂 Article 📅 1968 🏛 American Chemical Society 🌐 English ⚖ 369 KB

Structural effects in solvolytic reactio

✍ Brown, Herbert C.; Rao, C. Gundu 📂 Article 📅 1979 🏛 American Chemical Society 🌐 English ⚖ 426 KB