✦ LIBER ✦

Carbon acids. 8. The trimethylammonio group as a model for assessing the polar effects of electron-withdrawing groups

✍ Scribed by Bordwell, F. G.; Van der Puy, Michael.; Vanier, Noel R.

Book ID: 126283057
Publisher: American Chemical Society
Year: 1976
Tongue: English
Weight: 460 KB
Volume: 41
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo00872a049

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The cyano group as a model for an electr

The cyano group as a model for an electron-withdrawing substituent : Two examples

✍ F. Delbecq 📂 Article 📅 1983 🏛 Elsevier Science 🌐 English ⚖ 334 KB

The cyano group as a model for an electr

The cyano group as a model for an electron-withdrawing substituent: Two examples

✍ F. Delbecq 📂 Article 📅 1983 🏛 Elsevier Science 🌐 English ⚖ 212 KB

A qualitative scale for the electron wit

A qualitative scale for the electron withdrawing effect of substituted phenyl groups and heterocycles

✍ Berthold Hoge; Julia Bader 📂 Article 📅 2007 🏛 Elsevier Science 🌐 English ⚖ 232 KB

The infrared carbonyl group frequency of

The infrared carbonyl group frequency of aliphatic carboxylic acids. A probe for the polar effects of alkyl groups.

✍ John Anthony MacPhee; Jacques-Emile Dubois 📂 Article 📅 1978 🏛 Elsevier Science 🌐 French ⚖ 234 KB

A practical approach for assessing the e

A practical approach for assessing the effect of grouping in hierarchical spatio-temporal models

✍ Francesca Bruno,Daniela Cocchi,Lucia Paci 📂 Article 📅 2012 🏛 Springer-Verlag 🌐 English ⚖ 476 KB

Controlling the regioselectivity of lith

Controlling the regioselectivity of lithiation using kinetic isotope effects: Deuterium as a protecting group for carbon

✍ Jonathan Clayden; Jennifer H. Pink; Neil Westlund; Francis X. Wilson 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 284 KB

By substituting deuterium for hydrogen at positions of high kinetic acidity in amides and earbamates, the usual regiochemical course of their reactions with alkyUithiums (ortholithiation vs. lateral lithiation vs. nucleephilic addition) can be altered or overturned by the kinetic isotope effect, The