𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Hydrolysis of the methyl 2-methylcyclohexanecarboxylates; conformational analysis of some cyclohexanecarboxylic derivatives

✍ Scribed by Lars H. Hellberg; Robert Peiffer; Thomas L. Jacobs; Russell Reed


Book ID
104215442
Publisher
Elsevier Science
Year
1968
Tongue
French
Weight
313 KB
Volume
9
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


It has been reported (2) that cis-2-methyl-1-acetylcyclohexane [a] exists largely (at least -89%) in the conformation Is (rather than 58% II+ 42% Ia, approximately, assuming additivity of A-values (2,3) and ignoring other considerations), and [b] it reacts faster (33:l) towards hydroxylamine than its isomer (IIIa, neglecting the diaxial conformation). Considerations


📜 SIMILAR VOLUMES


Conformational analysis of oligomeric fl
✍ Jan P. Steynberg; E. Vincent Brandt; Daneel Ferreira; Carin A. Helfer; Wayne L. 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 853 KB

## Abstract The profisetinidins are the most important polyflavanoids of commerce, making up the major constituents of wattle and quebracho tannins. Even within the dimeric profisetinidins, substantial complexity exists because of stereo‐, regio‐, rotational and conformational isomers. Definition o

100 MHz n.m.r. spectra and conformationa
✍ Knut Bergesen; Michael J. Cook; Teh Kim Hock 📂 Article 📅 1976 🏛 John Wiley and Sons 🌐 English ⚖ 505 KB

## Abstract The 100 MHz spectra of 2‐methyl‐, 4‐methyl‐, 4,5,8‐trimethyl‐ and 4,5,7‐trimethyl‐1‐tetralones have been analysed as 8‐spin systems using iterative computation. The monomethyl derivatives exist in inverting half‐chair conformations, the 2‐methyl group favouring the equatorial site and t