Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Letter
  • Published:

Multiplanar Cyclohexane Rings

Abstract

WITH reference to the letter of Dr. Qudrat-i-Khuda in NATURE of August 24, we wish to state that in this laboratory, the synthesis of the 1-carboxy-4-methyl-cyclohexane-1-acetic acids from the dicyano ester prepared from 4-methylcyclohexanone by Higson and Thorpe's method, led only to a pair of isomerides melting at 137° and 173° respectively. These acids proved identical with the acids previously obtained by oxidation of the isomeric-keto-4-methylcyclo-hexane-l:l-diacetic acids with hydrogen peroxide.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Similar content being viewed by others

References

  1. J. Indian Chem. Soc., 8, 277; 1931.

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

DESAI, R., HUNTER, R. Multiplanar Cyclohexane Rings. Nature 136, 608–609 (1935). https://doi.org/10.1038/136608b0

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/136608b0

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing