Issue 2, 1972

Shielding effects of the diphenylmethanol substituent in certain anisole derivatives: a method for determination of the site of metallation

Abstract

A potentially valuable tool for isomer identification of lithio-aromatics consists of condensation of the lithio-intermediate with benzophenone and examination of the effect on the chemical shift of various alkyl substituent protons in the molecule: alkyl protons adjacent to the diphenylmethanol substituent invariably experience a significant upfield shift.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 54-55

Shielding effects of the diphenylmethanol substituent in certain anisole derivatives: a method for determination of the site of metallation

D. W. Slocum and C. A. Jennings, J. Chem. Soc., Chem. Commun., 1972, 54 DOI: 10.1039/C39720000054

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements