Highly chemoselective synthesis of 1,2,3,4,5-pentasubstituted cyclohexanols under solvent-free condition

21Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Acetophenone reacted with a series of aromatic aldehydes with grinding under catalysis of a double-component solid base system consisting of NaOH and K2CO3 to furnish highly chemoselectively 1,2,3,4,5-pentasubstituted cyclohexanols in 80-95% yield, and their composition and structure are identified by spectral technologies and single crystal X-ray diffraction analysis, and a possible mechanism of the formation was suggested. © 2006 Elsevier Ltd. All rights reserved.

Cite

CITATION STYLE

APA

Luo, X., & Shan, Z. (2006). Highly chemoselective synthesis of 1,2,3,4,5-pentasubstituted cyclohexanols under solvent-free condition. Tetrahedron Letters, 47(32), 5623–5627. https://doi.org/10.1016/j.tetlet.2006.06.037

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free