Issue 16, 1993

Synthesis of 2,3-Di-O-palmitoyl-α,α-trehalose via a novel tri-protected trehalose intermediate

Abstract

2′-,3′–;4,6;4′,6′-Tri-O-cyclohexylidene-α,α-trehalose 4 is prepared from α,α-trehalose, regioselectively acylated at C-2 with palmitate; after further acylation with palmitate at C-3, deacetalisation gives 2,3-di-O-palmitoyl-α,α-trehalose 2.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 1292-1293

Synthesis of 2,3-Di-O-palmitoyl-α,α-trehalose via a novel tri-protected trehalose intermediate

P. A. Wallace and D. E. Minnikin, J. Chem. Soc., Chem. Commun., 1993, 1292 DOI: 10.1039/C39930001292

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