Literature DB >> 17939718

Tandem acetalation-acetylation of sugars and related derivatives with enolacetates under solvent-free conditions.

Debaraj Mukherjee1, Bhahwal Ali Shah, Pankaj Gupta, Subhash Chandra Taneja.   

Abstract

Molecular iodine catalyzes acetalation and acetylation of reducing sugars and sugar glycosides with stoichiometric amounts of enol acetates under solvent-free conditions, thereby facilitating the synthesis of various types of orthogonally protected sugar derivatives in short time and good yields. The outcome of the reaction can be controlled by variation in temperature. Thus at lower temperature, it is possible to obtain the acetonide acetate as a single product whereas peracetate is the major product at higher temperature.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17939718     DOI: 10.1021/jo070363i

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  A general metal-free approach for the stereoselective synthesis of C-glycals from unactivated alkynes.

Authors:  Shekaraiah Devari; Manjeet Kumar; Ramesh Deshidi; Masood Rizvi; Bhahwal Ali Shah
Journal:  Beilstein J Org Chem       Date:  2014-11-12       Impact factor: 2.883

2.  Regioselective Dehydration of Sugar Thioacetals under Mild Conditions.

Authors:  Rachel Szpara; Alexander Goyder; Michael J Porter; Helen C Hailes; Tom D Sheppard
Journal:  Org Lett       Date:  2021-03-17       Impact factor: 6.005

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.