Literature DB >> 16630601

Novel glycosylation methods and their application to natural products synthesis.

Kazunobu Toshima1.   

Abstract

In this short review article, several glycosylation methods that were developed in our laboratories, including stereocontrolled glycosylation using 2,6-anhydro-2,6-dideoxy-2,6-dithio sugars for obtaining 2,6-dideoxy glycosides, C-glycosylation employing unprotected sugars, environmentally benign glycosylation utilizing heterogeneous solid acids and ionic liquids, are recounted. In addition, representative and significant applications of these methods to the synthesis of complex natural products are described.

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Year:  2006        PMID: 16630601     DOI: 10.1016/j.carres.2006.03.012

Source DB:  PubMed          Journal:  Carbohydr Res        ISSN: 0008-6215            Impact factor:   2.104


  3 in total

1.  Recent Advances in Transition Metal-Catalyzed Glycosylation.

Authors:  Matthew J McKay; Hien M Nguyen
Journal:  ACS Catal       Date:  2012-06-14       Impact factor: 13.084

2.  Novel galactosyl donor with 2-naphthylmethyl (NAP) as the non participating group at C-2 position: Efficient synthesis of alpha-galactosyl ceramide.

Authors:  Sirajud D Khaja; Vipin Kumar; Misbah Ahmad; Jun Xue; Khushi L Matta
Journal:  Tetrahedron Lett       Date:  2010-08-18       Impact factor: 2.415

3.  Highly reactive 2-deoxy-2-iodo-d-allo and d-gulo pyranosyl sulfoxide donors ensure β-stereoselective glycosylations with steroidal aglycones.

Authors:  Jordi Mestre; David Collado; David Benito-Alifonso; Miguel A Rodríguez; M Isabel Matheu; Yolanda Díaz; Sergio Castillón; Omar Boutureira
Journal:  RSC Adv       Date:  2018-08-24       Impact factor: 4.036

  3 in total

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