Literature DB >> 20381018

Studies on the Zn(II)-mediated electrophilic selenocyclization and elimination of 3,4-O-isopropylidene-protected hydroxyalkenyl sulfides: synthesis of a 2-phenylselenenyl glycal.

Omar Boutureira1, Miguel A Rodríguez, Yolanda Díaz, M Isabel Matheu, Sergio Castillón.   

Abstract

Herein, we describe a mild and efficient Zn(II)-mediated electrophilic selenocyclization reaction of readily available and stable 3,4-O-isopropylidene-protected hydroxyalkenyl sulfides to 2-deoxy-2-phenylselenenyl-1-thio-glycosides. This material was transformed into a 2-phenylselenenyl glycal in a controlled manner using an activation-elimination sequence. (c) 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20381018     DOI: 10.1016/j.carres.2010.03.001

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


  2 in total

1.  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

2.  19F labelled glycosaminoglycan probes for solution NMR and non-linear (CARS) microscopy.

Authors:  Marcelo A Lima; Renan P Cavalheiro; Gustavo M Viana; Maria C Z Meneghetti; Timothy R Rudd; Mark A Skidmore; Andrew K Powell; Edwin A Yates
Journal:  Glycoconj J       Date:  2016-08-15       Impact factor: 2.916

  2 in total

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