Literature DB >> 22683886

A dramatic concentration effect on the stereoselectivity of N-glycosylation for the synthesis of 2'-deoxy-β-ribonucleosides.

Fei Yang1, Yugen Zhu, Biao Yu.   

Abstract

A dramatic concentration effect on the stereoselectivity of N-glycosylation, which is attributable to a low-concentration-facilitated remote-participation, has been disclosed, leading to convenient synthesis of the 2'-deoxy-β-ribonucleosides of biological significance.

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Year:  2012        PMID： 22683886     DOI： 10.1039/c2cc33155a

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  3 in total

1.  Participation of alkoxy groups in reactions of acetals: violation of the reactivity/selectivity principle in a Curtin-Hammett kinetic scenario.

Authors:  Angie Garcia; Jillian R Sanzone; K A Woerpel
Journal:  Angew Chem Int Ed Engl       Date:  2015-08-19       Impact factor: 15.336

2.  2,6-Di-chloro-9-(2',3',5'-tri-O-acetyl-β-d-ribo-furanos-yl)-9H-purine.

Authors:  Irina Novosjolova; Dmitrijs Stepanovs; Erika Bizdēna; Anatoly Mishnev; Māris Turks
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2014-01-04

3.  Cladribine Analogues via O⁶-(Benzotriazolyl) Derivatives of Guanine Nucleosides.

Authors:  Sakilam Satishkumar; Prasanna K Vuram; Siva Subrahmanyam Relangi; Venkateshwarlu Gurram; Hong Zhou; Robert J Kreitman; Michelle M Martínez Montemayor; Lijia Yang; Muralidharan Kaliyaperumal; Somesh Sharma; Narender Pottabathini; Mahesh K Lakshman
Journal:  Molecules       Date:  2015-10-09       Impact factor: 4.411
  3 in total

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