Literature DB >> 9249149

A new entry to glycosylamines.

F L Merchán1, P Merino, T Tejero.   

Abstract

A new procedure for the introduction of a nitrogen atom into the anomeric centre leading to glycosylamines is described. The new reaction consisting of the condensation of a furanose with a hydroxylamine in the presence of a Lewis acid occurs with a complete degree of diastereoselectivity.

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Year:  1997        PMID： 9249149     DOI： 10.1023/a:1018559720428

Source DB:  PubMed          Journal:  Glycoconj J        ISSN： 0282-0080            Impact factor:   2.916


  2 in total

1.  Fmoc-protected, glycosylated asparagines potentially useful as reagents in the solid-phase synthesis of N-glycopeptides.

Authors:  L Urge; L Otvos; E Lang; K Wroblewski; I Laczko; M Hollosi
Journal:  Carbohydr Res       Date:  1992-11-04       Impact factor: 2.104

Review 2.  The use of inhibitors in the study of glycosidases.

Authors:  P Lalégerie; G Legler; J M Yon
Journal:  Biochimie       Date:  1982 Nov-Dec       Impact factor: 4.079
  2 in total
  2 in total

1.  Total synthesis of (+)-sieboldine a: evolution of a pinacol-terminated cyclization strategy.

Authors:  Stephen M Canham; David J France; Larry E Overman
Journal:  J Org Chem       Date:  2012-06-26       Impact factor: 4.354

2.  Total synthesis of (+)-sieboldine A.

Authors:  Stephen M Canham; David J France; Larry E Overman
Journal:  J Am Chem Soc       Date:  2010-06-16       Impact factor: 15.419
  2 in total

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