Literature DB >> 25957213

Synthesis of lemonose derivatives: methyl 4-amino-3-O,4-N-carbonyl-2,4,6-trideoxy-3-C-methyl-α-l-lyxo-pyranoside and its phenyl thioglycoside.

Alicia C Briegel1, Adrienne K Cummings1, Garry R Smith1, Matthew D Doroski1, Walter J Boyko1, Nicholas A Piro1, W Scott Kassel1, Robert M Giuliano2.   

Abstract

Lemonose is a component of the antibiotic lemonomycin and other antibiotics and natural products. Three routes to the synthesis of the title compound, a protected, desmethyl derivative of lemonose, from l-rhamnose or its glycal, were investigated based on electrophilic cyclization, epoxidation-ring opening, and deoxygenation of an intermediate that was used in the synthesis of the amino sugar callipeltose. The deoxygenation route was successful and it provided the title compound, which was then converted to a phenyl thioglycoside.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Callipeltose; Lemonomycin; Lemonose

Mesh:

Substances:

Year:  2015        PMID: 25957213     DOI: 10.1016/j.carres.2015.03.006

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


  2 in total

1.  Cooperative Involvement of Glycosyltransferases in the Transfer of Amino Sugars during the Biosynthesis of the Macrolactam Sipanmycin by Streptomyces sp. Strain CS149.

Authors:  Mónica G Malmierca; Ignacio Pérez-Victoria; Jesús Martín; Fernando Reyes; Carmen Méndez; Carlos Olano; José A Salas
Journal:  Appl Environ Microbiol       Date:  2018-08-31       Impact factor: 4.792

2.  De Novo Synthesis of an l-Lemonose Thioglycoside Donor from d-Threonine.

Authors:  Eric D Huseman; Steven D Townsend
Journal:  Tetrahedron Lett       Date:  2021-04-22       Impact factor: 2.032

  2 in total

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