Literature DB >> 18491016

Conformationally armed glycosyl donors: reactivity quantification, new donors and one pot reactions.

Christian Marcus Pedersen1, Lavinia G Marinescu, Mikael Bols.   

Abstract

The relative reactivity of conformationally armed thioglycosides is quantified.

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Year:  2008        PMID： 18491016     DOI： 10.1039/b801305e

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


  13 in total

1.  Stereoselectivity of Conformationally Restricted Glucosazide Donors.

Authors:  Stefan van der Vorm; Herman S Overkleeft; Gijsbert A van der Marel; Jeroen D C Codée
Journal:  J Org Chem       Date:  2017-04-25       Impact factor: 4.354

Review 2.  Automated Chemical Oligosaccharide Synthesis: Novel Approach to Traditional Challenges.

Authors:  Matteo Panza; Salvatore G Pistorio; Keith J Stine; Alexei V Demchenko
Journal:  Chem Rev       Date:  2018-06-28       Impact factor: 60.622

3.  Comparison of the armed/disarmed building blocks of the D-gluco and D-glucosamino series in the context of chemoselective oligosaccharide synthesis.

Authors:  Teerada Kamkhachorn; Archana R Parameswar; Alexei V Demchenko
Journal:  Org Lett       Date:  2010-07-02       Impact factor: 6.005

Review 4.  Superarmed and superdisarmed building blocks in expeditious oligosaccharide synthesis.

Authors:  Hemali D Premathilake; Alexei V Demchenko
Journal:  Top Curr Chem       Date:  2011

5.  Superarming of glycosyl donors by combined neighboring and conformational effects.

Authors:  Mads Heuckendorff; Hemali D Premathilake; Papapida Pornsuriyasak; Anders Ø Madsen; Christian M Pedersen; Mikael Bols; Alexei V Demchenko
Journal:  Org Lett       Date:  2013-09-05       Impact factor: 6.005

Review 6.  Synthesis and Glycosidation of Anomeric Halides: Evolution from Early Studies to Modern Methods of the 21st Century.

Authors:  Yashapal Singh; Scott A Geringer; Alexei V Demchenko
Journal:  Chem Rev       Date:  2022-06-08       Impact factor: 72.087

7.  Conformationally superarmed S-ethyl glycosyl donors as effective building blocks for chemoselective oligosaccharide synthesis in one pot.

Authors:  Mithila D Bandara; Jagodige P Yasomanee; Nigam P Rath; Christian M Pedersen; Mikael Bols; Alexei V Demchenko
Journal:  Org Biomol Chem       Date:  2017-01-18       Impact factor: 3.876

Review 8.  First principles insight into the alpha-glucan structures of starch: their synthesis, conformation, and hydration.

Authors:  Iben Damager; Søren Balling Engelsen; Andreas Blennow; Birger Lindberg Møller; Mohammed Saddik Motawia
Journal:  Chem Rev       Date:  2010-04-14       Impact factor: 60.622

9.  Synthesis of lipid-linked arabinofuranose donors for glycosyltransferases.

Authors:  Matthew B Kraft; Mario A Martinez Farias; Laura L Kiessling
Journal:  J Org Chem       Date:  2013-02-07       Impact factor: 4.354

10.  Superarming common glycosyl donors by simple 2-O-benzoyl-3,4,6-tri-O-benzyl protection.

Authors:  Hemali D Premathilake; Laurel K Mydock; Alexei V Demchenko
Journal:  J Org Chem       Date:  2010-02-19       Impact factor: 4.354
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